During early respiratory system development, the foregut endoderm gives rise to the tracheal and lung cell progenitors. Through branching morphogenesis, and in coordination with vascular development, a tree-like structure of epithelial tubules forms and differentiates to produce the airways and alveoli. Recent studies have implicated the fibroblast growth factor, sonic hedgehog, bone morphogenetic protein, retinoic acid and Wnt signaling pathways, and various transcription factors in regulating the initial stages of lung development. However, the precise roles of these molecules and how they interact in the developing lung is subject to debate. Here, we review early stages in lung development and highlight questions and controversies regarding their molecular regulation.

Introduction

The basic design of the mammalian respiratory system, referred to here as the trachea and lung, is that of a tree of epithelial tubules in which air is cleaned, humidified and delivered to numerous alveolar units closely apposed to blood vessels, where the circulating blood is oxygenated.

The respiratory system arises from the ventral foregut endoderm. The process initiates with the establishment of respiratory cell fate in the primitive foregut. This is followed by the development of a tree-like system of epithelial tubules and vascular structures (see Fig. 1), which ultimately gives rise to the mature airways and alveoli. The foregut endoderm differentiates into various epithelial cell types, which line the inner surface of the developing lung and trachea. The lung mesenchyme originates from the lateral plate mesoderm and gives rise to multiple components of the lung, including its connective tissue, endothelial cell precursors, the smooth muscle that surrounds airways and blood vessels, the cartilage of the trachea, the lymphatics, and the mesothelial cells that cover the outer surface of the lung, the pleura. The lung vasculature forms, in part, by migration of blood vessels from the aortic arches and from the left atrium to the lung(angiogenesis). Blood vessels also develop by vasculogenesis in the lung mesenchyme near developing epithelial buds; a rudimentary capillary network initially forms and expands, and later connects to the larger vessels to give rise to the lung vasculature (Wood et al., 1997; Demello et al.,1997; Gebb and Shannon,2000). There is evidence that, during organogenesis, blood vessels serve as a source of inductive signals to the epithelium(Lammert et al., 2001; Matsumoto et al., 2001). However, the role of the vasculature in epithelial patterning has still to be clearly demonstrated in the developing lung.

The mechanisms that control respiratory system formation have been the subjects of an increasing number of studies. This review focuses on our current knowledge of the molecular regulation of early lung development. Topics discussed here include lung endodermal specification, lung primordium formation, and the regulation of the initial stages of branching morphogenesis and differentiation in the embryonic lung. We address questions such as `when and how is respiratory cell fate established?', `how do lung buds form?', `how are stereotypical patterns of airway branching and cellular diversity generated in the developing lung?' and `which pathways and targets are key to these processes?'. Most of what is described refers to mouse lung development because of the genetic data available(Table 1). Lung vascular development and later events, such as sacculation and alveoli formation, are not discussed in this review (for reviews, see Pauling and Vu, 2004; Williams, 2003; Bourbon et al., 2005).

Table 1.

Examples of mutations in mouse giving a reported lung and/or tracheal phenotype

Gene symbolGene nameExpression patternPhenotypeReference
Signaling molecule     
Egfr Epidermal growth factor receptor Epithelium and mesenchyme Impaired branching and deficient alveolization Miettinen et al. (1997
Fgf18 Fibroblast growth factor 18 Mesenchyme Deficient alveolization Usui et al. (2004
Fgf9 Fibroblast growth factor 9 Epithelium and pleura Impaired branching, reduced mesenchyme Colvin et al. (2001
Grem1 Gremlin 1 Epithelium and mesenchyme Deficient alveolization Michos et al. (2004
Hip1 Huntingtin-interacting protein 1 Mesenchyme Impaired branching Chuang et al. (2003
Shh Sonic hedgehog Epithelium Impaired branching, tracheoesophageal fistula Litingtung et al. (1998
Tgfb3 Transforming growth factor, β3 Epithelium and pleura Impaired branching Kaartinen et al. (1995
Wnt7b Wingless-related MMTV integration site 7B Epithelium Vascular defect, reduced mesenchyme Shu et al. (2002
Catnnb1 β-Catenin Epithelium Impaired branching, proximal/distal specification Mucenski et al. (2003
Ltbp4 Latent transforming growth factor β binding protein 4 Not reported Pulmonary emphysema Sterner-Kock et al. (2002
Wnt5a Wingless-related MMTV integration site 5A Mesenchyme and epithelium Increased branching, tracheal defect Li et al. (2002
Fgf10 Fibroblast growth factor 10 Mesenchyme Lung agenesis Sekine et al. (1999
Fgfr2b Fibroblast growth factor receptor 2b Epithelium Lung agenesis De Moerlooze et al. (2000
Fgf8 Fibroblast growth factor 8 Not reported Right pulmonary isomerism Fischer et al. (2002
Acvr2b Activin receptor IIB Not reported Right pulmonary isomerism Oh and Li (1997
Nodal Nodal Not reported Right pulmonary isomerism Lowe et al. (2001
Lefty1 Left right determination factor 1 Not reported Left pulmonary isomerism Meno et al. (1998
Traf4 Tnf receptor associated factor 4 Not reported Tracheal defect Shiels et al. (2000
Fgfr3/Fgfr4 Fibroblast growth factor receptor 3/4 Epithelium and mesenchyme Deficient alveolization Weinstein et al. (1998
Nog Noggin Mesenchyme Lobation defect Weaver et al. (2003
Transcription factor     
Cebpa CCAAT/enhancer binding protein (C/EBP), α Epithelium Hyperproliferation of type II cells Sugahara et al. (2001
Foxa1/Foxa2 Forkhead box A1/A2 Epithelium Impaired branching, reduced smooth muscle Wan et al. (2005
Foxf1a Forkhead box F1a Mesenchyme Impaired branching, lobation defect Lim et al. (2002
Hoxa5 Homeobox A5 Mesenchyme Impaired branching, tracheal defect Aubin et al. (1997
Klf2 Kruppel-like factor 2 (lung) Not reported Impaired sacculation Wani et al. (1999
Mycn Neuroblastoma myc-related oncogene 1 Epithelium Impaired branching Moens et al. (1992
Trp63 Transformation-related protein 63 Epithelium Tracheobronchial defect Daniely et al. (2004
Titf1 Thyroid transcription factor 1 Epithelium Loss of distal lung fate, impaired branching, tracheoesophageal fistula Kimura et al. (1996
Nfib Nuclear factor I/B Epithelium and mesenchyme Sacculation defect Steele-Perkins et al. (2005
Sox11 SRY-box-containing gene 11 Epithelium Hypoplastic lung Sock et al. (2004
Tcf21 Transcription factor 21 (Pod1) Mesenchyme Impaired branching Quaggin et al. (1999
Rarb/Rara Retinoic acid receptor α/β Epithelium and mesenchyme Left lung agenesis and right lung hypoplasia Mendelsohn et al. (1994
Pitx2 Paired-like homeodomain transcription factor 2 Mesenchyme Right pulmonary isomerism Lin et al. (1999
Foxj1 Forkhead box J1 Epithelium Left-right asymmetry, loss of ciliated cells Brody et al. (2000
Gata6 GATA-binding protein 6 Epithelium Impaired sacculation Yang et al. (2002
Gli2/Gli3 GLI-Kruppel family member GLI2/GLI3 Mesenchyme Lung agenesis Motoyama et al. (1998
Ascl1 Achaete-scute complex homolog-like 1 Neuroendocrine cells Loss of neuroendocrine cells Ito et al. (2000
Others     
Eln Elastin Mesenchyme Deficient alveolization Wendel et al. (2000
Lmnb1 Lamin B1 Epithelium and mesenchyme Deficient alveolization Vergnes et al. (2004
Lama5 Laminin α5 Epithelium and pleura Defective lobation Nguyen et al. (2002
Pcaf p300/CBP-associated factor Epithelium and mesenchyme Defective proximal and distal epithelial cell differentiation Shikama et al. (2003
Adam17 A disintegrin and metallopeptidase domain 17 Epithelium Impaired epithelial differentiation, impaired branching Zhao et al. (2001
    Peschon et al. (1998
Crh Corticotropin releasing hormone Epithelium Defective epithelial and mesenchymal maturation Muglia et al. (1999
Pthlh Parathyroid hormone-like peptide Epithelium Deficient alveolization Rubin et al. (2004
Itga3 Integrin α3 Epithelium Impaired branching Kreidberg et al. (1996
Cutl1 Cut-like 1 Epithelium Impaired epithelial differentiation Ellis et al. (2001
Gene symbolGene nameExpression patternPhenotypeReference
Signaling molecule     
Egfr Epidermal growth factor receptor Epithelium and mesenchyme Impaired branching and deficient alveolization Miettinen et al. (1997
Fgf18 Fibroblast growth factor 18 Mesenchyme Deficient alveolization Usui et al. (2004
Fgf9 Fibroblast growth factor 9 Epithelium and pleura Impaired branching, reduced mesenchyme Colvin et al. (2001
Grem1 Gremlin 1 Epithelium and mesenchyme Deficient alveolization Michos et al. (2004
Hip1 Huntingtin-interacting protein 1 Mesenchyme Impaired branching Chuang et al. (2003
Shh Sonic hedgehog Epithelium Impaired branching, tracheoesophageal fistula Litingtung et al. (1998
Tgfb3 Transforming growth factor, β3 Epithelium and pleura Impaired branching Kaartinen et al. (1995
Wnt7b Wingless-related MMTV integration site 7B Epithelium Vascular defect, reduced mesenchyme Shu et al. (2002
Catnnb1 β-Catenin Epithelium Impaired branching, proximal/distal specification Mucenski et al. (2003
Ltbp4 Latent transforming growth factor β binding protein 4 Not reported Pulmonary emphysema Sterner-Kock et al. (2002
Wnt5a Wingless-related MMTV integration site 5A Mesenchyme and epithelium Increased branching, tracheal defect Li et al. (2002
Fgf10 Fibroblast growth factor 10 Mesenchyme Lung agenesis Sekine et al. (1999
Fgfr2b Fibroblast growth factor receptor 2b Epithelium Lung agenesis De Moerlooze et al. (2000
Fgf8 Fibroblast growth factor 8 Not reported Right pulmonary isomerism Fischer et al. (2002
Acvr2b Activin receptor IIB Not reported Right pulmonary isomerism Oh and Li (1997
Nodal Nodal Not reported Right pulmonary isomerism Lowe et al. (2001
Lefty1 Left right determination factor 1 Not reported Left pulmonary isomerism Meno et al. (1998
Traf4 Tnf receptor associated factor 4 Not reported Tracheal defect Shiels et al. (2000
Fgfr3/Fgfr4 Fibroblast growth factor receptor 3/4 Epithelium and mesenchyme Deficient alveolization Weinstein et al. (1998
Nog Noggin Mesenchyme Lobation defect Weaver et al. (2003
Transcription factor     
Cebpa CCAAT/enhancer binding protein (C/EBP), α Epithelium Hyperproliferation of type II cells Sugahara et al. (2001
Foxa1/Foxa2 Forkhead box A1/A2 Epithelium Impaired branching, reduced smooth muscle Wan et al. (2005
Foxf1a Forkhead box F1a Mesenchyme Impaired branching, lobation defect Lim et al. (2002
Hoxa5 Homeobox A5 Mesenchyme Impaired branching, tracheal defect Aubin et al. (1997
Klf2 Kruppel-like factor 2 (lung) Not reported Impaired sacculation Wani et al. (1999
Mycn Neuroblastoma myc-related oncogene 1 Epithelium Impaired branching Moens et al. (1992
Trp63 Transformation-related protein 63 Epithelium Tracheobronchial defect Daniely et al. (2004
Titf1 Thyroid transcription factor 1 Epithelium Loss of distal lung fate, impaired branching, tracheoesophageal fistula Kimura et al. (1996
Nfib Nuclear factor I/B Epithelium and mesenchyme Sacculation defect Steele-Perkins et al. (2005
Sox11 SRY-box-containing gene 11 Epithelium Hypoplastic lung Sock et al. (2004
Tcf21 Transcription factor 21 (Pod1) Mesenchyme Impaired branching Quaggin et al. (1999
Rarb/Rara Retinoic acid receptor α/β Epithelium and mesenchyme Left lung agenesis and right lung hypoplasia Mendelsohn et al. (1994
Pitx2 Paired-like homeodomain transcription factor 2 Mesenchyme Right pulmonary isomerism Lin et al. (1999
Foxj1 Forkhead box J1 Epithelium Left-right asymmetry, loss of ciliated cells Brody et al. (2000
Gata6 GATA-binding protein 6 Epithelium Impaired sacculation Yang et al. (2002
Gli2/Gli3 GLI-Kruppel family member GLI2/GLI3 Mesenchyme Lung agenesis Motoyama et al. (1998
Ascl1 Achaete-scute complex homolog-like 1 Neuroendocrine cells Loss of neuroendocrine cells Ito et al. (2000
Others     
Eln Elastin Mesenchyme Deficient alveolization Wendel et al. (2000
Lmnb1 Lamin B1 Epithelium and mesenchyme Deficient alveolization Vergnes et al. (2004
Lama5 Laminin α5 Epithelium and pleura Defective lobation Nguyen et al. (2002
Pcaf p300/CBP-associated factor Epithelium and mesenchyme Defective proximal and distal epithelial cell differentiation Shikama et al. (2003
Adam17 A disintegrin and metallopeptidase domain 17 Epithelium Impaired epithelial differentiation, impaired branching Zhao et al. (2001
    Peschon et al. (1998
Crh Corticotropin releasing hormone Epithelium Defective epithelial and mesenchymal maturation Muglia et al. (1999
Pthlh Parathyroid hormone-like peptide Epithelium Deficient alveolization Rubin et al. (2004
Itga3 Integrin α3 Epithelium Impaired branching Kreidberg et al. (1996
Cutl1 Cut-like 1 Epithelium Impaired epithelial differentiation Ellis et al. (2001

