类有机物
生物
电池类型
视网膜
细胞生物学
细胞
分辨率(逻辑)
计算生物学
神经科学
遗传学
计算机科学
人工智能
作者
Cameron S. Cowan,Magdalena Renner,Martina De Gennaro,Brigitte Gross-Scherf,David Goldblum,Yanyan Hou,Martin Munz,Tiago M. Rodrigues,Jacek Król,Tamás Szikra,Rachel Cuttat,Annick Waldt,Panagiotis Papasaikas,Roland Diggelmann,Claudia P. Patino-Alvarez,Patricia Galliker,Stefan E. Spirig,Dinko Pavlinić,Nadine Gerber-Hollbach,Sven Schuierer
出处
期刊:Cell
[Cell Press]
日期:2020-09-01
卷期号:182 (6): 1623-1640.e34
被引量:507
标识
DOI:10.1016/j.cell.2020.08.013
摘要
Human organoids recapitulating the cell-type diversity and function of their target organ are valuable for basic and translational research. We developed light-sensitive human retinal organoids with multiple nuclear and synaptic layers and functional synapses. We sequenced the RNA of 285,441 single cells from these organoids at seven developmental time points and from the periphery, fovea, pigment epithelium and choroid of light-responsive adult human retinas, and performed histochemistry. Cell types in organoids matured in vitro to a stable "developed" state at a rate similar to human retina development in vivo. Transcriptomes of organoid cell types converged toward the transcriptomes of adult peripheral retinal cell types. Expression of disease-associated genes was cell-type-specific in adult retina, and cell-type specificity was retained in organoids. We implicate unexpected cell types in diseases such as macular degeneration. This resource identifies cellular targets for studying disease mechanisms in organoids and for targeted repair in human retinas.
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