The majority of the skeleton arises by endochondral ossification, whereby cartilaginous templates expand and are resorbed by osteoclasts then replaced by osteoblastic bone formation. Ephrin B2 is a receptor tyrosine kinase expressed by osteoblasts and growth plate chondrocytes that promotes osteoblast differentiation and inhibits osteoclast formation. We investigated the role of ephrin B2 in endochondral ossification using Osx1Cre-targeted gene deletion. Neonatal Osx1Cre.Efnb2Δ/Δ mice exhibited a transient osteopetrosis demonstrated by increased trabecular bone volume with a high content of growth plate cartilage remnants and increased cortical thickness, but normal osteoclast numbers within the primary spongiosa. Osteoclasts at the growth plate had an abnormal morphology and expressed low levels of tartrate-resistant acid phosphatase; this was not observed in more mature bone. Electron microscopy revealed a lack of sealing zones and poor attachment of Osx1Cre.Efnb2Δ/Δ osteoclasts to growth plate cartilage. Osteoblasts at the growth plate were also poorly attached and impaired in their ability to deposit osteoid. By 6 months of age, trabecular bone mass, osteoclast morphology and osteoid deposition by Osx1Cre.Efnb2Δ/Δ osteoblasts were normal. Cultured chondrocytes from Osx1Cre.Efnb2Δ/Δ neonates showed impaired support of osteoclastogenesis but no significant change in Rankl (Tnfsf11) levels, whereas Adamts4 levels were significantly reduced. A population of ADAMTS4+ early hypertrophic chondrocytes seen in controls was absent from Osx1Cre.Efnb2Δ/Δ neonates. This suggests that Osx1Cre-expressing cells, including hypertrophic chondrocytes, are dependent on ephrin B2 for their production of cartilage-degrading enzymes, including ADAMTS4, and this might be required for attachment of osteoclasts and osteoblasts to the cartilage surface during endochondral ossification.

Endochondral ossification is the process by which the majority of the skeleton develops. In this process, the cartilage model enlarges by chondrocyte proliferation, until it reaches a size where the central chondrocytes undergo hypertrophy. Two processes then take place: the periosteal bone collar is deposited by osteoblasts around the diaphysis (mid-shaft), and cartilage and hypertrophic chondrocytes are gradually destroyed by osteoclasts (bone-resorbing cells). The resulting cartilage remnants are gradually replaced with bone by repeated cycles of resorption by osteoclasts followed by osteoblastic bone formation; this process continues throughout skeletal growth. It has been suggested that mechanisms controlling osteoclast generation and activity at the growth plate may be distinct from those that exist on bone surfaces during adulthood (Poulton et al., 2012; Touaitahuata et al., 2014), but these remain poorly defined.

Ephrin B2 is a tyrosine kinase that is expressed in the skeleton in osteoblasts (bone-forming cells), matrix-embedded osteocytes and osteoclasts (Zhao et al., 2006; Allan et al., 2008). Its expression by osteoblasts is rapidly upregulated by parathyroid hormone (PTH) and the related protein (PTHrP; also known as PTHLH) (Allan et al., 2008). The interaction of ephrin B2 with Eph receptor B4 (EPHB4) restricts the ability of bone surface osteoblasts to support osteoclast formation (Takyar et al., 2013). This interaction also promotes osteoblast differentiation (Takyar et al., 2013) and prevents their apoptosis (Tonna et al., 2014). This is required for bone to be mineralised at the normal rate, thereby contributing to bone strength (Tonna et al., 2014) and, at least in part, mediating the anabolic effect of pharmacological PTH (Takyar et al., 2013; Tonna and Sims, 2014; Tonna et al., 2014).

Osteoblasts and chondrocytes are derived from a common precursor pool, and although it was originally thought that they are separate lineages, more recent studies indicate plasticity and transdifferentiation between these two cell types (Yang et al., 2014a,,b; Zhou et al., 2014; Park et al., 2015). Both ephrin B2 and EPHB4 are detected in proliferating and hypertrophic chondrocytes at the growth plate (Wang et al., 2014), during fracture healing (Ito et al., 2006), in articular cartilage (Othman-Hassan et al., 2001), and in the ATDC5 chondrocyte cell line (Ito et al., 2006; Wang et al., 2014). At the growth plate, ephrin B2 and EPHB4 protein levels are reported to be lower in the absence of IGF1 (Wang et al., 2014), a factor that promotes chondrocyte proliferation during longitudinal bone growth downstream of growth hormone (Sims et al., 2000). Although pharmacological inhibition of ephrin B2/EPHB4 signalling in osteoblasts promoted RANKL (also known as TNFSF11) production and support of osteoclast formation (Takyar et al., 2013), the same reagent suppressed osteoclast formation when supported by chondrocytes (Wang et al., 2014). This latter effect appeared to be independent of RANKL production (Wang et al., 2014). This suggested that ephrin B2 regulates osteoclast formation by restraining the expression of RANKL in osteoblasts but promoting a RANKL-independent action that supports osteoclastogenesis in chondrocytes.

In this study, we targeted the deletion of ephrin B2 (Efnb2) to chondrocytes and osteoblasts in a mouse model (Osx1Cre.Efnb2Δ/Δ), and found that these mice exhibit a neonatal osteopetrosis due to impaired osteoclastogenesis specifically at the growth plate. This points to a novel role for ephrin B2 in the chondrocyte that is required for osteoclastogenesis and cartilage destruction during endochondral ossification.

Increased trabecular bone volume due to impaired osteoclast activity

von Kossa staining revealed substantially higher trabecular bone mass, including the presence of intact chondrocyte stacks (green boxes, Fig. 1A), in 2-day-old Osx1Cre.Efnb2Δ/Δ mice as compared with controls comprising wild-type mice (Efnb2w/w), mice harbouring Osx1Cre but lacking the Efnb2-loxP transgene (Osx1Cre.Efnb2w/w), and mice expressing two copies of the Efnb2-loxP transgene (Efnb2f/f). Histomorphometric analysis (Fig. 1B) confirmed a significantly higher trabecular bone volume (BV/TV) and trabecular number (Tb.N) in Osx1Cre.Efnb2Δ/Δ femora compared with littermate controls, consistent with osteopetrosis (Fig. 1B). Trabecular thickness (Tb.Th) and trabecular separation were both significantly less than in controls. No significant effect of the Osx1Cre transgene on trabecular bone structure was detected. Similar observations were made in distal tibiae, proximal femur and distal femur (data not shown).

Fig. 1.

