Single-cell RNA sequencing in vision research: Insights into human retinal health and disease

生物 视网膜 诱导多能干细胞 计算生物学 电池类型 基因表达 视网膜 细胞 核糖核酸 黄斑变性 视网膜色素上皮 基因 遗传学 神经科学 胚胎干细胞 医学 眼科 生物化学
作者
Andrew P. Voigt,Nathaniel K. Mullin,Edwin M. Stone,Budd A. Tucker,Todd E. Scheetz,Robert F. Mullins
出处
期刊:Progress in Retinal and Eye Research [Elsevier]
卷期号:83: 100934-100934 被引量:30
标识
DOI:10.1016/j.preteyeres.2020.100934
摘要

Gene expression provides valuable insight into cell function. As such, vision researchers have frequently employed gene expression studies to better understand retinal physiology and disease. With the advent of single-cell RNA sequencing, expression experiments provide an unparalleled resolution of information. Instead of studying aggregated gene expression across all cells in a heterogenous tissue, single-cell technology maps RNA to an individual cell, which facilitates grouping of retinal and choroidal cell types for further study. Single-cell RNA sequencing has been quickly adopted by both basic and translational vision researchers, and single-cell level gene expression has been studied in the visual systems of animal models, retinal organoids, and primary human retina, RPE, and choroid. These experiments have generated detailed atlases of gene expression and identified new retinal cell types. Likewise, single-cell RNA sequencing investigations have characterized how gene expression changes in the setting of many retinal diseases, including how choroidal endothelial cells are altered in age-related macular degeneration. In addition, this technology has allowed vision researchers to discover drivers of retinal development and model rare retinal diseases with induced pluripotent stem cells. In this review, we will overview the growing number of single-cell RNA sequencing studies in the field of vision research. We will summarize experimental considerations for designing single-cell RNA sequencing experiments and highlight important advancements in retinal, RPE, choroidal, and retinal organoid biology driven by this technology. Finally, we generalize these findings to genes involved in retinal degeneration and outline the future of single-cell expression experiments in studying retinal disease.
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