Completed Cells, Biochemistry & Physiology Genetics & Molecular Biology

Development of the Xenopus and Zebrafish Retina.

In plain English

AI plain-English summary

A developing tadpole or zebrafish embryo builds a working retina in days, and this project tracks exactly how it does so—cell by cell, signal by signal. The research addresses a fundamental gap in neuroscience: how a sheet of uncommitted embryonic tissue transforms into a precisely layered, light-sensitive retina. The team will map the signalling pathways—particularly Hedgehog and Wnt—that orchestrate this process, and use live imaging to trace individual neural lineages as they form. They will also investigate how Zic transcription factors control cell proliferation and patterning in the optic cup, and how interkinetic nuclear migration drives the behaviour of dividing neuroepithelial cells. This is fundamental science, not applied medicine. There is no immediate clinical or commercial application. But understanding how a vertebrate retina assembles from scratch provides a blueprint for neural development more broadly. Similar work on embryonic patterning has already informed stem-cell protocols for growing retinal tissue in a dish. If this project succeeds, it will clarify the rules that govern how stem cells commit to specific fates and organise into functional neural circuits—knowledge that could eventually guide efforts to repair damaged retinas or engineer neural tissue for transplantation.

View original technical description
The proposed research on mechanisms of neural development, uses the Xenopus and zebrafish retina as model systems. The key goals of this programme of work are: 1. To investigate the embryonic origins of the retina and in particular to elucidate the signalling pathways involved in the multistage induction of the eyefield from uncommitted and multipotent ectodermal tissue. 2. To characterize the role of the Zic transcription factors in optic cup proliferation and patterning, and to underst and the interaction of Zic proteins as putative integrators of Hedgehog and Wnt signalling in this process. 3. To probe the mechanisms of interkinetic nuclear migration that characterizes proliferating neuroepithelial cells in the retina. 4. To uncover the mechanism by which Hedgehog and Wnt signaling participate in the transition from slow dividing undetermined retinal stem cells to rapidly dividing neural precursors. 5. To extend our knowledge of how specific neurons arise in the reti na by tracing distinct lineages in real time with dynamic imaging in normal and mutant environments. This work continues our longstanding commitment to take advantage of the remarkable opportunities that the vertebrate retina in these model systems provides to open up new issues in the general field of neural development.

View the original record at the funder ↗

Researchers

William Harris (EPMC Awardee)

Related Research

Grants with similar aims, by meaning.

Understanding the mechanism of vision development
Morphogenesis and growth of the eye in health and disease
Epithelial fusion during optic fissure closure in zebrafish eye development.
The zebrafish tectal stem cell niche - a new model for in vivo analysis of neural stem cell biology
Modelling retinal disease mechanisms and ocular cell development

Original classification

Programme Grant

Plain English summaries and category classifications on this site are generated by AI and may not perfectly reflect the original research.