Increased trabecular bone mass in neonatal Osx1Cre.Efnb2Δ/Δ mice. (A) von Kossa-stained images of the distal tibiae of 3.5-day-old Osx1Cre.Efnb2Δ/Δ mice (far right), littermate Efnb2f/f controls, and age-matched wild-type (Efnb2w/w) and Osx1Cre.Efnb2w/w littermate controls. Green boxes indicate remnant chondrocyte stacks; the white box indicates the region used for histomorphometry. Scale bars: 50 μm. (B) Histomorphometry of the distal tibiae. Trabecular bone volume (BV/TV), trabecular number (Tb.N), trabecular thickness (Tb.Th) and trabecular separation (Tb.Sp) were assessed in Osx1Cre.Efnb2Δ/Δ mice (far right bar), littermate Efnb2f/f controls, and age-matched Efnb2w/w and littermate Osx1Cre.Efnb2w/w mice at 2.5-3.5 days of age. Data are expressed as a percentage of values obtained in Cre-negative littermates calculated within each litter to account for slight differences in age; error bars indicate s.e.m. *P<0.05, **P<0.01, ***P<0.001 versus all controls. n=5 Efnb2w/w, n=9 Osx1Cre.Efnb2w/w, n=5 Efnb2f/f and n=6 Osx1Cre.Efnb2f/f.

Fig. 1.

Increased trabecular bone mass in neonatal Osx1Cre.Efnb2Δ/Δ mice. (A) von Kossa-stained images of the distal tibiae of 3.5-day-old Osx1Cre.Efnb2Δ/Δ mice (far right), littermate Efnb2f/f controls, and age-matched wild-type (Efnb2w/w) and Osx1Cre.Efnb2w/w littermate controls. Green boxes indicate remnant chondrocyte stacks; the white box indicates the region used for histomorphometry. Scale bars: 50 μm. (B) Histomorphometry of the distal tibiae. Trabecular bone volume (BV/TV), trabecular number (Tb.N), trabecular thickness (Tb.Th) and trabecular separation (Tb.Sp) were assessed in Osx1Cre.Efnb2Δ/Δ mice (far right bar), littermate Efnb2f/f controls, and age-matched Efnb2w/w and littermate Osx1Cre.Efnb2w/w mice at 2.5-3.5 days of age. Data are expressed as a percentage of values obtained in Cre-negative littermates calculated within each litter to account for slight differences in age; error bars indicate s.e.m. *P<0.05, **P<0.01, ***P<0.001 versus all controls. n=5 Efnb2w/w, n=9 Osx1Cre.Efnb2w/w, n=5 Efnb2f/f and n=6 Osx1Cre.Efnb2f/f.

Osteopetrosis in Osx1Cre.Efnb2Δ/Δ neonatal mice was further indicated by Safranin O staining, which showed excessive cartilage remnants within the neonatal femoral diaphysis compared with Efnb2f/f littermates (Fig. 2A). There was also very little osteoid matrix on cartilage surfaces near the growth plate in Osx1Cre.Efnb2Δ/Δ (Fig. 2A). This is consistent with their low trabecular thickness, and suggests impaired osteoblast function. Although cartilage remnants within the trabecular bone were more abundant, the width of the hypertrophic zone was not significantly greater in neonatal Osx1Cre.Efnb2Δ/Δ mice compared with controls [mean hypertrophic zone width (μm)±s.e.m.: Osx1Cre.Efnb2w/w, 120±8 (n=8); Osx1Cre.Efnb2Δ/Δ, 156±20 (n=6); P=0.089].

Fig. 2.

Accumulation of cartilage remnants, lack of osteoid, and defective osteoclast formation at the chondro-osseous junction in Osx1Cre.Efnb2Δ/Δ mice. (A) Safranin O/Fast Green staining of femora from 3.5-day-old Osx1Cre.Efnb2Δ/Δ and Efnb2f/f littermates showing metaphyseal cartilage remnants (orange; extent marked with dashed line on the left) in Osx1Cre.Efnb2Δ/Δ femora. Boxes indicate approximate regions shown at high magnification on the right. Arrows indicate osteoid deposition (turquoise) on cartilage within the primary spongiosa in Efnb2f/f but a lack of osteoid in Osx1Cre.Efnb2Δ/Δ samples. (B) TRAP staining of 3.5-day-old Osx1Cre.Efnb2Δ/Δ and Efnb2f/f littermates indicates altered osteoclast morphology at the growth plate in Osx1Cre.Efnb2Δ/Δ samples. co, chondro-osseous junction; m, metaphysis; d, diaphysis. (C) Quantification of large (>15 μm2) and small (<15 μm2) TRAP-positive osteoclasts at the growth plate chondro-osseous junction and in the diaphysis of Osx1Cre.Efnb2Δ/Δ and Efnb2f/f littermates at 2.5-3.5 days of age. *P<0.05 versus Efnb2f/f (large), **P<0.01 versus Efnb2f/f (small). n=6 Efnb2w/w and n=7 Osx1Cre.Efnb2f/f. Scale bars: 50 μm.

Fig. 2.

Accumulation of cartilage remnants, lack of osteoid, and defective osteoclast formation at the chondro-osseous junction in Osx1Cre.Efnb2Δ/Δ mice. (A) Safranin O/Fast Green staining of femora from 3.5-day-old Osx1Cre.Efnb2Δ/Δ and Efnb2f/f littermates showing metaphyseal cartilage remnants (orange; extent marked with dashed line on the left) in Osx1Cre.Efnb2Δ/Δ femora. Boxes indicate approximate regions shown at high magnification on the right. Arrows indicate osteoid deposition (turquoise) on cartilage within the primary spongiosa in Efnb2f/f but a lack of osteoid in Osx1Cre.Efnb2Δ/Δ samples. (B) TRAP staining of 3.5-day-old Osx1Cre.Efnb2Δ/Δ and Efnb2f/f littermates indicates altered osteoclast morphology at the growth plate in Osx1Cre.Efnb2Δ/Δ samples. co, chondro-osseous junction; m, metaphysis; d, diaphysis. (C) Quantification of large (>15 μm2) and small (<15 μm2) TRAP-positive osteoclasts at the growth plate chondro-osseous junction and in the diaphysis of Osx1Cre.Efnb2Δ/Δ and Efnb2f/f littermates at 2.5-3.5 days of age. *P<0.05 versus Efnb2f/f (large), **P<0.01 versus Efnb2f/f (small). n=6 Efnb2w/w and n=7 Osx1Cre.Efnb2f/f. Scale bars: 50 μm.

Staining for the osteoclastic marker enzyme tartrate-resistant acid phosphatase (TRAP; also known as ACP5) of Osx1Cre.Efnb2Δ/Δ osteoclasts nearer to the growth plate revealed abnormal morphology and less intense TRAP staining compared with controls (Fig. 2B). When quantified at the chondro-osseous junction (Fig. 2C), the total number of osteoclasts was not significantly different between Osx1Cre.Efnb2Δ/Δ and Efnb2f/f controls, but most of the Osx1Cre.Efnb2Δ/Δ osteoclasts on the cartilage surface (chondroclasts) were small and rounded (<15 μm2) (Fig. 2B,C). These small osteoclasts were not observed in sections from control mice, or in the Osx1Cre.Efnb2Δ/Δ metaphysis. On bone surfaces in this region, Osx1Cre.Efnb2Δ/Δ osteoclasts were of normal size and stained intensely for TRAP (Fig. 2C). This suggests altered osteoclast attachment or differentiation in Osx1Cre.Efnb2Δ/Δ mice specifically on cartilage surfaces at the growth plate.