From gut to lungs: the origin of the respiratory system

Foregut morphogenesis and establishment of endodermal cell fate

Following gastrulation (embryonic day E7.5 in mice), the definitive endoderm undergoes complex morphogenetic movements that ultimately lead to the formation of the primitive gut tube. The foregut represents the most anterior(cranial) region of this tube, while the midgut and hindgut are located at progressively more posterior regions, towards the caudal end of the embryo(Wells and Melton, 1999). Transcription factor genes such as Foxa1, Foxa2, Gata4 and Gata6, which are expressed early in the endoderm, are crucial for the survival, differentiation and morphogenesis of the foregut(Kuo et al., 1997; Morrisey et al., 1998; Ang and Rossant, 1994; Wan et al., 2005). By E8.0-9.5, the local expression of transcription factors along the anteroposterior (AP) axis of the gut endoderm marks organ-specific domains (or fields; see Fig. 1A). For example, the homeodomain protein gene Nkx2.1 [also known as thyroid transcription factor 1 (Titf1) or T/EBP] is expressed in the thyroid and respiratory fields (Kimura et al., 1996), Hex (hematopoietically expressed homeobox) is expressed in the thyroid and liver fields(Martinez Barbera et al.,2000), and the Pdx1 (pancreas-duodenal-associated homeobox gene) is expressed in the pancreatic and duodenal fields(Offield et al., 1996). In addition, morphogenetic movements foster dynamic interactions between the endoderm and neighboring structures, such as the heart, notochord or the septum transversum (the mesodermal cells that give rise to the diaphragm). Exposure of the endoderm to diffusible signals from these structures at crucial developmental windows is essential for endodermal cell fate specification (Kumar and Melton,2003; Bort et al.,2004).

Fibroblast growth factor 4 (Fgf4), bone morphogenetic protein 2 (Bmp2) and retinoic acid (RA) are among the signals that confer AP identity to the early endoderm. They render the endoderm competent to respond to signals from the adjacent mesoderm or from nearby structures to initiate morphogenesis(Tiso et al., 2002; Stafford and Prince, 2002; Wells and Melton, 2000). In zebrafish, disrupted RA signaling during gastrulation results in the loss of liver and pancreatic (posterior) fates, while thyroid and pharynx (anterior)fates remain unaltered. Conversely, excess RA induces hepatic and pancreatic cell fates at more anterior domains(Stafford and Prince, 2002). In mice and rats, RA signaling initiates soon after gastrulation(Rossant et al., 1991), but does not seem to be as crucial for foregut AP identity as it is in the zebrafish.

Fig. 1.

Key events during early development of the mouse respiratory system.(A) The foregut (gray tube) is initially specified into organ-specific domains along its anteroposterior (AP) axis, which later give rise to the thyroid (Th), thymus, trachea (Tr), lung (Lu), liver (Li) and pancreas (Pa). The respiratory progenitors (Tr, Lu) arise from the ventral foregut endoderm,which is posterior to the thyroid but anterior to the liver and to the pancreatic fields. Lung and tracheal progenitors are identified collectively at E9.0 by Nkx2.1 expression (purple), which also labels the thyroid.(B) At E9.5, two endodermal lung buds (black arrows) are induced from the ventral-lateral aspect of the foregut, which then invade the adjacent mesoderm and elongate to form the primary buds (red arrows) of the right and left lung (V-D, ventral-dorsal axis). (C) With primary lung bud formation, the tracheal (Tr) primordium forms ventrally and separates from the dorsal foregut, the primitive esophagus (Es), in a poorly understood process that is possibly initiated by growth of an ascending tracheoesophageal septum or by fusion of endodermal ridges from the lateral walls of the foregut(Zaw-Tun, 1982; Sutliff and Hutchins, 1994; Ioannides et al., 2002).(D) At ∼E10.5 (left), secondary buds arise as outgrowths from the primary lung buds at specific positions (red arrowheads; the epithelium is labeled by Fgfr2b). In the right lung (RLu), these buds later develop into separate lobes. At E11.5-12.0 (right), the left lung (LLu) has one lobe and RLu has four: the cranial (cr), medial (me), caudal (ca) and accessory(ac) lobes. From E10.5 to E16.5-E17.0, the epithelium undergoes branching morphogenesis, which involves bud outgrowth and elongation, dichotomous subdivisions and cleft formation at branching points. The process is reiterated over several generations of branches to form the respiratory(bronchial) tree. As this occurs, a proximodistal axis is established in the developing lung. Proximal regions (where buds are initially generated, yellow)stop branching and differentiate into proximal airways (bronchi), while distal regions (green) continue to branch and later give rise to the alveolar region of the lung. Numbers depict primary, secondary and tertiary generations of buds.

