Issues
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Cover image
Cover Image
Cover: Mouse blastocysts were cultured and trophoectoderm was differentiated to highly polyploid trophoblast giant cells. Trophoblast giant cells are stained to visualize DNA (DAPI/yellow), lamin B1 (cyan) and α-tubulin (purple). Lamin B1 staining may be non-specific outside the nucleus. See Research article by Singh et al. (dev201581).
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RESEARCH HIGHLIGHTS
INTERVIEW
SPOTLIGHTS
Technical challenges of studying early human development
Summary: Identifying technical challenges of studying human development, and potential solutions to those obstacles, provides a framework for the research community to help advance knowledge and application of human developmental biology.
Maturing differentiated human pluripotent stem cells in vitro: methods and challenges
Summary: A Spotlight on the challenges of maturing cells that are differentiated from human pluripotent stem cells in vitro, discussing methods to drive cardiomyocyte maturation, as an example.
MEETING REVIEW
Developmental mechanisms understood quantitatively
Summary: A review of The Company of Biologists workshop ‘Fostering quantitative modelling and experimentation in Developmental Biology’, held in July 2022.
HUMAN DEVELOPMENT
RTK signalling promotes epithelial columnar cell shape and apical junction maintenance in human lung progenitor cells
Summary: A self-renewing organoid system reveals that the shape and junctional structure of human lung epithelial progenitor cells during branching are controlled by MAPK/ERK and PI3K/AKT signalling.
RESEARCH REPORT
OptIC-Notch reveals mechanism that regulates receptor interactions with CSL
Highlighted Article: Light-controlled exposure of the Notch ΦWΦP motif leads to CSL sequestration in Drosophila, suggesting that this interaction could occur prior to nuclear entry during normal signalling.
RESEARCH ARTICLES
Myc promotes polyploidy in murine trophoblast cells and suppresses senescence
Highlighted Article: Polyploidy is widespread in murine placental cell types. The transcription factor MYC supports polyploidy and prevents premature senescence in trophoblast giant cells.
Aquaporin regulates cell rounding through vacuole formation during endothelial-to-hematopoietic transition
Highlighted Article: The characterization of vacuoles in chick and quail hemogenic endothelial cells, and the analysis of aquaporin localization suggest that endothelial cell rounding by water permeation is regulated by aquaporin.
Inhibitory SMAD6 interferes with BMP-dependent generation of muscle progenitor cells and perturbs proximodistal pattern of murine limb muscles
Summary: Abrogation of BMP signaling in early murine embryonic limb muscle precursors impaired their migration and proliferation, accelerated myogenic lineage progression and caused an aberrant proximodistal muscle pattern.
Notch directs telencephalic development and controls neocortical neuron fate determination by regulating microRNA levels
Summary: Notch signaling promotes the neurogenesis of late-born cortical fates in mouse brain by upregulating the microRNAs let-7, miR-99a/100 and miR-125b.
A dynamical systems treatment of transcriptomic trajectories in hematopoiesis
Highlighted Article: Bridging the mathematical theory of dynamical systems and high-dimensional transcriptomic data of differentiating cells by studying statistical signatures of linear instability, encoded in a time-varying covariance matrix.
Stuxnet fine-tunes Notch dose during development using a functional Polycomb response element
Summary: Studying the role of the epigenetic regulator Stuxnet in Drosophila developmental signaling reveals that it promotes Notch receptor mRNA expression by counteracting the activity of Polycomb repressive complex 1.
Normal cell cycle progression requires negative regulation of E2F1 by Groucho during S phase and its relief at G2 phase
Summary: Groucho switches between active and inactive states during the cell cycle, and restricts gene expression in a phase-specific manner; relief of its repression is required for progression through G2 phase.
TECHNIQUES AND RESOURCES
CIARA: a cluster-independent algorithm for identifying markers of rare cell types from single-cell sequencing data
Summary: The CIARA algorithm robustly identifies rare cell types and their markers across multiple modalities of single-cell sequencing data.
Interviews with Biologists @ 100 conference speakers

Explore our interviews with keynote speakers from the Biologists @ 100 conference, hosted to celebrate our publisher’s 100th anniversary, where we discuss climate change and biodiversity with Hans-Otto Pörtner and Jane Francis, health and disease with Charles Swanton and Sadaf Farooqi, and emerging technologies with Manu Prakash and Jennifer Lippincott-Schwartz.
Call for papers – Lifelong Development: the Maintenance, Regeneration and Plasticity of Tissues

Development invites you to submit your latest research to our upcoming special issue – Lifelong Development: the Maintenance, Regeneration and Plasticity of Tissues. This issue will be coordinated by Guest Editors Meritxell Huch (Max Planck Institute of Molecular Cell Biology and Genetics, Germany) and Mansi Srivastava (Harvard University and Museum of Comparative Zoology, USA), working alongside our team of academic Editors. Submit your articles by 30 May 2025.
A case for broadening our view of mechanism in developmental biology

In this Perspective, B. Duygu Özpolat and colleagues survey researchers on their views on what it takes to infer mechanism in developmental biology. They examine what factors shape our idea of what we mean by ‘mechanism’ and suggest a path forward that embraces a broad outlook on the diversity of studies that advance knowledge in our field.
In preprints
Did you know that Development publishes perspectives on recent preprints? These articles help our readers navigate the ever-growing preprint literature. Together with our preprint highlights service, preLights, these perspectives help our readers navigate the ever-growing preprint literature. We welcome proposals for ‘In preprints’ articles, so please do get in touch if you’d like to contribute.
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