Author:
Cowan Cameron S.,Renner Magdalena,Gross-Scherf Brigitte,Goldblum David,Munz Martin,Krol Jacek,Szikra Tamas,Papasaikas Panagiotis,Cuttat Rachel,Waldt Annick,Diggelmann Roland,Patino-Alvarez Claudia P.,Gerber-Hollbach Nadine,Schuierer Sven,Hou Yanyan,Srdanovic Aldin,Balogh Marton,Panero Riccardo,Hasler Pascal W.,Kusnyerik Akos,Szabo Arnold,Stadler Michael B.,Orgül Selim,Hierlemann Andreas,Scholl Hendrik P. N.,Roma Guglielmo,Nigsch Florian,Roska Botond
Abstract
SummaryHow closely human organoids recapitulate cell-type diversity and cell-type maturation of their target organs is not well understood. We developed human retinal organoids with multiple nuclear and synaptic layers. We sequenced the RNA of 158,844 single cells from these organoids at six 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 and the transcriptomes of organoid cell types converged towards the transcriptomes of adult peripheral retinal cell types. The expression of disease-associated genes was significantly 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 adult human retinas.
Publisher
Cold Spring Harbor Laboratory
Cited by
16 articles.
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