Single-cell analyses reveal transient retinal progenitor cells in the ciliary margin of developing human retina.
Birthe DorgauJoseph CollinAgata RozanskaDarin ZertiAdrienne UnsworthMoira CrosierRafiqul HussainJonathan CoxheadTamil DhanaseelanAara PatelJane C SowdenDavid R FitzPatrickRachel QueenMajlinda LakoPublished in: Nature communications (2024)
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.
Keyphrases
- single cell
- optical coherence tomography
- diabetic retinopathy
- rna seq
- optic nerve
- transcription factor
- endothelial cells
- gene expression
- high throughput
- spinal cord
- randomized controlled trial
- clinical trial
- machine learning
- risk assessment
- dna methylation
- induced pluripotent stem cells
- bone marrow
- mesenchymal stem cells
- cell therapy
- heat stress
- high intensity
- light emitting