A comparative transcriptomic analysis of astrocytes differentiation from human neural progenitor cells.

Journal Article (Journal Article)

Astrocytes are a morphologically and functionally heterogeneous population of cells that play critical roles in neurodevelopment and in the regulation of central nervous system homeostasis. Studies of human astrocytes have been hampered by the lack of specific molecular markers and by the difficulties associated with purifying and culturing astrocytes from adult human brains. Human neural progenitor cells (NPCs) with self-renewal and multipotent properties represent an appealing model system to gain insight into the developmental genetics and function of human astrocytes, but a comprehensive molecular characterization that confirms the validity of this cellular system is still missing. Here we used an unbiased transcriptomic analysis to characterize in vitro culture of human NPCs and to define the gene expression programs activated during the differentiation of these cells into astrocytes using FBS or the combination of CNTF and BMP4. Our results demonstrate that in vitro cultures of human NPCs isolated during the gliogenic phase of neurodevelopment mainly consist of radial glial cells (RGCs) and glia-restricted progenitor cells. In these cells the combination of CNTF and BMP4 activates the JAK/STAT and SMAD signaling cascades, leading to the inhibition of oligodendrocytes lineage commitment and activation of astrocytes differentiation. On the other hand, FBS-derived astrocytes have properties of reactive astrocytes. Our work suggests that in vitro culture of human NPCs represents a valuable cellular system to study human disorders characterized by impairment of astrocytes development and function. Our datasets represent an important resource for researchers studying human astrocytes development and might set the basis for the discovery of novel human-specific astrocyte markers.

Full Text

Duke Authors

Cited Authors

  • Magistri, M; Khoury, N; Mazza, EMC; Velmeshev, D; Lee, JK; Bicciato, S; Tsoulfas, P; Faghihi, MA

Published Date

  • November 2016

Published In

Volume / Issue

  • 44 / 10

Start / End Page

  • 2858 - 2870

PubMed ID

  • 27564458

Pubmed Central ID

  • PMC5118072

Electronic International Standard Serial Number (EISSN)

  • 1460-9568

Digital Object Identifier (DOI)

  • 10.1111/ejn.13382


  • eng

Conference Location

  • France