Greater cortical thickness in neonatal Osx1Cre.Efnb2Δ/Δ mice

Analysis by microCT indicated increased material density and greater cortical thickness of the diaphyseal cortical bone in Osx1Cre.Efnb2Δ/Δ femora (Fig. 3A) compared with Efnb2f/f controls. When quantified, expression of the Osx1Cre transgene caused a significantly greater (15%) cortical thickness compared with non-Cre-expressing littermate controls (Fig. 3B). The Osx1Cre.Efnb2Δ/Δ mice showed a still greater cortical thickness than Osx1Cre transgenics (Fig. 3B), indicating either reduced resorption or greater bone formation in the diaphysis of these mice.

Fig. 3.

Increased cortical thickness in Osx1Cre.Efnb2Δ/Δ mice. (A) Images showing X-ray attenuation of 3.5-day-old Efnb2f/f and Osx1Cre.Efnb2Δ/Δ littermates (two per genotype). The scale on the left shows the X-ray attenuation gradient. (B) Mean cortical thickness (Ct.Th) of Osx1Cre.Efnb2Δ/Δ mice (far right bar), littermate Efnb2f/f controls, and age-matched Efnb2w/w and littermate Osx1Cre.Efnb2w/w mice at 2.5-3.5 days of age. Data are the mean percentage of Cre-negative littermate Ct.Th; error bars indicate s.e.m. *P<0.05, ***P<0.001 versus Cre-negative control; #P<0.05 versus Osx1Cre.Efnb2w/w. n=6 Efnb2w/w, n=9 Osx1Cre.Efnb2w/w, n=9 Efnb2f/f and n=6 Osx1Cre.Efnb2f/f.

Fig. 3.

Increased cortical thickness in Osx1Cre.Efnb2Δ/Δ mice. (A) Images showing X-ray attenuation of 3.5-day-old Efnb2f/f and Osx1Cre.Efnb2Δ/Δ littermates (two per genotype). The scale on the left shows the X-ray attenuation gradient. (B) Mean cortical thickness (Ct.Th) of Osx1Cre.Efnb2Δ/Δ mice (far right bar), littermate Efnb2f/f controls, and age-matched Efnb2w/w and littermate Osx1Cre.Efnb2w/w mice at 2.5-3.5 days of age. Data are the mean percentage of Cre-negative littermate Ct.Th; error bars indicate s.e.m. *P<0.05, ***P<0.001 versus Cre-negative control; #P<0.05 versus Osx1Cre.Efnb2w/w. n=6 Efnb2w/w, n=9 Osx1Cre.Efnb2w/w, n=9 Efnb2f/f and n=6 Osx1Cre.Efnb2f/f.

Defective osteoclast and osteoblast morphology visualised by electron microscopy

Electron microscopy of osteoclasts at the chondro-osseous junction confirmed their defective morphology (Fig. 4A,B). Osteoclasts from Osx1Cre.Efnb2Δ/Δ mice showed convoluted nuclear membranes and more heterochromatin than Efnb2w/w, Efnb2f/f and Osx1Cre.Efnb2w/w osteoclasts (Fig. 4A,B). Osx1Cre.Efnb2Δ/Δ osteoclasts were smaller, and their contact with the cartilage matrix was less than that observed in Efnb2w/w, Efnb2f/f and Osx1Cre.Efnb2w/w controls. Sealing zones and ruffled membranes, which form when osteoclasts attach to the bone surface and are required for acidification of the local environment and bone resorption, respectively, were readily observed in Efnb2w/w, Efnb2f/f and Osx1Cre.Efnb2w/w (control) samples (Fig. 4B), but were not detected in Osx1Cre.Efnb2Δ/Δ osteoclasts (Fig. 4B, right). This altered morphology is consistent with impaired resorption.

Fig. 4.

Altered osteoclast and osteoblast attachment to cartilage in Osx1Cre.Efnb2Δ/Δ mice. Electron microscopy images from neonatal controls (Efnb2w/w, Efnb2f/f and Osx1Cre.Efnb2w/w) showing osteoclasts (oc) and their sealing zones (sz) abutting cartilage matrix (cg) (A,B), and osteoblasts (ob) with abundant intercellular attachment and attachment to osteoid (os) on the cartilage surface (C). By contrast (far right), neonatal Osx1Cre.Efnb2Δ/Δ samples (littermates to Osx1Cre.Efnb2w/w) show osteoclasts adjacent to cartilage, their lack of sealing zones, and apoptotic osteoblasts not attached to the bone surface. Scale bars: 1.9 μm in A; 3.3 μm in B; 0.5 μm in C.

Fig. 4.

Altered osteoclast and osteoblast attachment to cartilage in Osx1Cre.Efnb2Δ/Δ mice. Electron microscopy images from neonatal controls (Efnb2w/w, Efnb2f/f and Osx1Cre.Efnb2w/w) showing osteoclasts (oc) and their sealing zones (sz) abutting cartilage matrix (cg) (A,B), and osteoblasts (ob) with abundant intercellular attachment and attachment to osteoid (os) on the cartilage surface (C). By contrast (far right), neonatal Osx1Cre.Efnb2Δ/Δ samples (littermates to Osx1Cre.Efnb2w/w) show osteoclasts adjacent to cartilage, their lack of sealing zones, and apoptotic osteoblasts not attached to the bone surface. Scale bars: 1.9 μm in A; 3.3 μm in B; 0.5 μm in C.

Osteoblast morphology was also notably different in Osx1Cre.Efnb2Δ/Δ mice compared with Efnb2w/w, Efnb2f/f and Osx1Cre.Efnb2w/w controls (Fig. 4C). As previously observed in adult mice (Tonna et al., 2014), osteoblasts from neonatal Osx1Cre.Efnb2Δ/Δ mice displayed very little contact with each other or with the cartilage surface. Neonatal Osx1Cre.Efnb2Δ/Δ osteoblasts also displayed more heterochromatin, less endoplasmic reticulum and more apoptotic osteoblasts than controls, as previously observed (Tonna et al., 2014). All these features of osteoblasts in neonatal Osx1Cre.Efnb2Δ/Δ mice are consistent with impaired function, including the low level of osteoid deposition observed in the neonatal sections.