Fig. 1.

Key events during early development of the mouse respiratory system.(A) The foregut (gray tube) is initially specified into organ-specific domains along its anteroposterior (AP) axis, which later give rise to the thyroid (Th), thymus, trachea (Tr), lung (Lu), liver (Li) and pancreas (Pa). The respiratory progenitors (Tr, Lu) arise from the ventral foregut endoderm,which is posterior to the thyroid but anterior to the liver and to the pancreatic fields. Lung and tracheal progenitors are identified collectively at E9.0 by Nkx2.1 expression (purple), which also labels the thyroid.(B) At E9.5, two endodermal lung buds (black arrows) are induced from the ventral-lateral aspect of the foregut, which then invade the adjacent mesoderm and elongate to form the primary buds (red arrows) of the right and left lung (V-D, ventral-dorsal axis). (C) With primary lung bud formation, the tracheal (Tr) primordium forms ventrally and separates from the dorsal foregut, the primitive esophagus (Es), in a poorly understood process that is possibly initiated by growth of an ascending tracheoesophageal septum or by fusion of endodermal ridges from the lateral walls of the foregut(Zaw-Tun, 1982; Sutliff and Hutchins, 1994; Ioannides et al., 2002).(D) At ∼E10.5 (left), secondary buds arise as outgrowths from the primary lung buds at specific positions (red arrowheads; the epithelium is labeled by Fgfr2b). In the right lung (RLu), these buds later develop into separate lobes. At E11.5-12.0 (right), the left lung (LLu) has one lobe and RLu has four: the cranial (cr), medial (me), caudal (ca) and accessory(ac) lobes. From E10.5 to E16.5-E17.0, the epithelium undergoes branching morphogenesis, which involves bud outgrowth and elongation, dichotomous subdivisions and cleft formation at branching points. The process is reiterated over several generations of branches to form the respiratory(bronchial) tree. As this occurs, a proximodistal axis is established in the developing lung. Proximal regions (where buds are initially generated, yellow)stop branching and differentiate into proximal airways (bronchi), while distal regions (green) continue to branch and later give rise to the alveolar region of the lung. Numbers depict primary, secondary and tertiary generations of buds.

When and how is lung cell fate specified in the foregut?

The specification of the liver and pancreas has been extensively investigated (Rossi et al.,2001; Kumar and Melton,2003). By contrast, relatively fewer studies have focused on the lung. Lineage analysis suggests that the progenitor cells of the trachea and proximal lung differ in origin from those that will form the distal region of the lung (Perl et al., 2002). Precisely when respiratory cell fate is established in the foregut endoderm is still unclear. Respiratory progenitors are first visualized by in situ hybridization as a group of Nkx2.1-expressing endodermal cells in the prospective lung/tracheal region of the foregut, at ∼E9(Minoo et al., 1999). Nkx2.1 transcripts have been reported by RT-PCR to be present in the foregut as early as E8-8.5 (eight-somite stage)(Serls et al., 2005). These signals, however, probably originate from the thyroid primordium, as the thyroid starts to develop at least 1 day before the lung(Lazzaro et al., 1991). The surfactant-associated protein C (Sftpc) gene is the most specific marker of lung epithelial cell lineage, but its expression is consistently detected only by E10-10.5, after the primary buds form(Wert et al., 1993).

Studies in mouse foregut cultures strongly indicate that Fgfs emanating from the adjacent heart influence the AP fate of the ventral foregut endoderm in a concentration-dependent manner. A model of foregut specification has been proposed, in which different thresholds of Fgfs pattern the endoderm into different foregut derivatives, including the liver and lung(Fig. 2A). If cultured alone,the endoderm adopts a `default' pancreatic fate; adding increasing amounts of cardiac mesoderm or Fgf2 to the endoderm results first in induction of liver,and then of lung or thyroid fates (Rossi et al., 2001; Serls et al.,2005; Jung et al.,1999). In this system, the induction of lung cell fate appears to involve Fgfr4 signaling (Serls et al.,2005). Lung development, however, is apparently normal in Fgfr4-null mice (Weinstein et al., 1998). Currently, there is no evidence that sonic hedgehog(Shh) or Bmps, which are present in the foregut, are involved in lung endoderm specification. In summary, lung specification is likely to depend on signaling molecules, such as Fgfs from the heart, and local transcription factors that have yet to be identified.

Nkx2.1 and distal lung development

Although Nkx2.1 is the earliest known marker of the presumptive respiratory region, Nkx2.1-null mutant mice do have lungs(Minoo et al., 1999). These lungs, however, are highly abnormal and consist of two main bronchi, which give rise to cystic structures, lined by columnar cells with scattered cilia -features that are reminiscent of those found in proximal airways. Strikingly,marker analysis shows that the epithelium fails to express any of the surfactant-protein genes typically found in the normal distal lung. Whether distal lung progenitors are specified but not maintained in these mice cannot be determined without the identification of additional early markers of lung cell fate. Besides Nkx2.1, no other early marker is currently available. The presence of relatively preserved features of proximal differentiation in Nkx2.1-null mutants suggests that Nkx2.1may not be crucial for the developmental program of progenitor cells of the proximal lung (Minoo et al.,1999).

Fig. 2.

Molecular regulation of initial events in lung and tracheal development. (A) The developing mouse foregut from embryonic day(E) 8.0 to E9.0. (a) The Foxa and Gata transcription factors genes (yellow)are involved in early events, such as foregut (Fg) tube closure and establishing endodermal competence. (b,c) A model of foregut specification, in which increasing thresholds of Fgfs (purple), emanating from the heart (Ht),specify the ventral foregut endoderm into liver (Li) (blue line) or into lung(Lu) and thyroid (Th) (red, Nkx2.1-expressing endoderm). [See text and Serls et al. (Serls et al.,2005) for details.] (B) Regulation of primary lung bud formation, based on data from mouse and chick (see text for details). Foregut mesoderm is shown in gray, endoderm in blue, and the endoderm of the prospective trachea and lung in red. Lung budding (red) results from mesodermal induction of Fgf10 and from activation of Fgfr2b signaling in the endoderm (indicated by a yellow bracket). Retinoic acid (RA) and Tbx genes (TBX4 in chicks) regulate Fgf10 expression. Gli2 and Gli3 are both required for primary lung bud formation, presumably via an unknown intermediate factor (X). Bmp4 is expressed in the ventral mesoderm at the lung field, where its role is unknown. (C) Trachea (Tr) formation from the ventral foregut and its separation from the dorsal gut tube (Es, primitive esophagus). A cross-section through the foregut shows dorsoventral (DV) differences in gene expression that probably influence this process. For example, mice deficient in Shh or Nkx2.1, which are normally present in the ventral foregut endoderm, show tracheoesophageal fistula (incomplete separation of the respiratory and digestive systems) (Minoo et al., 1999; Litingtung et al., 1998). This defect has been also associated with deficiencies in Foxf1 (Lim et al.,2002), Tbx4(Sakiyama et al., 2003) and RA (Dickman et al., 1997).

Fig. 2.

Molecular regulation of initial events in lung and tracheal development. (A) The developing mouse foregut from embryonic day(E) 8.0 to E9.0. (a) The Foxa and Gata transcription factors genes (yellow)are involved in early events, such as foregut (Fg) tube closure and establishing endodermal competence. (b,c) A model of foregut specification, in which increasing thresholds of Fgfs (purple), emanating from the heart (Ht),specify the ventral foregut endoderm into liver (Li) (blue line) or into lung(Lu) and thyroid (Th) (red, Nkx2.1-expressing endoderm). [See text and Serls et al. (Serls et al.,2005) for details.] (B) Regulation of primary lung bud formation, based on data from mouse and chick (see text for details). Foregut mesoderm is shown in gray, endoderm in blue, and the endoderm of the prospective trachea and lung in red. Lung budding (red) results from mesodermal induction of Fgf10 and from activation of Fgfr2b signaling in the endoderm (indicated by a yellow bracket). Retinoic acid (RA) and Tbx genes (TBX4 in chicks) regulate Fgf10 expression. Gli2 and Gli3 are both required for primary lung bud formation, presumably via an unknown intermediate factor (X). Bmp4 is expressed in the ventral mesoderm at the lung field, where its role is unknown. (C) Trachea (Tr) formation from the ventral foregut and its separation from the dorsal gut tube (Es, primitive esophagus). A cross-section through the foregut shows dorsoventral (DV) differences in gene expression that probably influence this process. For example, mice deficient in Shh or Nkx2.1, which are normally present in the ventral foregut endoderm, show tracheoesophageal fistula (incomplete separation of the respiratory and digestive systems) (Minoo et al., 1999; Litingtung et al., 1998). This defect has been also associated with deficiencies in Foxf1 (Lim et al.,2002), Tbx4(Sakiyama et al., 2003) and RA (Dickman et al., 1997).

