Abstract

SummaryHuman 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.

Highlights

  • Human organoids are 3D cellular ensembles that are grown in vitro from adult or pluripotent stem cells and reproduce some morphological, functional, and transcriptomic features of human organs (Clevers, 2016; Lancaster and Knoblich, 2014a)

  • We provide a comparative atlas of cell-type transcriptomes of human retinal organoid and healthy adult human retina that allows identification of cellular targets for studying disease mechanisms in organoids and targeted repair in adult human retinas

  • Multilayered Human Retinal Organoids in Quantity We aimed to develop human retinal organoids with three nuclear and two synaptic layers from induced pluripotent stem cells (iPSCs), building on the observation that iPSC lines vary in their potential to produce retinal organoids: some gave rise to organoids while others did not

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Summary

Introduction

Human organoids are 3D cellular ensembles that are grown in vitro from adult or pluripotent stem cells and reproduce some morphological, functional, and transcriptomic features of human organs (Clevers, 2016; Lancaster and Knoblich, 2014a). With few exceptions (Camp et al, 2017; Subramanian et al, 2019), it is not well understood how the transcriptomes of cell types in organoids converge toward the cell type transcriptomes of the adult organ. Nor is it well understood which disease genes retain their specificity for cell types between the target organ and its organoids or to what extent the function of cell types and their circuits are retained in organoids. How organoids are employed as a model system of diseases in adults will be guided by the answers to these questions

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