Distinct progenitor behavior underlying neocortical gliogenesis related to tumorigenesis.

Cell Rep

IDG/McGovern Institute for Brain Research, Tsinghua-Peking Center for Life Sciences, Beijing Frontier Research Center of Biological Structure, Beijing Advanced Innovation Center for Structural Biology, School of Life Sciences, Tsinghua University, Beijing 100084, China; Neuroscience Graduate Program, Feil Family Brain & Mind Research Institute, Weill Cornell Medical College, New York, NY 10065, USA. Electronic address:

Published: March 2021

AI Article Synopsis

  • Radial glial progenitors (RGPs) are crucial for producing most neurons and glial cells in the neocortex, but the process of gliogenesis (formation of glial cells) is not fully understood.
  • This study reveals that RGPs transition from generating neurons to glial cells and produce astrocytes and oligodendrocytes in specific proportions (about 60%, 15%, and 25%, respectively) through intermediate precursor cells (IPCs).
  • Clonal loss of the Neurofibromatosis type 1 tumor suppressor results in excess glial production, particularly oligodendrocyte precursor cells, highlighting the cellular mechanisms of gliogenesis and potential links to brain

Article Abstract

Radial glial progenitors (RGPs) give rise to the vast majority of neurons and glia in the neocortex. Although RGP behavior and progressive generation of neocortical neurons have been delineated, the exact process of neocortical gliogenesis remains elusive. Here, we report the precise progenitor behavior and gliogenesis program at single-cell resolution in the mouse neocortex. Fractions of dorsal RGPs transition from neurogenesis to gliogenesis progressively, producing astrocytes, oligodendrocytes, or both in well-defined propensities of ∼60%, 15%, and 25%, respectively, by fate-restricted "intermediate" precursor cells (IPCs). Although the total number of IPCs generated by individual RGPs appears stochastic, the output of individual IPCs exhibit clear patterns in number and subtype and form discrete local subclusters. Clonal loss of tumor suppressor Neurofibromatosis type 1 leads to excessive production of glia selectively, especially oligodendrocyte precursor cells. These results quantitatively delineate the cellular program of neocortical gliogenesis and suggest the cellular and lineage origin of primary brain tumor.

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Source
http://dx.doi.org/10.1016/j.celrep.2021.108853DOI Listing

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