Reduced support of osteoclast formation by ephrin B2-deficient chondrocytes

To determine whether the impaired osteoclast formation in Osx1Cre.Efnb2Δ/Δ mice resulted from reduced chondrocytic support of osteoclast formation, we co-cultured Osx1Cre.Efnb2Δ/Δ chondrocytes with osteoclast precursors from C57BL/6 mice and treated them with 1,25-dihydroxyvitamin D3 to stimulate osteoclast formation. Osx1Cre.Efnb2Δ/Δ chondrocytes showed a reduced capacity to support osteoclast formation compared with control Efnb2f/f chondrocytes (Fig. 5A), consistent with the defective osteoclast formation observed at the chondro-osseous junction in vivo.

Fig. 5.

Osx1Cre.Efnb2Δ/Δ chondrocytes exhibit less support of osteoclastogenesis and altered gene expression, including low Adamts4. (A) Osteoclasts [TRAP+ were multinucleated cells (MNC)] generated from C57BL/6 bone marrow macrophages cultured with differentiated Efnb2f/f and Osx1Cre.Efnb2Δ/Δ primary chondrocytes and treated with 1,25-dihydroxyvitamin D3. Data are mean±s.e.m. from three independent cultures. (B) Gene expression of Efnb2f/f and Osx1Cre.Efnb2Δ/Δ primary chondrocytes at days 7 and 21 of differentiation. Shown are osterix (Sp7), ephrin B2 (Efnb2), collagen X (Col10a1), osteopontin (Spp1), Adamts4, Adamts5, Rankl (Tnfsf11) and Opg (Tnfrsf11b). Data are the mean±s.e.m. of the ratio to the geometric mean of Hprt1 and B2m from three biological replicates. *P<0.05, ***P<0.001 versus Cre-negative Efnb2f/f cells at the same time point (genotype effect).

Fig. 5.

Osx1Cre.Efnb2Δ/Δ chondrocytes exhibit less support of osteoclastogenesis and altered gene expression, including low Adamts4. (A) Osteoclasts [TRAP+ were multinucleated cells (MNC)] generated from C57BL/6 bone marrow macrophages cultured with differentiated Efnb2f/f and Osx1Cre.Efnb2Δ/Δ primary chondrocytes and treated with 1,25-dihydroxyvitamin D3. Data are mean±s.e.m. from three independent cultures. (B) Gene expression of Efnb2f/f and Osx1Cre.Efnb2Δ/Δ primary chondrocytes at days 7 and 21 of differentiation. Shown are osterix (Sp7), ephrin B2 (Efnb2), collagen X (Col10a1), osteopontin (Spp1), Adamts4, Adamts5, Rankl (Tnfsf11) and Opg (Tnfrsf11b). Data are the mean±s.e.m. of the ratio to the geometric mean of Hprt1 and B2m from three biological replicates. *P<0.05, ***P<0.001 versus Cre-negative Efnb2f/f cells at the same time point (genotype effect).

Altered differentiation of Osx1Cre.Efnb2Δ/Δ chondrocytes

Osx1Cre.Efnb2Δ/Δ chondrocytes showed normal Efnb2 mRNA levels at day 7, but, consistent with increased osterix (Sp7) expression at day 21, Efnb2 mRNA levels at day 21 were significantly lower in Osx1Cre.Efnb2Δ/Δ than in Efnb2f/f chondrocytes (Fig. 5B), consistent with previous reports of Osx1Cre expression in these cells (Rodda and McMahon, 2006; Maes et al., 2010; Chen et al., 2014). Osx1Cre.Efnb2Δ/Δ chondrocytes also showed significantly higher Col10a1 but lower osteopontin (Spp1) mRNA levels at day 21 compared with the Efnb2f/f control, suggesting an alteration in the normal pattern of chondrocytic gene expression in Efnb2-deficient chondrocytes in culture. There was no significant alteration in the mRNA levels of Rankl (Tnfsf11) or its decoy receptor Opg (Tnfrsf11b) (Fig. 5B).

Hypertrophic chondrocytes also promote the destruction of growth plate cartilage by expression of a number of catabolic enzymes, including the matrix metalloproteinases (MMPs) MMP13 (Johansson et al., 1997) and MMP9 (Shinoda et al., 2008; Golovchenko et al., 2013) and the aggrecanases ADAMTS4 and ADAMTS5 (Glasson et al., 2004; Rogerson et al., 2008). We reasoned that, since ephrin B2 deletion was targeted to osteoblasts and chondrocytes, the lack of cartilage destruction in Osx1Cre.Efnb2Δ/Δ mice might relate to reduced production of these proteins by hypertrophic chondrocytes. Whereas no changes in Mmp13, Mmp9 or Adamts5 mRNA were detected (Fig. 5B; data not shown), Adamts4 levels were ∼50% lower in Osx1Cre.Efnb2Δ/Δ cultured chondrocytes at 21 days compared with control (Fig. 5B).

Immunohistochemical staining for ADAMTS4 showed strong staining in resting chondrocytes and osteoblasts in both Osx1Cre.Efnb2Δ/Δ and Efnb2f/f femora and tibiae (distal tibiae shown in Fig. 6A,B). A similar proportion of resting chondrocytes stained positively for ADAMTS4 (Fig. 6C,D), and in both Osx1Cre.Efnb2Δ/Δ and Efnb2f/f femora and tibiae ADAMTS4 was not detected in proliferating chondrocytes. The pattern of ADAMTS4 staining differed in more mature chondrocytes. In Efnb2f/f growth plates, early hypertrophic chondrocytes showed positive intracellular staining for ADAMTS4, whereas late hypertrophic chondrocytes showed little to no stain (Fig. 6E). However, in Osx1Cre.Efnb2Δ/Δ growth plates no ADAMTS4 staining was detected in early hypertrophic chondrocytes, and very few late hypertrophic chondrocytes were positive for this antigen. ADAMTS4 was only detected in those hypertrophic chondrocytes located at the chondro-osseous junction in Osx1Cre.Efnb2Δ/Δ growth plates (Fig. 6F). IgG control sections were clear of staining (Fig. 6G).

Fig. 6.

ADAMTS4 immunohistochemistry in neonatal Efnb2f/f and Osx1Cre.Efnb2Δ/Δ proximal tibiae. (A,C,E,G) Efnb2f/f; (B,D,F) Osx1Cre.Efnb2Δ/Δ. (A,B) Low magnification images showing the overall staining pattern and the regions selected for high magnification. (C,D) Higher magnification images of the upper boxes in A and B, respectively, showing resting and articular chondrocytes. (E,F) Higher magnification images of the lower boxes in A and B, respectively, showing of the base of the proliferating zone through to the chondro-osseous junction. Examples of stained cells are indicated with arrows. (G) IgG control section of an Efnb2f/f femur showing the base of the proliferating zone through to the chondro-osseous junction. Scale bars: 100 μm in A,B; 50 μm in C-G.

Fig. 6.

