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Molecular logic of cellular diversification in the mouse cerebral cortex.
Di Bella, Daniela J; Habibi, Ehsan; Stickels, Robert R; Scalia, Gabriele; Brown, Juliana; Yadollahpour, Payman; Yang, Sung Min; Abbate, Catherine; Biancalani, Tommaso; Macosko, Evan Z; Chen, Fei; Regev, Aviv; Arlotta, Paola.
Afiliação
  • Di Bella DJ; Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, USA.
  • Habibi E; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Stickels RR; Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, USA.
  • Scalia G; Klarman Cell Observatory, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Brown J; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Yadollahpour P; Klarman Cell Observatory, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Yang SM; Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, USA.
  • Abbate C; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Biancalani T; Klarman Cell Observatory, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Macosko EZ; Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, USA.
  • Chen F; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
  • Regev A; Department of Stem Cell and Regenerative Biology, Harvard University, Cambridge, MA, USA.
  • Arlotta P; Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Nature ; 595(7868): 554-559, 2021 07.
Article em En | MEDLINE | ID: mdl-34163074
ABSTRACT
The mammalian cerebral cortex has an unparalleled diversity of cell types, which are generated during development through a series of temporally orchestrated events that are under tight evolutionary constraint and are critical for proper cortical assembly and function1,2. However, the molecular logic that governs the establishment and organization of cortical cell types remains unknown, largely due to the large number of cell classes that undergo dynamic cell-state transitions over extended developmental timelines. Here we generate a comprehensive atlas of the developing mouse neocortex, using single-cell RNA sequencing and single-cell assay for transposase-accessible chromatin using sequencing. We sampled the neocortex every day throughout embryonic corticogenesis and at early postnatal ages, and complemented the sequencing data with a spatial transcriptomics time course. We computationally reconstruct developmental trajectories across the diversity of cortical cell classes, and infer their spatial organization and the gene regulatory programs that accompany their lineage bifurcation decisions and differentiation trajectories. Finally, we demonstrate how this developmental map pinpoints the origin of lineage-specific developmental abnormalities that are linked to aberrant corticogenesis in mutant mice. The data provide a global picture of the regulatory mechanisms that govern cellular diversification in the neocortex.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neocórtex / Neurogênese Limite: Animals Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neocórtex / Neurogênese Limite: Animals Idioma: En Ano de publicação: 2021 Tipo de documento: Article