Why the lack of Nkx2.1 has such a negative effect on branching morphogenesis is still unclear. It is possible that, normally, Nkx2.1 controls the expression of molecules that are important for epithelial-mesenchymal interactions. Indeed, collagen type IV and several integrins, which are required for epithelial-mesenchymal interactions, are absent or greatly reduced in the lung epithelium of Nkx2.1-null mice(Yuan et al., 2000).

These studies suggest that Nkx2.1 is essential for the developmental program of epithelial cells of the distal lung and that Nkx2.1 is required for expression of several lung markers, such as Sftpc(Kelly et al., 1996). Although the promoter region of Nkx2.1 has been studied, little is known about the cis-active regulatory sequences that direct Nkx2.1 expression to the lung (Pan et al.,2004).

Primary lung bud formation

Lung bud morphogenesis: the role of Fgf10 and Fgfr2b

In mice, lung primordial buds form at E9.5 (∼25-somite stage; Fig. 1). As determined by studies in Drosophila, the budding of the developing tracheal system is initiated by the expression of a Fgf ligand (branchless) at prospective sites of budding; this is followed by the local activation of a Fgf receptor (breathless) in the endoderm to induce budding(Sutherland et al., 1996). In mammals, signaling by Fgf10 and Fgfr2b is crucial for lung bud formation. Fgf10 is a chemotactic and proliferation factor for the endoderm(Bellusci et al., 1997b; Park et al., 1998). Deletion of either Fgf10 or Fgfr2b in mice results in lung agenesis and multiple abnormalities (De Moerlooze et al., 2000; Min et al.,1998; Sekine et al.,1999). The overlapping features of Fgf10- and Fgfr2b-null mutants confirm Fgfr2b as the major receptor for Fgf10. Interestingly, unlike Fgf10-null mutants, Fgfr2b-null mice form an underdeveloped lung bud that soon undergoes apoptosis(De Moerlooze et al., 2000). This has been attributed to Fgf10-mediated activation of Fgfr1b, a receptor that also binds to Fgf10, but with much lower affinity(Lu et al., 1999). It is thus not able to maintain lung epithelial survival and the lung morphogenetic program that is normally carried out by Fgf10 and Fgfr2b signaling. Although tracheal morphogenesis has been reported to be normal in Fgf10-null mice at birth, a recent analysis of Fgf10 heterozygous mice has revealed that the size and number of tracheal submucosal glands are significantly reduced (Rawlins and Hogan,2005). These structures develop postnatally from the tracheal epithelium and probably recapitulate the Fgf-dependent program of budding and branching seen in the embryonic lung.

What controls lung primordium positioning in the foregut tube?

Little is known about the genes that control the positioning of the lung primordium in the foregut or the boundaries of the Fgf10 domain in the foregut (Fig. 2B). There is evidence, however, that Fgf10 expression and bud formation in the lung field are crucially dependent on RA(Desai et al., 2004). RA synthesis and use are prominent throughout the E8.5-9.5 mouse foregut(Malpel et al., 2000). Yet,disruption of RA signaling in the foregut affects the lung most dramatically and leads to several abnormalities, including lung agenesis(Wilson et al., 1953; Mollard et al., 2000). Culturing E8.5 foregut explants in the presence of a RA receptor antagonist prevents lung buds from forming. In this model, RA selectively regulates Fgf10 where the lung and neighboring stomach form(Desai et al., 2004). This seems to involve signaling by RA receptor β in the mesoderm(Desai et al., 2006).

Gli and T-box (Tbx) transcription factors have been also implicated in the formation of the lung primordium. Gli1, Gli2 and Gli3 are transcriptional effectors of the Shh signaling pathway that are present in the foregut mesoderm and later in the lung mesenchyme(Hui et al., 1994). In Gli2/Gli3 double-null mice, lung and tracheal primordium never form;other foregut derivatives develop but are smaller than normal, and most embryos die by E10.5 (Motoyama et al.,1998). This phenotype is intriguing, as it is more severe than that of Shh-null mutants(Pepicelli et al., 1998), and also because there is no evidence that during development these Gli proteins are preferentially expressed in the lung field. Presumably Gli2 and Gli3 induce a currently unidentified mesodermal diffusible signal that is required for bud formation.

In chick embryos, Tbx4 and Fgf10 are co-expressed in the foregut mesoderm in the lung field in a domain that coincides with that of Nkx2.1 in the endoderm, except in its most anterior portion. Studies in ovo show that misexpression of Tbx4 induces ectopic Fgf10expression and ectopic buds that express Nkx 2.1 mRNA. Tbx4 and Fgf10 are not required to initiate Nkx.2.1 expression, but appear to play a role in defining the posterior boundary of Nkx2.1 and the lung primordium (Sakiyama et al.,2003). However, the genetic inactivation of Tbx4 in mice does not prevent lung bud formation(Naiche and Papaioannou,2003). The overlapping expression of Tbx2, Tbx3, Tbx4 and Tbx5 in the developing foregut and lung mesoderm suggests that these genes may have a redundant role in foregut and lung morphogenesis(Chapman et al., 1996).

RA, Fgf10, Gli2, Gli3, Tbx2, Tbx3 and Tbx4, discussed here, all have in common expression in the foregut mesoderm at the onset of lung development and a potential, or demonstrated, involvement in primary lung bud induction.

Making the respiratory tree

From E10.5-E17.0, the lung epithelium undergoes branching morphogenesis to form the respiratory (or bronchial) tree. This process has been extensively studied in the lung (see Table 1), but many questions and controversies about its molecular regulation remain unresolved.

Fgf10 acts as the signal that triggers secondary and subsequent budding, as it does during primary budding (Fig. 3A). This, however, remains to be rigorously tested by conditional inactivation of Fgf10. At least during the initial generation of branches, lung buds arise in a highly stereotypical fashion. It has been proposed that the expression pattern of branchless in the developing Drosophila trachea or Fgf10 in the lung is invariant within a three-dimensional grid and could be set by global regulators of axis formation, such as the Hox genes (Metzger and Krasnow, 1999). Indeed, several Hox family members are expressed in partially overlapping domains along the AP axis of the mouse developing lung (Bogue et al.,1996; Volpe et al.,1997; Aubin et al.,1997). However, the lack of dramatic changes in the AP axis of the lung in single or double Hox-null mutants suggests that the role of these genes in lung patterning is still unclear.

An intriguing, dynamic pattern of expression of the Sry-like HMG box transcription factor Sox2 in the developing lung and thyroid epithelium has led to the hypothesis that local downregulation of Sox2 may be required for commencement of bud morphogenesis. During lung branching morphogenesis, Sox2 is associated with the epithelium that is less morphogenetically active, and expression is lost at sites where nascent buds arise (Ishii et al.,1998). The role of Sox2 in the lung remains to be demonstrated;mice deficient in Sox2 die prior to organogenesis because of the inability of the stem cells to proliferate (Avilion et al., 2003).

Left-right asymmetry and branching

Left and right lungs are asymmetric, as is apparent by their distinct patterns of branching and by the different number of lobes on each side (lobes are morphological units of the lung that are covered by the visceral pleura). The number of lobes varies in different species. Murine lungs characteristically have one lobe on the left and four lobes on the right (see Fig. 1D). Asymmetry of the lung is dependent on left-right (LR) determinants. The process is part of an early global program of axis specification that is regulated by several Tgfb-related molecules, such as activin receptor 2, Lefty1, Lefty2 and growth differentiation factor 1, and by the bicoid type homeobox gene Pitx2(Oh and Li, 1997; Meno et al., 1998; Kitamura et al., 1999; Rankin et al., 2000; Lin et al., 1999). Disruption of these genes results in laterality defects in multiple organs. In the lung,these defects commonly manifest as isomerism, the presence of equal numbers of lobes (with either right or left pattern) on both sides(Table 1). Interestingly, most of these genes are expressed in the mouse foregut mesoderm only transiently(E8-8.5). Except for Pitx2, expression of LR determinants ceases by the time the lung primordium forms (E9.5). The relatively late appearance of Pitx2 has led to the hypothesis that this gene acts as an executor of early genetic programs that control asymmetry in different structures of the embryo (Kitamura et al.,1999). Among the three isoforms (a, b, c), only Pitx2c is asymmetrically expressed in the left lung. Pitx2-null mice show right pulmonary isomerism (four-lobed lungs bilaterally)(Kitamura et al., 1999). Thus,during normal development, Pitx2 could presumably influence gene expression in the left lung, allowing budding only at specific sites. By doing so, Pitx2 would generate a simpler pattern of branching (and lobation), characteristic of the left lung. How Pitx2 exerts its functions, and whether Pitx2and Fgf10 interact in the lung mesenchyme, are unknown. Only a limited number of Pitx2 targets have been reported, and they shed little light on these issues (Ganga et al., 2003).