ADAMTS4 immunohistochemistry in neonatal Efnb2f/f and Osx1Cre.Efnb2Δ/Δ proximal tibiae. (A,C,E,G) Efnb2f/f; (B,D,F) Osx1Cre.Efnb2Δ/Δ. (A,B) Low magnification images showing the overall staining pattern and the regions selected for high magnification. (C,D) Higher magnification images of the upper boxes in A and B, respectively, showing resting and articular chondrocytes. (E,F) Higher magnification images of the lower boxes in A and B, respectively, showing of the base of the proliferating zone through to the chondro-osseous junction. Examples of stained cells are indicated with arrows. (G) IgG control section of an Efnb2f/f femur showing the base of the proliferating zone through to the chondro-osseous junction. Scale bars: 100 μm in A,B; 50 μm in C-G.

Resolution of the osteopetrotic phenotype by 6 weeks of age

We previously reported that 12-week-old Osx1Cre.Efnb2Δ/Δ mice do not exhibit osteopetrosis, suggesting resolution of this phenotype. To determine when this transition occurs, we assessed whether the neonatal osteopetrosis of Osx1Cre.Efnb2Δ/Δ mice was detectable at 6 weeks of age. MicroCT and histomorphometric analysis of Osx1Cre.Efnb2Δ/Δ and Osx1Cre.Efnb2f/f mice at 6 weeks of age revealed no significant differences in trabecular structure or in the numbers of osteoclasts (NOc/BPm) or osteoblasts (NOb/BPm), nor was there any detectable difference in the abundance of cartilage remnants (Table 1). As observed at 12 weeks, the mineral appositional rate was significantly reduced (Table 1), confirming this functional defect in bone mineralisation. Consistent with the resolution of osteopetrosis, no differences were observed in the width of the growth plate [mean growth plate width (μm)±s.e.m. (n=6-9/group): Osx1Cre.Efnb2Δ/Δ, 117±9; Osx1Cre.Efnb2w/w, 109±6], nor of the proliferating or hypertrophic zones [proportion of hypertrophic zone to proliferating zone (%±s.e.m.): Osx1Cre.Efnb2Δ/Δ, 46.7±6.4; Osx1Cre.Efnb2w/w, 43.5±4.9] at 6 weeks of agew/w. Surprisingly, although the osteopetrosis was rescued by this stage of growth, osteoclasts at the chondro-osseous junction still displayed a defective morphology as visualised by electron microscopy (data not shown), further indicating that the defective support of osteoclastogenesis was specific to the growth plate region. At 6 weeks of age, osteoblast morphology was partially recovered compared with control mice, with osteoblasts showing improved attachment to each other; attachment to bone surfaces was still impaired, some osteoblasts showed distended endoplasmic reticulum, and more apoptotic osteoblasts were observed than usual, as previously reported in 9- and 12-week-old mice (Tonna et al., 2014).

Table 1.

Structural and histomorphometric analysis of female 6-week-old Osx1Cre.Efnb2Δ/Δ and Osx1Cre.Efnb2w/w littermates

Structural and histomorphometric analysis of female 6-week-old Osx1Cre.Efnb2Δ/Δ and Osx1Cre.Efnb2w/w littermates
Structural and histomorphometric analysis of female 6-week-old Osx1Cre.Efnb2Δ/Δ and Osx1Cre.Efnb2w/w littermates

This work reveals a novel and necessary function for ephrin B2 signalling in chondrocytes during bone development. The data suggest that ephrin B2 expression by hypertrophic chondrocytes is required for their expression of genes that promote cartilage degradation, such as Adamts4. This preparation of the cartilage matrix might promote the attachment and activity of osteoclasts, which resorb cartilage matrix, and osteoblasts, which form bone on cartilage remnants in vivo. Such a mechanism of cartilage matrix-mediated control of osteoclast attachment might be involved in transient forms of osteopetrosis in the neonatal skeleton and might regulate endochondral fracture healing.

Neonatal Osx1Cre.Efnb2Δ/Δ mice exhibited a significant osteopetrosis that was most notable in the first few days after birth. While chondrocyte morphology appeared normal, the destruction of calcified matrix surrounding hypertrophic chondrocytes was delayed. Impaired destruction of cartilage during endochondral ossification is a hallmark of osteopetrosis, regardless of whether it is caused by impaired osteoclast formation or a defect in osteoclast function (Del Fattore et al., 2008). The combination of a high level of cartilage remnants in the presence of normal osteoclast numbers, as seen in the Osx1Cre.Efnb2Δ/Δ mice, is similar to what has been observed in mice in which osteoclast function is impaired, either due to poor acidification or low enzyme activity, such as in Acp5 (TRAP) (Hayman et al., 1996), Atp6i (Tcirg1) (Li et al., 1999) or Clc7 (Clcn7) (Neutzsky-Wulff et al., 2010) null mice, or when osteoclast attachment is disrupted, as in Src (Soriano et al., 1991) and Pyk2 (Ptk2b) (Gil-Henn et al., 2007) null mice. Cartilage remnants within trabecular bone are also observed in humans with osteopetrosis due to defective osteoclast function (Blair et al., 2009). Since osteoclast number was normal in Osx1Cre.Efnb2Δ/Δ mice, we suggest that ephrin B2 expression in Osx1Cre-expressing cells is required for the normal function of osteoclasts at the developing growth plate.

Defective osteoclast function in these mice was a surprising observation since Efnb2 gene recombination was directed with Osx1Cre, which targets the osteoblast lineage and prehypertrophic and hypertrophic chondrocytes (Rodda and McMahon, 2006; Maes et al., 2010). In these mice, Efnb2 mRNA levels were reduced in osteoblasts (Tonna et al., 2014) and chondrocytes (current work), and we previously confirmed that Efnb2 mRNA levels are not altered in osteoclast precursors or differentiated osteoclasts generated from Osx1Cre.Efnb2Δ/Δ mice (Tonna et al., 2014). This suggests that osteoblasts or chondrocytes that lack ephrin B2 may lack some mechanism of supporting osteoclast activity, particularly near the growth plate. Since the bone matrix is appropriately resorbed as the mice age, we suggest that the defect rests within the mineralised cartilage deposited by ephrin B2-deficient chondrocytes.

Osteoblast attachment observed by electron microscopy of the cartilage remnants was defective in Osx1Cre.Efnb2Δ/Δ mice in neonatal bone, as we previously observed in adults (Tonna et al., 2014). In remodelling trabecular bone, which was assessed in adult Osx1Cre.Efnb2Δ/Δ mice, osteoid volume was significantly increased due to delayed mineralisation (Tonna et al., 2014). By contrast, in the neonatal growth plate, where osteoblasts attach to and form osteoid on a cartilage template, Osx1Cre.Efnb2Δ/Δ osteoblasts showed defective osteoid deposition (Fig. 6). This suggests that the same changes in cartilage composition that impair osteoclast attachment in this region may also impair the attachment and function of osteoblasts. By contrast, during bone remodelling in adult Osx1Cre.Efnb2Δ/Δ mice, osteoblasts work on a bone surface to which they are capable of attaching (Fig. 6); it is their maturation to late stages, including osteocytes, that leads to defective mineralisation of the osteoid, as observed both at 6 and 12 weeks of age.

