State Key Laboratory of Brain and Cognitive Science, Institute of Biophysics, Chinese Academy of Sciences, Beijing 100101, China; University of Chinese Academy of Sciences, Beijing 100049, China.
John F. Hardesty, MD, Department of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, MO 63110, USA.
Dev Cell. 2020 May 18;53(4):473-491.e9. doi: 10.1016/j.devcel.2020.04.009. Epub 2020 May 7.
The development of single-cell RNA sequencing (scRNA-seq) has allowed high-resolution analysis of cell-type diversity and transcriptional networks controlling cell-fate specification. To identify the transcriptional networks governing human retinal development, we performed scRNA-seq analysis on 16 time points from developing retina as well as four early stages of retinal organoid differentiation. We identified evolutionarily conserved patterns of gene expression during retinal progenitor maturation and specification of all seven major retinal cell types. Furthermore, we identified gene-expression differences between developing macula and periphery and between distinct populations of horizontal cells. We also identified species-specific patterns of gene expression during human and mouse retinal development. Finally, we identified an unexpected role for ATOH7 expression in regulation of photoreceptor specification during late retinogenesis. These results provide a roadmap to future studies of human retinal development and may help guide the design of cell-based therapies for treating retinal dystrophies.
单细胞 RNA 测序 (scRNA-seq) 的发展使得对细胞类型多样性和控制细胞命运特化的转录网络进行高分辨率分析成为可能。为了鉴定控制人类视网膜发育的转录网络,我们对来自发育中的视网膜以及视网膜类器官分化的四个早期阶段的 16 个时间点进行了 scRNA-seq 分析。我们鉴定了在视网膜祖细胞成熟和所有七种主要视网膜细胞类型的特化过程中保守的基因表达模式。此外,我们还鉴定了发育中的黄斑和周边之间以及水平细胞不同群体之间的基因表达差异。我们还在人和小鼠视网膜发育过程中鉴定了物种特异性的基因表达模式。最后,我们鉴定了 ATOH7 表达在晚期视网膜发生过程中对光感受器特化的调控中的意外作用。这些结果为未来的人类视网膜发育研究提供了路线图,并可能有助于指导用于治疗视网膜营养不良的基于细胞的治疗方法的设计。