Control of budding by sprouty and Shh

The exchange of signals between the growing bud and the surrounding mesenchyme establishes feedback responses that control the size and shape of the bud during branching. This is illustrated by the mechanisms that control Fgfr2b activity or Fgf10 expression by the sprouty (Spry) or the Shh pathways, respectively (Fig. 3B-D).

Spry genes encode a family of cysteine-rich proteins (there are four members in mice) that interact with crucial elements of the receptor tyrosine kinase Rtk-Ras-Erk/Mapk cascade and interfere with the intensity or timing of Rtk signaling by ligands such as Fgf and Egf(Kim and Bar-Sagi, 2004). In the mouse lung epithelial cell line MLE15, Spry2 inhibits Fgf10-Fgfr2 signaling by binding to Frs2 (fibroblast growth factor receptor substrate 2),Grb2 (growth factor receptor bound protein 2) and Raf (v-raf-leukemia viral oncogene 1), and by disassociating from Gap1 (GTPase-activating protein 1) and Shp2 (Src homology 2-containing phosphotyrosine phosphatase)(Tefft et al., 2002).

In the developing E11-12 mouse lung, Spry2 is expressed at the tips of the growing epithelial buds, while Spry4 is present in the surrounding distal lung mesenchyme. Spry2 is one of the earliest targets to be induced in the lung epithelium in response to Fgf10(Mailleux et al., 2001). By acting as a Fgf10-dependent inhibitor of Fgfr2b activity, Spry2 limits the proliferation or migration of the lung epithelium when buds are forming. This could be part of a mechanism to control the size of the bud or to stop bud formation and, ultimately, to inhibit branching morphogenesis. Consistent with this role, reducing Spry2 activity in lung organ cultures results in increased branching (Tefft et al.,1999), as also reported for the tracheal system of Drosophila in Spry mutants(Hacohen et al., 1998). Conversely, overexpression of Spry2 or misexpression of Spry4 in the distal lung epithelium of transgenic mice severely impairs branching (Mailleux et al.,2001; Perl et al.,2003).

Fig. 3.

Models of bud formation and proximodistal patterning in the developing lung. A developing lung bud during branching morphogenesis. Mesenchyme is depicted in gray and the epithelium in blue or red (distal bud). (A)Branching initiates with local Fgf10 expression in the distal mesenchyme. Fgf10 diffuses (yellow arrow) and binds locally to Fgfr2b(expressed throughout the lung epithelium) to activate signaling and induce a bud (white arrow). (B) As the bud elongates, Fgfr2b signaling induces expression of Spry2 (which negatively regulates Fgf signaling and inhibits budding, broken yellow line) and Bmp4 in the distal epithelium. Bmp4 possibly also inhibits distal budding through autocrine signaling from the epithelium (Eblaghie et al., 2006) (broken yellow line) and can also enhance budding in a paracrine fashion (broken yellow arrow), via an unidentified mesenchymal signal (X). Mesenchymal Pod1 (Tcf21) (indirectly) and epithelial Wnt signaling regulate Bmp4 (see F). Mechanisms that might inhibit ectopic budding in stalk regions include: netrin-mediated Fgfr2b signaling inhibition (broken yellow line); Tgfb activation in the epithelium by Tgfb1 from the subepithelial mesenchyme; Tgfb1-induced synthesis of extracellular matrix (ECM) components,such as collagen and fibronectin, and Tgfbi in stalk mesenchyme. (C)Control of Fgf10 and Fgfr2b expression. Canonical Wnt signaling activates Fgfr2b expression in the lung epithelium;mesenchymal Wnt (alone or with epithelial Wnt) inhibits Fgf10. Positive regulators of Fgf10 include Foxf1, Tbx4 and Tbx5. Tgfb1 signaling in stalk mesenchyme may prevent Fgf10 expression in the proximal mesenchyme (box in C). Shh signaling in the distal mesenchyme inhibits Fgf10 expression, but via Gli3 also controls availability of Foxf1, a positive regulator of Fgf10. Shh induction of Hhipexpression inhibits Shh signaling (broken yellow line) to allow Fgf10expression. (D) At the bud tips, high Shh (distal epithelium) and Hhip(distal mesenchyme) levels result in overall less Shh signaling and more Fgf10 than in the immediately adjacent regions, where Shh signaling is unopposed by Hhip. Low Shh levels in more proximal bud regions allow Fgf10 expression in the adjacent mesenchyme, resulting in later induction of lateral buds. (E) The proliferation of multipotent mesenchymal progenitors while the lung grows depends on Shh and Wnt7b signals from the distal epithelium and on Fgf9 from the pleura (purple). Foxa1 and Foxa2 regulate Shh and Wnt7b expression. Vegf regulates endothelial cell differentiation. RA (from the pleura) may regulate Fgf9 expression but this remains to be shown. (F) A model of proximodistal cell fate regulation in the lung bud epithelium. Mycn and Fgf10(via Fgfr2b epithelial signaling) maintain the proliferation of progenitor cells of the distal lung epithelium. Bmp4 prevents distal epithelial cells from assuming a proximal phenotype. Wnt signaling regulates the timing of their differentiation (presumably by controlling Bmp4 and Mycn expression) and is negatively regulated by dickkopf 1 (Dkk1). Foxj1 induces differentiation of proximal epithelium into ciliated cells. See text for references and Eblaghie et al.(Eblaghie et al., 2006).

Fig. 3.

Models of bud formation and proximodistal patterning in the developing lung. A developing lung bud during branching morphogenesis. Mesenchyme is depicted in gray and the epithelium in blue or red (distal bud). (A)Branching initiates with local Fgf10 expression in the distal mesenchyme. Fgf10 diffuses (yellow arrow) and binds locally to Fgfr2b(expressed throughout the lung epithelium) to activate signaling and induce a bud (white arrow). (B) As the bud elongates, Fgfr2b signaling induces expression of Spry2 (which negatively regulates Fgf signaling and inhibits budding, broken yellow line) and Bmp4 in the distal epithelium. Bmp4 possibly also inhibits distal budding through autocrine signaling from the epithelium (Eblaghie et al., 2006) (broken yellow line) and can also enhance budding in a paracrine fashion (broken yellow arrow), via an unidentified mesenchymal signal (X). Mesenchymal Pod1 (Tcf21) (indirectly) and epithelial Wnt signaling regulate Bmp4 (see F). Mechanisms that might inhibit ectopic budding in stalk regions include: netrin-mediated Fgfr2b signaling inhibition (broken yellow line); Tgfb activation in the epithelium by Tgfb1 from the subepithelial mesenchyme; Tgfb1-induced synthesis of extracellular matrix (ECM) components,such as collagen and fibronectin, and Tgfbi in stalk mesenchyme. (C)Control of Fgf10 and Fgfr2b expression. Canonical Wnt signaling activates Fgfr2b expression in the lung epithelium;mesenchymal Wnt (alone or with epithelial Wnt) inhibits Fgf10. Positive regulators of Fgf10 include Foxf1, Tbx4 and Tbx5. Tgfb1 signaling in stalk mesenchyme may prevent Fgf10 expression in the proximal mesenchyme (box in C). Shh signaling in the distal mesenchyme inhibits Fgf10 expression, but via Gli3 also controls availability of Foxf1, a positive regulator of Fgf10. Shh induction of Hhipexpression inhibits Shh signaling (broken yellow line) to allow Fgf10expression. (D) At the bud tips, high Shh (distal epithelium) and Hhip(distal mesenchyme) levels result in overall less Shh signaling and more Fgf10 than in the immediately adjacent regions, where Shh signaling is unopposed by Hhip. Low Shh levels in more proximal bud regions allow Fgf10 expression in the adjacent mesenchyme, resulting in later induction of lateral buds. (E) The proliferation of multipotent mesenchymal progenitors while the lung grows depends on Shh and Wnt7b signals from the distal epithelium and on Fgf9 from the pleura (purple). Foxa1 and Foxa2 regulate Shh and Wnt7b expression. Vegf regulates endothelial cell differentiation. RA (from the pleura) may regulate Fgf9 expression but this remains to be shown. (F) A model of proximodistal cell fate regulation in the lung bud epithelium. Mycn and Fgf10(via Fgfr2b epithelial signaling) maintain the proliferation of progenitor cells of the distal lung epithelium. Bmp4 prevents distal epithelial cells from assuming a proximal phenotype. Wnt signaling regulates the timing of their differentiation (presumably by controlling Bmp4 and Mycn expression) and is negatively regulated by dickkopf 1 (Dkk1). Foxj1 induces differentiation of proximal epithelium into ciliated cells. See text for references and Eblaghie et al.(Eblaghie et al., 2006).