To determine how chondrocytes support cartilage destruction, we focused on two possible activities: the support of osteoclast formation by Efnb2-deficient chondrocytes, and their expression of cartilage-degrading enzymes. Co-culture of differentiated primary chondrocytes from Osx1Cre.Efnb2Δ/Δ mice showed impaired support of osteoclast formation, as we previously observed with osteoblasts derived from mice of the same genotype (Tonna et al., 2014). This was also consistent with the work of others showing that specific inhibition of the ephrin B2-EPHB4 interaction with the TNYL-RAW peptide inhibited osteoclast formation supported by the ATDC5 chondrocyte cell line (Wang et al., 2014). Surprisingly, mRNA levels for RANKL, a ligand that supports osteoclast formation and is expressed by hypertrophic chondrocytes (Kartsogiannis et al., 1999), and for the RANKL decoy receptor OPG were unchanged. This supports a model whereby the ephrin B2/EPHB4 role in chondrocytic support of osteoclastogenesis is independent of the RANKL/OPG system, as previously suggested (Wang et al., 2014). We hypothesized that enzymatic degradation of the cartilage matrix may also play a role in the osteoclastic destruction of cartilage surrounding hypertrophic chondrocytes.

Chondrocytes from the Osx1Cre.Efnb2Δ/Δ mice exhibited a number of changes in gene expression and an altered pattern of ADAMTS4 staining. Collagen X and osteopontin levels normally increase with chondrocyte hypertrophy (Lian et al., 1993), but their co-regulation was disrupted in Osx1Cre.Efnb2Δ/Δ chondrocytes: Col10a1 levels were elevated but osteopontin levels were reduced, suggesting disruption of the normal profile of hypertrophic gene expression. Since Adamts4 is upregulated in hypertrophic chondrocytes (Lian et al., 1993; Glasson et al., 2004), the low level of Adamts4 mRNA that we observe in Osx1Cre.Efnb2Δ/Δ chondrocytes is more likely to reflect a delay in chondrocyte hypertrophy in the absence of ephrin B2 than direct regulation by osteopontin, particularly since exogenous treatment with this protein is reported to suppress Adamts4 expression (Gao et al., 2015). A full understanding of the changes in gene expression in Osx1Cre.Efnb2Δ/Δ chondrocytes would require a non-biased approach, such as a microarray study of micro-dissected mRNA from these mutant growth plates.

Hypertrophic chondrocytes also express metalloproteinases and aggrecanases (Johansson et al., 1997; Glasson et al., 2004; Shinoda et al., 2008; Golovchenko et al., 2013) and there are several lines of evidence indicating that these regulate osteoclast activity during endochondral ossification. Mice carrying a collagen mutation rendering it resistant to collagenases show impaired osteoclastic resorption of growth plate cartilage (Chiusaroli et al., 2003), while Mmp13 null mice show impaired osteoclast attachment in endochondral fracture healing (Holliday et al., 1997; Kosaki et al., 2007). ADAMTS4 has previously been detected in hypertrophic chondrocytes at the growth plate of adult mice (Glasson et al., 2004), in osteoblasts in developing limbs (Nakamura et al., 2005) and is elevated during endochondral fracture healing (Wang et al., 2006). Our detection of ADAMTS4 in ∼60% of resting chondrocytes and in early hypertrophic chondrocytes suggests that it may play a role in degradation of the cartilage matrix during neonatal bone development.

In cultured ephrin B2-deficient chondrocytes we observed significantly lower Adamts4 mRNA levels compared with control cells at day 21 of differentiation. Although ADAMTS4 immunohistochemical staining was strong in osteoblasts and in a proportion of resting chondrocytes in Osx1Cre.Efnb2Δ/Δ limbs, no clear ADAMTS4 staining was detected in early hypertrophic chondrocytes. By contrast, only hypertrophic chondrocytes at the chondro-osseous junction were positive for ADAMTS4. This provides another indication of altered chondrocyte differentiation, and suggests that delayed ADAMTS4 expression may play a role in the impaired cartilage degradation/resorption in the absence of ephrin B2. Although mice deficient in Adamts4 have previously been reported to have no gross developmental defect (Glasson et al., 2004), a phenotype such as that we describe here in Osx1Cre.Efnb2Δ/Δ mice would not be detected by a screen for gross morphological changes.

Our findings suggest that cartilage degradation by chondrocytes is required to prepare the cartilage matrix for osteoclast attachment and resorptive activity. This is consistent with similar activities in bone, where collagenase prepares bone surfaces for osteoclastic attachment and subsequent resorption (Chambers et al., 1985; Chambers and Fuller, 1985). Several outcomes of this action have been proposed: first, that osteoclasts attach more strongly to degraded collagen matrix; second, that fragments of degraded collagen ‘activate’ osteoclasts to resorb bone (Holliday et al., 1997). We suggest that similar mechanisms, initiated by chondrocytic enzyme production, may play a similar role to mediate osteoclast attachment to growth plate cartilage in the hypertrophic zone.

The osteopetrosis of neonatal Osx1Cre.Efnb2Δ/Δ mice had fully resolved by 6 weeks of age, consistent with our previous observation that 12-week-old Osx1Cre.Efnb2Δ/Δ mice have normal trabecular bone mass (Tonna et al., 2014). Osteopetrosis varies widely in its aetiology, and forms that resolve before puberty have been described in rats and human (Marks, 1973; Monaghan et al., 1991; Cielinski and Marks, 1995; Del Fattore et al., 2008), although no mechanism for this spontaneous resolution is known. One common element of these self-resolving forms of osteopetrosis is a defect in osteoclast enzyme function. The low level of TRAP staining observed in Osx1Cre.Efnb2Δ/Δ osteoclasts on cartilage is consistent with this, and the altered osteoclast morphology is strikingly similar to observations made in the transient osteopetrosis of the microphthalmia rat model (Cielinski and Marks, 1994). Notably, TRAP staining in the diaphysis, where osteoclasts attach to bone, was normal, consistent with previous observations in adult mice (Tonna et al., 2014). Thus, the resolution of transient osteopetrosis in humans and other mammals might be explained by the lesser contribution of resorption of growth plate cartilage to trabecular bone mass with age, as longitudinal growth declines.

