Abstract

The emergence of retinal progenitor cells and differentiation to various retinal cell types represent fundamental processes during retinal development. Herein, we provide a comprehensive single cell characterisation of transcriptional and chromatin accessibility changes that underline retinal progenitor cell specification and differentiation over the course of human retinal development up to midgestation. Our lineage trajectory data demonstrate the presence of early retinal progenitors, which transit to late, and further to transient neurogenic progenitors, that give rise to all the retinal neurons. Combining single cell RNA-Seq with spatial transcriptomics of early eye samples, we demonstrate the transient presence of early retinal progenitors in the ciliary margin zone with decreasing occurrence from 8 post-conception week of human development. In retinal progenitor cells, we identified a significant enrichment for transcriptional enhanced associate domain transcription factor binding motifs, which when inhibited led to loss of cycling progenitors and retinal identity in pluripotent stem cell derived organoids.

Formation of the retina during development involves the coordinated action of retinal progenitor cells and their differentiated cell types, which is key for producing a functioning eye. Here the authors provide a detailed atlas of human retinal development, combining scRNA-seq and spatial transcriptomics, and identify key genetic factors that mediate retinal progenitor cell proliferation and differentiation.

Details

Title
Single-cell analyses reveal transient retinal progenitor cells in the ciliary margin of developing human retina
Author
Dorgau, Birthe 1 ; Collin, Joseph 1 ; Rozanska, Agata 1 ; Zerti, Darin 2 ; Unsworth, Adrienne 1   VIAFID ORCID Logo  ; Crosier, Moira 1 ; Hussain, Rafiqul 1 ; Coxhead, Jonathan 1 ; Dhanaseelan, Tamil 1 ; Patel, Aara 3 ; Sowden, Jane C. 3 ; FitzPatrick, David R. 4   VIAFID ORCID Logo  ; Queen, Rachel 1 ; Lako, Majlinda 1   VIAFID ORCID Logo 

 Newcastle University, Biosciences Institute, Newcastle, UK (GRID:grid.1006.7) (ISNI:0000 0001 0462 7212) 
 Newcastle University, Biosciences Institute, Newcastle, UK (GRID:grid.1006.7) (ISNI:0000 0001 0462 7212); University of L’Aquila, Department of Biotechnological and Applied Clinical Sciences, L’Aquila, Italy (GRID:grid.158820.6) (ISNI:0000 0004 1757 2611) 
 University College London, UCL Great Ormond Street Institute of Child Health and NIHR Great Ormond Street Hospital Biomedical Research Centre, London, UK (GRID:grid.83440.3b) (ISNI:0000000121901201) 
 University of Edinburgh, MRC Human Genetics Unit, Institute of Genetics and Cancer, Edinburgh, UK (GRID:grid.4305.2) (ISNI:0000 0004 1936 7988) 
Pages
3567
Publication year
2024
Publication date
2024
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
3046998230
Copyright
© The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.