Bud formation can be also controlled by diffusible signals originating from epithelial cells at the tips of nascent buds, which may alter levels or distribution of Fgf10 in the mesenchyme, and ultimately influence Fgf signaling in the epithelium. Shh is highly expressed in the distal epithelium,from where it diffuses to activate signaling in the corresponding mesenchyme via patched (Ptch1)/smoothened (Smo) and their transcriptional effectors Gli1,Gli2 and Gli3 (Bellusci et al.,1997a). Data from lung organ culture and in vivo studies support the idea that Shh negatively regulates Fgf10 expression in the lung(Bellusci et al., 1997a; Lebeche et al., 1999). These findings have led to the proposal that Shh at the bud tips progressively downregulates Fgf10 expression as a bud grows towards the Fgf10-expressing mesenchyme, thus limiting further bud outgrowth. By doing so, Shh would contribute to controlling bud size. Interestingly, Shh may also control the shape of the bud by preventing the widespread expression of Fgf10 in the mesenchyme and the generalized activation of Fgfr2b in the distal epithelium. In lungs from Shh-null mice, Fgf10transcripts are found diffusely expressed in the lung mesenchyme. Instead of forming typical buds, the epithelium develops as large cystic structures and branching morphogenesis is severely disrupted(Pepicelli et al., 1998). Precisely how Shh helps to control the spatial pattern of Fgf10expression is unknown. One potential way involves Shh induction of the hedgehog interacting protein Hhip1 in the distal mesenchyme. Hhip1 inhibits Shh signaling by ligand sequestration and, thus, releases Shh-mediated repression of Fgf10 locally (see Fig. 3D). In the lungs of Hhip1-null mice, branching is inhibited because of increased Shh activity and the nearly complete repression of Fgf10 expression in the developing lung (Chuang et al.,2003).

Bmp and Wnt signaling: positive or negative regulators of branching?

There have been apparently conflicting reports about how Bmp and Wnt signaling influence lung branching morphogenesis. Among the Bmp ligands present in the embryonic lung, Bmp4 is the best studied. Bmp4 is transcribed in the lung mesenchyme from its earliest stages, but it is not present in the epithelium until branching initiates. A Bmp4lacZ reporter mouse reveals a striking distribution of Bmp4 in the ventral foregut mesoderm at the prospective lung region as early as E9 (Weaver et al.,1999). The biological significance of this finding remains to be determined. By E11-12, Bmp4 transcripts are found in the distal lung epithelium and in the proximal mesenchyme(Weaver et al., 1999; Weaver et al., 2003). The Bmp4 receptor (type I, or Alk3), and the Bmp transducing Smad1 protein are present both in the epithelium and mesenchyme of the embryonic lung(Bellusci et al., 1996; Chen et al., 2005). A detailed analysis of Bmpr2 distribution in the early embryonic lung is not currently available. The patterns above suggest that Bmp4 signaling can be activated both in an autocrine fashion (in the epithelium) and in a paracrine fashion(in the mesenchyme).

The precise role of Bmp4 in the developing lung in vivo remains unclear, in part because of the early embryonic death of Bmp4-null mice(Winnier et al., 1995). It has been previously proposed that, during branching, Bmp4 is induced and activated in the epithelium of distal buds to limit Fgf10-mediated bud outgrowth. This model is supported by the following observations(Lebeche et al., 1999; Weaver et al., 2000). Analyses of E11.5 lungs undergoing branching morphogenesis show that Bmp4 expression in the lung epithelium is highest in distal buds,near Fgf10-expressing cells. Bmp4 is not induced in the epithelium of E11.5 lungs during bud initiation but appears later, once the bud is elongating. In mesenchyme-free lung epithelial cultures, recombinant Fgf10 induces budding and Bmp4 expression, while recombinant Bmp4 inhibits the Fgf10-mediated budding in these cultures.

Paradoxically, when recombinant Bmp4 is administered to intact lung explants in which the epithelium and mesenchyme are present, branching is enhanced (Bragg et al., 2001). An alternative model has been proposed to explain how Bmp4 can have both positive and negative effects in the lung. The model predicts that the mesenchyme influences the ability of the epithelium to respond to Bmp4. When Bmp4 signaling is activated in the epithelium in an autocrine fashion,proliferation is inhibited (but see Eblaghie et al., 2006). In the intact lung, however, Bmp4 present in the distal epithelium may also activate Bmp signaling in the adjacent mesenchyme (paracrine fashion). Bmp4, then,induces a currently unidentified distal mesenchymal signal that enhances proliferation of distal epithelial buds(Bragg et al., 2001). In this way, negative or positive effects on branching would depend on whether Bmp signaling is activated via an autocrine or a paracrine mechanism(Fig. 3B). Regulation of Bmp4 in the epithelium is complex and dependent on signals such as Wnt (see below), Fgf10 and Pod1 (Tcf21), a transcriptional factor present in the mesenchyme (Quaggin et al.,1999).

The role of Wnt signaling in lung branching morphogenesis has also been debated. Several Wnt ligands, frizzled receptors and components of the Wnt canonical pathway, such as β-catenin, and Tcf/Lef transcription factors(see http://www.stanford.edu/~rnusse/wntwindow.html)are present in the developing lung(Bellusci et al., 1996; Lako et al., 1998; Zakin et al., 1998; Tebar et al., 2001). Activation of canonical Wnt signaling can be monitored by detection of nuclear translocated β-catenin, and by analysis of a Wnt responsive reporter mouse (TOPGAL), in which lacZ is expressed where theβ-catenin-Lef1/Tcf complex activates the transcription of Wnt targets(Nelson and Nusse, 2004; DasGupta and Fuchs, 1999). In the E11-13 lung, β-catenin is expressed throughout the entire lung epithelium. However, nuclear-localized β-catenin, Tcf/Lef transcripts and lacZ-TOPGAL expression are increased in the distal lung epithelium,the sites that are actively branching(Okubo and Hogan, 2004; De Langhe et al., 2005). Disruption of canonical Wnt signaling at these sites by targeted deletion ofβ-catenin, or by targeted expression of the Wnt inhibitor dickkopf 1 in vivo, prevents distal lung buds from forming and markedly interferes with branching morphogenesis. The defect appears to result, at least in part, from failure to induce proper levels of Fgfr2b in the distal lung epithelium where Wnt/β-catenin signaling is inhibited(Mucenski et al., 2003; Shu et al., 2005). It has been pointed out, however, that although β-catenin deletion is a good method for disrupting all Wnt canonical signaling, other β-catenin functions, not necessarily related to Wnt signaling, may be also affected(Dean et al., 2005). Indeed,β-catenin is also found in cell membranes in a cadherin-bound form that regulates cell adhesion. Thus, it is possible that the branching defect reported in the models in which β-catenin was deleted from the epithelium could have resulted from changes to both its Wnt and non-Wnt functions(Dean et al., 2005).

Interestingly, the results above conflict with that of two other models that show increased branching morphogenesis as a consequence of disrupted Wnt signaling. In one model, lung explants were treated with morpholino oligonucleotides against β-catenin; the other is a genetic model in which mice lack the Wnt5a gene (a non-canonical Wnt, normally present in the lung epithelium and mesenchyme) (Li et al., 2002; Dean et al.,2005). In both cases, Fgf10 expression was locally increased in these lungs. It is possible that this discrepancy in results is due to the fact that in the morpholino and Wnt5a models, Wnt signaling was inactivated in both the epithelium and mesenchyme. In addition,canonical and non-canonical Wnts (and even different Wnt family members) may have distinct functions (Fig. 3C,E,F). Further studies are required to clarify these issues.

The discussion in this section underscores the complexity of the Bmp4 and Wnt signaling during branching, and the importance of taking into account the overall balance of these signals in the epithelium and mesenchyme. In addition, both Bmp4 and canonical Wnt are required for the establishment of distal epithelial cell fate in the lung (see below).

Tgfb signaling as a negative regulator of branching morphogenesis

Tgfb1, Tgfb2 and Tgfb3, members of the Tgfb subfamily, have also been implicated in the control of lung branching morphogenesis. These Tgfb ligands,their receptors (Tgfbr1 and Tgfbr2) and transducing proteins Smad2 and Smad3,are expressed in the developing mouse lung. Many of the biological activities of these Tgfb proteins differ only in the intensity of their effects (reviewed by Massague, 2000). During lung branching morphogenesis, Tgfb1 is transcribed in the mesenchyme adjacent to the epithelium, without an obvious proximodistal gradient(Lebeche et al., 1999). However Tgfb1 protein accumulates in stalks and in regions in between buds,where extracellular matrix components collagen I, collagen III and fibronectin are also present (Heine et al.,1990). Tgfb2 is expressed in the distal lung epithelium,while Tgfb3 is present in the proximal lung epithelium, mesenchyme and pleura (Pelton et al.,1991). Analysis of Tgfb2- or Tgfb3-null mice reveals that lung branching morphogenesis is affected by the lack of Tgfb3, but not by Tgfb2 deficiency(Sanford et al., 1997; Kaartinen et al., 1995).