The contrast between the normal trabecular bone mass at 6 weeks and the development of a high-bone-mass phenotype in female Osx1Cre.Efnb2Δ/Δ mice at 26 weeks of age (Tonna et al., 2014) is also likely to relate to altered contributions of endochondral ossification and bone remodelling to trabecular bone mass with age (Fig. 7). Trabecular bone mass in neonatal mice reflects the process of endochondral ossification, where resorption of cartilage templates is necessary for subsequent osteoblast-mediated bone formation. Impaired osteoclast activity at this age leads to osteopetrosis, characterised by high trabecular number but low trabecular thickness. In the adult mouse, as well as the contribution of endochondral ossification to bone mass being lower, trabecular bone mass is measured in the secondary spongiosa. This region does not exist in the neonatal mouse, and its trabecular bone volume depends on the balance between bone formation by osteoblasts and bone resorption by osteoclasts. During the transition period (6 and 12 weeks of age), both endochondral ossification and remodelling contribute to bone mass. We suggest that, in the Osx1Cre.Efnb2Δ/Δ mice, the low level of osteoid deposition on the cartilage template leads to normal trabecular bone mass by 6 weeks of age. In the secondary spongiosa of 12-week-old Osx1Cre.Efnb2Δ/Δ mice, osteoclast numbers are low and bone mineralisation is delayed, with a slight imbalance leading to a gradual accumulation of bone mass in this region that is not detected until 26 weeks of age. A phenotype with different effects on bone mass in the primary versus the secondary spongiosa, due to different control mechanisms in these regions, has been reported previously (Poulton et al., 2012).

Fig. 7.

Phenotypic differences between neonatal and adult Osx1Cre.Efnb2Δ/Δ mice. (A) In neonatal mice, osteoclasts resorb cartilage (orange) surrounding the hypertrophic chondrocytes, and osteoblasts lay down new osteoid on template that remains for the trabecular network. (B) In neonatal Osx1Cre.Efnb2Δ/Δ mice, osteoclast and osteoblast attachment to the cartilage surface is defective. Defective osteoclast activity leads to an increase in cartilage remnants and a high volume of mineralised bone and cartilage. In addition, owing to poor osteoblast attachment and apoptosis (shaded cells), very little osteoid is deposited. (C) In trabecular remodelling – a process that occurs in the secondary spongiosa (red box) – osteoclast and osteoblast activities determine trabecular structure. (D) In adult Osx1Cre.Efnb2Δ/Δ mice there are fewer osteoclasts. This lack of resorption, and defective mineralisation caused by osteoblast and osteocyte apoptosis (shaded cells), were associated with a gradual accumulation of trabecular bone.

Fig. 7.

Phenotypic differences between neonatal and adult Osx1Cre.Efnb2Δ/Δ mice. (A) In neonatal mice, osteoclasts resorb cartilage (orange) surrounding the hypertrophic chondrocytes, and osteoblasts lay down new osteoid on template that remains for the trabecular network. (B) In neonatal Osx1Cre.Efnb2Δ/Δ mice, osteoclast and osteoblast attachment to the cartilage surface is defective. Defective osteoclast activity leads to an increase in cartilage remnants and a high volume of mineralised bone and cartilage. In addition, owing to poor osteoblast attachment and apoptosis (shaded cells), very little osteoid is deposited. (C) In trabecular remodelling – a process that occurs in the secondary spongiosa (red box) – osteoclast and osteoblast activities determine trabecular structure. (D) In adult Osx1Cre.Efnb2Δ/Δ mice there are fewer osteoclasts. This lack of resorption, and defective mineralisation caused by osteoblast and osteocyte apoptosis (shaded cells), were associated with a gradual accumulation of trabecular bone.

Another region in which the bone phenotype differed significantly between the adult and neonatal mouse was the cortical bone. Neonatal Osx1Cre.Efnb2Δ/Δ mice showed thicker cortical bone than their control littermates, but by 6 weeks of age the cortical thickness was low due to impaired periosteal expansion. The latter finding is consistent with our previous observations in older adult mice (Tonna et al., 2014). During bone development the cortical bone forms and narrows as osteoclasts resorb cartilage from the centre of the anlagen. Impaired osteoclast activity, as observed in neonatal Osx1Cre.Efnb2Δ/Δ mice, results in a lack of resorption of the primary ossification centre and a delay in the reduction of cortical width. As the mice age, cortical bone thickens through periosteal growth, a process that is impaired in Osx1Cre.Efnb2Δ/Δ mice. As in the trabecular bone, cortical bone development and cortical expansion are differently affected by the deletion of ephrin B2 in osteoblasts and chondrocytes.

Ephrin B2 is thought to depend on cell-cell contact for signalling (Pasquale, 2010). Although extensive cell-cell contact exists within the osteocyte network (Buenzli and Sims, 2015) and between bone-forming osteoblasts, and contact-dependent mechanisms are recognised to control bone formation (Tonna and Sims, 2014), it is not clear how membrane-bound ephrin B2 could influence cell function in chondrocytes since these cells are isolated from each other by the cartilaginous matrix. There are two possibilities: ephrin B2 might be capable of autocrine signalling through EPHB4, which is also expressed by hypertrophic chondrocytes (Wang et al., 2014); alternatively, there might be cell-cell contact between hypertrophic chondrocytes. However, although prehypertrophic chondrocytes express the gap junction components connexin 43 (Gja1) and pannexin 3 (Schwab et al., 1998; Iwamoto et al., 2010; Bond et al., 2011), gap junctions between growth plate chondrocytes have not been observed in situ.

In conclusion, Osx1Cre-targeted deletion of ephrin B2 results in a transient neonatal osteopetrosis caused by a region-specific defect in osteoclast attachment and activity. This points to a role for cartilage-specific factors, including ADAMTS4, in controlling osteoclastic resorption during endochondral bone development.

Animals

Animal procedures were approved by the St Vincent's Health Melbourne Animal Ethics Committee. Tg(Sp7-tTA,tetO-EGFP/cre)1Amc (Osx1-GFP::Cre) mice backcrossed onto C57BL/6 were generated as previously described (Tonna et al., 2014) by crossing Tg(Sp7-tTA,tetO-EGFP/cre)1Amc (Rodda and McMahon, 2006) and Efnb2tm1And mice (Gerety and Anderson, 2002). Except where noted, all controls are littermates, since neonatal mice change their bone structure in a matter of hours. Since perinatal mice grow rapidly, and the Osx1Cre transgene has been reported to influence bone structure (Davey et al., 2012; Huang and Olsen, 2015), three parallel breeding colonies were used: (1) Efnb2f/f breeders hemizygous for Osx1Cre, to provide neonatal Osx1Cre.Efnb2Δ/Δ and Efnb2f/f littermates; (2) wild-type breeders from the same colony that were hemizygous for Osx1Cre, to provide neonatal Osx1Cre.Efnb2w/w and wild-type littermates; and (3) Osx1Cre.Efnb2w/f breeders to generate Osx1Cre.Efnb2Δ/Δ and Osx1Cre.Efnb2w/w littermates for analysis at 6 weeks of age. For chondrocyte cultures, breeding colony 1 was used as the most practical way to provide littermate controls and limit wastage of animals; the lack of Osx1Cre.Efnb2w/w littermate cultures might limit the interpretation of those data.

