Human cerebral organoids recapitulate gene expression programs of fetal neocortex development

J. Gray Camp(Max Planck Institute for Evolutionary Anthropology), Farhath Badsha(Max Planck Institute of Molecular Cell Biology and Genetics), Marta Florio(Max Planck Institute of Molecular Cell Biology and Genetics), Sabina Kanton(Max Planck Institute for Evolutionary Anthropology), Tobias Gerber(Max Planck Institute for Evolutionary Anthropology), Michaela Wilsch‐Bräuninger(Max Planck Institute of Molecular Cell Biology and Genetics), Éric Lewitus(Institut de Biologie de l'École Normale Supérieure), Alex M. Sykes(Max Planck Institute of Molecular Cell Biology and Genetics), Wulf Hevers(Max Planck Institute for Evolutionary Anthropology), Madeline A. Lancaster(Institute of Molecular Biotechnology), Juergen A. Knoblich(Institute of Molecular Biotechnology), Robert Lachmann(Klinik für Frauenheilkunde), Svante Pääbo(Max Planck Institute for Evolutionary Anthropology), Wieland Β. Huttner(Max Planck Institute of Molecular Cell Biology and Genetics), Barbara Treutlein(Max Planck Institute for Evolutionary Anthropology)
Proceedings of the National Academy of Sciences
December 7, 2015
Cited by 1,164

Abstract

Cerebral organoids-3D cultures of human cerebral tissue derived from pluripotent stem cells-have emerged as models of human cortical development. However, the extent to which in vitro organoid systems recapitulate neural progenitor cell proliferation and neuronal differentiation programs observed in vivo remains unclear. Here we use single-cell RNA sequencing (scRNA-seq) to dissect and compare cell composition and progenitor-to-neuron lineage relationships in human cerebral organoids and fetal neocortex. Covariation network analysis using the fetal neocortex data reveals known and previously unidentified interactions among genes central to neural progenitor proliferation and neuronal differentiation. In the organoid, we detect diverse progenitors and differentiated cell types of neuronal and mesenchymal lineages and identify cells that derived from regions resembling the fetal neocortex. We find that these organoid cortical cells use gene expression programs remarkably similar to those of the fetal tissue to organize into cerebral cortex-like regions. Our comparison of in vivo and in vitro cortical single-cell transcriptomes illuminates the genetic features underlying human cortical development that can be studied in organoid cultures.


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