Exogenous Tgfb1 inhibits branching morphogenesis, growth and differentiation in cultured mouse embryonic lungs(Serra et al., 1994; Zhao et al., 1996). This effect has been also reported in transgenic mice misexpressing Tgfb1in the distal epithelium (Zhou et al.,1996). Interestingly, Tgfb1-null mice show no obvious structural lung defect and die perinatally of a diffuse inflammatory syndrome(Letterio et al., 1994). Whether Tgfb1 is dispensable for lung morphogenesis has been debated, as there is evidence that the phenotype may have been rescued by maternal transfer of Tgfb1. Studies in NIH3T3 fibroblasts, lung and prostate organ cultures indicate that activation of Tgfb1 signaling in mesenchymal cells markedly inhibits Fgf10 expression (Beer et al., 1997; Lebeche et al.,1999; Tomlinson et al.,2004). In the developing lung, Tgfb1 may be part of a mechanism that prevents Fgf10 from being expressed in the mesenchyme of bud stalks or in more proximal regions of the lung. At these sites, Tgfb1 could also induce synthesis of extracellular matrix components and prevent budding locally (Fig. 3B).

Refining patterning and preventing ectopic budding

Branching patterns can be further refined by mechanisms that regulate bud formation at specific locations in the developing lung. For example, the transcription factor Foxf1 is expressed throughout the mesenchyme of both lungs from the earliest developmental stages. However, analysis of Foxf1 heterozygous mice at E10-11 suggests that Foxf1 is required for proper gene expression and budding selectively in the cranial, middle and accessory lobes of the right lung. These mice show low levels of Fgf10 and Gli3 mRNAs, and display altered lung bud orientation and ectopic budding in these lobes, among other abnormalities(Lim et al., 2002; Mahlapuu et al., 2001). The presence of lung defects that resemble those from Gli3-null mutants suggest a genetic interaction between Foxf1 and Shh signaling via Gli3 (Fig. 3C). Foxf1expression is in part regulated by Shh signaling through Shh-dependent processing of Gli3 (Li et al.,2004).

Other genes are dynamically expressed at the stalks of branching tubules in a pattern that suggests a role in preventing local budding(Fig. 3B). This is the case of the axon guidance molecules netrin 1 and netrin 4, and the extracellular matrix protein Tgfb induced (Tgfbi or βig-h3) in the E11-13 mouse lung. There is evidence that netrins and their receptors Unc5b and Dcc (deleted in colorectal cancer) are present in the lung epithelium at these stages. Moreover, exogenous netrin inhibits Fgf-mediated Erk phosphorylation and bud formation in mesenchyme-free lung epithelial explants(Liu et al., 2004). These observations favor the hypothesis that, during branching morphogenesis, netrin expression in stalks prevents buds from forming in these region by interfering with local activation of Fgf signaling(Liu et al., 2004). This hypothesis, however, has not been confirmed in vivo, as genetic inactivation of netrins or other axon guidance molecules, such as semaphorins (or Slit and Robo proteins) in mice has not resulted in obvious defects in lung branching morphogenesis (Hinck, 2004). Recent evidence demonstrating that Slit2 and netrin 1 act synergistically in mammary gland ductal morphogenesis suggests that deciphering the role of axon guidance molecules in the lung will require simultaneous inactivation of more than one member of these functionally related families of genes(Strickland et al.,2006).

Tgfbi, another molecule dynamically expressed in stalks and in interbud regions of the developing lung, is present in the mesenchyme, at sites traditionally associated with Tgfb-induced deposition of extracellular matrix and decreased epithelial cell proliferation(Serra et al., 1994; Zhao et al., 1996; Heine et al., 1990; Lu et al., 2004). Tgfbi is known to be induced by Tgfb1 and to mediate Tgfb responses in some cell systems by a mechanism that is still unclear(Kim et al., 2003). Tgfbi binds to a variety of matrix molecules, such as fibronectin and collagen(Billings et al., 2002). Whether Tgfbi restricts bud formation in stalks during lung branching morphogenesis is currently unknown.

What is downstream of Fgf signaling during lung bud formation?

There is still little understanding of the cellular mechanisms of lung bud formation and of the targets of Fgf10 in this process. In Drosophila,Fgf signaling activation causes dynamic actin-based filopodial extensions at the tip of primary branches, leading to epithelial migration. This is in part promoted by the induction of pointed (Spdef - Mouse Genome Informatics) an Ets transcription factor(Samakovlis et al., 1996; Sutherland et al., 1996). In the E11.5 mouse lung, two Ets family members, Pea3 and Erm (Etv4 and Etv5,respectively), have been identified in the distal epithelium. Although both are downstream of the Fgfr2b pathway, they do not seem to be required for branching, as shown by expression of a dominant-negative Erm targeted to the lung in vivo (Liu et al.,2003).

A microarray-based screen to identify Fgf10 targets in mesenchyme-free lung epithelial buds has shown that the initial stages of budding are characterized by upregulation of genes traditionally associated with: cell rearrangement and cell migration [Tm4sf3, transmembrane 4 superfamily member 3(Tspan8); the Notch signaling antagonist Numb; and Lmo7, LIM domain only 7]; inflammatory processes (annexins); lipid metabolism [HSL, hormone-sensitive lipase (Lipe)];proteolysis (cathepsin H, Timp3); and metastatic behavior(Tacstd2, tumor-associated calcium signal transducer 2), but not cell proliferation (Lu et al.,2005a). This

observation is consistent with previous studies that show local changes in proliferation are not the triggering event that initiates lung budding(Nogawa et al., 1998).

graphic

Box 1. Myogenesis and bud morphogenesis

Airway smooth muscle starts to form relatively early in the developing mouse lung. A smooth muscle layer adjacent to the epithelium of the trachea and primary lung buds is present at E11 and continues to form around proximal,but not distal, epithelial tubules as branching proceeds(Tollet et al., 2001). Interestingly, airway smooth muscle appears partly to originate from a pool of progenitor cells in the distal lung mesenchyme that undergoes a program of differentiation that initially depends on Shh and Bmp4, signals expressed mostly by distal epithelial buds. How can these distal signals influence differentiation of a proximal mesenchymal derivative? A model has been proposed to resolve this apparent paradox (see figure)(Mailleux et al., 2005; Weaver et al., 2003).(A) Initially, lung epithelial buds (blue) are induced by Fgf10 from the distal mesenchyme, which, in turn, is exposed to high Bmp4 (induced in the epithelium by Fgf10) and Shh levels that diffuse from the tips of growing buds(red region, A-C). (B) This triggers a myogenic program in distal mesenchymal cells that continues while they are relocated to more proximal regions by continued bud outgrowth (large white arrow, B) and/or by active mesenchymal cell migration (small white arrows, B). (C) The myogenic program completes once these progenitor cells are located along proximal airways. This model is supported by analysis of an Fgf10lacZ reporter mouse, which labels Fgf10-expressing distal mesenchymal cells and airway smooth muscle(Mailleux et al., 2005). Furthermore, a hypomorphic Fgf10 mouse mutant, in which low Fgf10 levels result in reduced Bmp4 expression and epithelial branching,showed decreased smooth muscle differentiation. Smooth muscle cell differentiation also depends on physical stretch, serum response factor,laminin 2, tension-induced proteins such as Tip1 and on Wnt signaling-mediated induction of fibronectin (Yang et al.,2000; De Langhe et al.,2005; Jakkaraju et al.,2005).

Patterning the mesenchyme

Integrating epithelial and pleural signals

Lung mesenchyme development is crucially influenced by signals from the epithelium and the pleura (Fig. 3E, Box 1, Table 1) that, in concert,appear to maintain a balance of differentiated and proliferating multipotent progenitors while the lung grows (Weaver et al., 2003). Epithelial buds are a source of trophic or differentiation signals for the mesenchyme, such as Shh, Vegf and Wnt7b, among others. Lungs from Shh-null mice show inhibited mesenchymal cell proliferation and smooth muscle differentiation, and severe hypoplasia, a condition characterized by abnormal small lungs(Pepicelli et al., 1998). Wnt7b-null mouse mutants also have defective vascular smooth muscle differentiation and are also severely hypoplastic(Shu et al., 2002). Vegf is crucial for several aspects of vascular development, and for epithelial-endothelial interactions during branching morphogenesis(Pauling and Vu, 2004; Del Moral et al., 2006).