Histology and histomorphometry

Neonatal hind leg and 6-week-old tibia samples were fixed in 4% paraformaldehyde and embedded in methylmethacrylate (Sims et al., 2000) and 5 µm sections were stained with von Kossa, Toluidine Blue, Xylenol Orange or Safranin O/Fast Green as previously described (Poulton et al., 2012). Histomorphometric analysis using OsteoMeasure (OsteoMetrics) was carried out in the proximal tibia, commencing 370 µm from the start of the mineralising zone of the growth plate on Toluidine Blue-stained sections, as previously described (Walker et al., 2008). For analysis of neonatal mice, to correct for slight differences in age that may exist between the litters, all histomorphometric data are presented as a percentage of data obtained from Osx1Cre-negative littermate controls. Since Osx1Cre mice have been reported to exhibit a neonatal phenotype (Huang and Olsen, 2015), we also examined age-matched wild-type and Osx1Cre littermates. Hypertrophic zone width was measured at the centre of the distal femoral growth plates; two sections per mouse were evaluated across 370 μm, avoiding the sides closest to the edge of the bone. No significant alterations in raw BV/TV values were observed between Efnb2-loxP mice and age-matched wild-type controls (data not shown). All histomorphometric data include all mice (at least one per genotype per litter) from three litters; n=5-9 per group, including a mixture of male and female neonatal mice.

Micro-computed tomography (microCT)

Ex vivo microCT was performed on femoral specimens using a SkyScan 1076 system (Bruker). Images were acquired with a 0.5 mm aluminium filter at 9 μm pixel size, 50 kV and 100 μA. Houndsfield unit (HU) calibration setting was 125,000 and rotation 0.5°. For neonatal bones, images were reconstructed using NRecon (version 1.6.3.1) with a dynamic image range of 0-0.06. DataViewer (version 1.4.4) was used to reorient images, and pseudocoloured images of the whole femur were obtained by volume rendering (CTvox version 2.4.0). The transfer function components (red, green, blue and opacity) were adjusted to the same settings for all samples. CTan (version 1.11.8.0) was used for femoral trabecular analysis; the trabecular region of interest (ROI) was taken as 20% of the total bone length commencing at a site 40% proximal to the distal end. For samples from 6-week-old mice, microCT of the distal femora was performed as previously described (Takyar et al., 2013).

Immunohistochemistry

Hindlimbs from neonatal mice were fixed, decalcified and embedded in paraffin and used for immunohistochemistry as previously described (Sims et al., 1997) with the following modifications. Endogenous peroxidase was inhibited with 0.3% hydrogen peroxide (Merck) in PBS for 30 min, then blocked with 5% normal goat serum in 1% BSA/PBS. Sections were incubated overnight with 1:100 rabbit anti-ADAMTS4 (ab28285, Abcam) in 1% BSA/PBS, followed by 6 µg/ml biotinylated goat anti-rabbit IgG (DakoCytomation) for 1 h and 1.6 mg/ml streptavidin-HRP (DakoCytomation) in PBS for 30 min. ADAMTS4-positive cells were visualised with 0.5 mg/ml diaminobenzidine (Sigma) in PBS, then lightly counterstained with Haematoxylin before dehydration and coverslipping. Four hindlimb sections of each genotype, including both femur and tibia, from two independent litters were assessed. Immunohistochemical staining was carried out on two separate occasions on all sections, and IgG controls were included.

Electron microscopy

Femurs from 1.5- to 2.5-day-old Efnb2w/w, Efnb2f/f, Osx1Cre.Efnb2Δ/Δ and Osx1Cre.Efnb2w/w mice (n=3 each) were fixed for a minimum of 24 h in Karnovsky's fixative. Samples were post-fixed in 1% osmium tetroxide/1.5% potassium ferrocyanide for 5 h and embedded in Spurr's resin. Ultrathin sections were stained with uranyl acetate/Reynold's lead citrate and examined with a Philips 300 transmission electron microscope at 60 kV as previously described (Tonna et al., 2014).

Primary chondrocytes

Primary chondrocytes were generated from the rib cages of 2.5- to 4.5-day-old Osx1Cre.Efnb2Δ/Δ and Efnb2f/f littermates using previously described methods (Gosset et al., 2008), with the following modifications. The immature chondrocytes were seeded at a density of 30,000 cells/well into a 3.5 cm plate (Corning) in complete medium (DMEM+10% FBS) and left overnight at 37°C in 5% CO2. The following day, the plates were placed in 1% O2, 5% CO2 and 94% N2 within a sealed hypoxia chamber (Billups-Rothenberg) at 37°C. Cells were then differentiated for 21 days in chondrocyte differentiation media (Gosset et al., 2008).

Chondrocytic support of osteoclast formation was assessed by co-culture of primary chondrocytes and bone marrow macrophages from C57BL/6 mice (Masuyama et al., 2006) using primary chondrocytes generated as above. To ensure that ephrin B2 had been downregulated, chondrocytes were first differentiated in chondrocyte differentiation media for 21 days at 1% O2, 5% CO2 and 94% N2, as above, then transferred to 37°C under 5% CO2 for co-culture with bone marrow macrophages.

RNA extraction and RT-PCR

Total RNA was extracted from primary chondrocytes and quantitative RT-PCR was performed using previously described methods (Tonna et al., 2014). Primers are listed in Table S1. Data shown in Fig. 5B were calculated by normalising to the geometric mean of the two housekeeping genes Hprt1 and B2m using the ΔCt method, and fold-change calculations using the ΔΔCt method were performed as previously described (Chia et al., 2015).

Statistical methods

All statistical tests were carried out using Prism 6. Data shown in Fig. 1B, Fig. 3B and Fig. 5B were analysed by two-way ANOVA. Data shown in Fig. 2C, Fig. 5A and Table 2 were analysed by Student's t-test. P<0.05 was considered significant.

Author contributions

S.T., I.J.P., F.T., B.C.-I., N.E.M., B.T., P.W.M.H., L.T. and N.A.S. conducted experiments and analysed data. S.T., N.A.S., L.T., E.J.M. and T.J.M. designed experiments and interpreted data. The manuscript was prepared by S.T. and N.A.S., and edited by S.T., N.A.S., E.J.M. and T.J.M. All authors read and approved the final manuscript.

Funding

This work was supported by National Health and Medical Research Council (Australia) (NHMRC) Project Grants [620200 and 104129]. N.A.S. is supported by an NHMRC Senior Research Fellowship. S.T. received support from an NHMRC Peter Doherty Early Career Fellowship. The Victorian State Government Operational Infrastructure Support Scheme provides support to St Vincent's Institute.

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Competing interests

The authors declare no competing or financial interests.

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