The transcription factors Foxa1 and Foxa2 are present in the lung epithelium and have been shown to influence both epithelial and mesenchymal programs by regulating the levels of expression of Shhand Wnt7b. The conditional deletion of Foxa1 and Foxa2 in the distal lung epithelium of transgenic mice inhibits Shh and Wnt7b expression and results in disrupted branching morphogenesis and smooth muscle differentiation(Fig. 3E)(Wan et al., 2005). It has been proposed that the pleura controls proliferation and the differentiation status of the distal mesenchyme (Weaver et al., 2003). Indeed, mesothelial cells of the pleura express a number of signaling molecules such as Fgf9, Tgfb3 and RA, which can mediate these activities (Colvin et al.,2001; Bragg et al.,2001; Malpel et al.,2000). Mice in which these pathways have been inactivated have pulmonary hypoplasia. Fgf9 (also present in the distal epithelium), probably signaling via Fgfr1c, acts as a trophic factor for the distal mesenchyme. Fgf9 mutants have a markedly reduced number of mesenchymal cells,which results in less Fgf10 being available overall to induce normal epithelial branching (Colvin et al.,2001). Fgf9 prevents Shh-induced differentiation of the lung mesenchyme into smooth muscle in vitro(Weaver et al., 2003).

The RA synthesizing enzyme Raldh2(Niederreither et al., 1999)is co-expressed with Fgf9 in the pleura, and it is possible that Fgf9 expression is regulated by RA in mesothelial cells(Malpel et al., 2000; Colvin et al., 1999). In the developing heart, RA from mesothelial cells of the epicardium induces Fgf9, which then activates an Fgf pathway that is essential for cardiomyoblast expansion (Lavine et al.,2005). As in Fgf9-null mice, lung hypoplasia has been also associated with disruption of RA signaling(Wilson et al., 1953).

Generating cell diversity

Mechanisms influencing proximal-distal cell fate and epithelial differentiation

The mature respiratory epithelium consists of multiple cell types,including ciliated, neuroendocrine and secretory cells present in proximal regions of the respiratory system, and type I and type II cells that are typical of the distal alveolar region of the lung. Cell fate is established along the proximodistal axis of the respiratory epithelium as lung buds form and branch, and seems to depend on a distal signaling center in which Bmp4 and Wnt canonical signaling are crucial. When Bmp signaling is inhibited in transgenic mice by targeting a dominant-negative Bmp receptor(dnAlk6) or Bmp antagonists (noggin, gremlin) to the distal lung epithelium, development of the distal epithelium is severely impaired and the lung becomes `proximalized' (Weaver et al., 1999; Lu et al.,2001). In the model proposed by the authors of these studies,disrupted Bmp signaling makes lung epithelial cells from distal buds acquire a proximal phenotype and stop branching. Proximalization also results from the targeted deletion of β-catenin in the distal lung epithelium(Weaver et al., 1999; Mucenski et al., 2003; Lu et al., 2001). Thus, a gradient of Bmp4 and Wnt signaling, with the highest levels of activation in distal epithelial buds, is thought to prevent distal cells from assuming a proximal phenotype (Fig. 3F). At subsequent stages, other molecules contribute to the differentiation of the epithelium into specific cell types. For example, in the proximal lung, the forkhead box transcription factor Foxj1 is required to form ciliated cells (Chen et al., 1998).

Disrupted distal lung development is also seen in transgenic mice in which RA signaling is constitutively activated in the distal lung epithelium throughout branching morphogenesis(Wongtrakool et al., 2003). Endogenous RA signaling is active during primary lung bud formation, but is downregulated in the epithelium once secondary budding and branching initiates(Malpel et al., 2000). Interestingly, in the transgenic model above, RA signaling persists in the distal epithelium, as during early developmental stages. As a result, distal lung progenitors are present but do not undergo further differentiation and remain immature (Wongtrakool et al.,2003). Thus, in the developing lung, RA seems to act as a developmental switch. RA is initially `on' to activate an early developmental program, but later it has to be turned `off' to allow subsequent stages of this program to take place in the distal lung.

Maintaining progenitor cells while differentiating

As epithelial cells in branching airways continue to differentiate, it is crucial to maintain and expand a pool of uncommitted progenitor cells for continued growth. It has been proposed that this pool resides in the distal lung, as a population of proliferating immature epithelial cells that expresses high levels of the proto-oncogene Mycn. Targeted disruption of Mycn expression in distal lung epithelial cells of mutant mice inhibits distal lung proliferation and induces premature differentiation(Okubo et al., 2005). Inhibition of Wnt canonical signaling in mutant mice causes a similar lung phenotype and shows that Wnt controls levels of Mycn and Bmp4 expression in the distal lung(Shu et al., 2005)(Fig. 3F). There is also evidence that activation of Fgf10 and Fgfr2b signaling in the developing pancreas, tooth, skin and the lung may be required to expand or maintain a pool of epithelial progenitor cells during organogenesis(Harada et al., 2002; Bhushan et al., 2001; Norgaard et al., 2003).

Cell plasticity: reprogramming cell fates

There is accumulated evidence in vitro and in vivo that developmental programs can be altered in cells that have initially embarked on a specific lineage pathway, simply by changing the type or amount of signals in the local environment. This has been documented in tissue recombination experiments in vitro. Reprogramming of tracheal epithelium or ureteric bud by lung mesenchyme has been demonstrated by the induction of a lung-specific pattern of branching and differentiation that is not normally present in tracheal or ureteric progenitor cells (Lin et al.,2003; Shannon,1994). These observations are consistent with the idea that local inductive signals from the mesenchyme confer novel position-specific information that radically changes epithelial cell fate. Fgf proteins,collagen XVIII, Wnt2, Shh and transferrin are some of the molecules that have been implicated in the in vitro reprogramming of the lung epithelium(Lin et al., 2003; Hyatt et al., 2004; Ohtsuka et al., 2001). Lung epithelial reprogramming has also been shown in vivo in transgenic mice harboring a Sfptc-driven constitutively active β-catenin/Lef fusion protein construct (Okubo and Hogan, 2004). Remarkably, these lungs lack differentiated lung cell types and show a hyperproliferative epithelium that expresses Cdx1,Atoh1 and other genes involved in the establishment of intestinal cell lineages. Although it is not clear exactly when the transgene starts to act,the successful targeting of the transgene to Sftpc-expressing cells suggests that increased Wnt signaling leads lung progenitor cells to change their fate into an intestinal secretory cell fate. Whether Wnt signaling influences the initial specification of the lung field in the primitive foregut, remains to be investigated.

Conclusion

Overall, the studies so far suggest that the major events in early lung morphogenesis are controlled by a relatively limited group of molecules (Fgfs,Tgfb, Shh, Wnt proteins). Novel insights will be gained by exploring the different ways by which expression or activation of these molecules is controlled; these include gene methylation, endogenous microRNAs and proteolysis, among other mechanisms (Lu et al., 2005b; Harris et al.,2006; Li et al.,2004). A crucial role for heparan and chondroitin sulfate proteoglycans as modulators of growth factor distribution and signaling in organogenesis has been well documented in several developing systems. In Drosophila, integrity and proper sulfation of heparan are essential for Fgf signaling and tracheal morphogenesis(Kamimura et al., 2001). There is evidence that this is also true for the mammalian lung, but the mechanisms remain to be understood (Izvolsky et al.,2003; Shannon et al.,2003).

The lack of early markers of lung progenitor cells represents a clear gap of knowledge in the field. Because Sftpc expression cannot be identified prior to the emergence of primary buds, Nkx2.1 is the only early marker currently available for these cells. A confounding issue is that this gene is also expressed by the thyroid. Laser capture microdissection approaches and detailed gene profiling analysis of the developing foregut will be useful to find other markers of lung progenitor cells. Also crucial will be the development of tools for targeting genes to these early progenitors in the foregut in future functional studies.

Still relatively little is known about the changes that are induced in the milieu around the nascent lung bud and in the bud itself when Fgf10 activates Fgfr2b. How do cells rearrange to form new buds? These questions require powerful image analysis systems and an array of markers, which may be already available.

A rather more complex problem is the understanding of how the coordinates that set up the three-dimensional pattern of morphogens, such as Fgf10, are established in the lung. Finally, there is the much debated issue of stem cells. What are these cells? Where are their niches in the developing lung?How can they be identified? Tackling these issues will provide insights into the molecular and cellular mechanisms by which the lung develops.

Note added in proof

A recent report by Eblaghie et al.(Eblaghie et al., 2006)provides genetic evidence that Bmpr1a mediates an autocrine signaling required for distal lung epithelial cell proliferation and survival.

Acknowledgements

We thank Mark Krasnow, Jerry Brody and Mary Williams for helpful discussions. We also thank present and former members of the laboratory(Felicia Chen, Konstantin Izvolsky, Jeff Sedita, Tushar Desai, Cherry Wongtrakool and Sarah Malpel) for valuable insights and for some of the work cited here. We are grateful to Brigid Hogan for critical reading of the manuscript. The authors research is, in part, supported by NIH/NHLBI.

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