NF-κB and TNF Affect the Astrocytic Differentiation from Neural Stem Cells

Cells. 2021 Apr 8;10(4):840. doi: 10.3390/cells10040840.

Abstract

The NF-κB signaling pathway is crucial during development and inflammatory processes. We have previously shown that NF-κB activation induces dedifferentiation of astrocytes into neural progenitor cells (NPCs). Here, we provide evidence  that the NF-κB pathway plays also a fundamental role during the differentiation of NPCs into astrocytes. First, we show that the NF-κB pathway is essential to initiate astrocytic differentiation as its early inhibition induces NPC apoptosis and impedes their differentiation. Second, we demonstrate that persistent NF-κB activation affects NPC-derived astrocyte differentiation. Tumor necrosis factor (TNF)-treated NPCs show NF-κB activation, maintain their multipotential and proliferation properties, display persistent expression of immature markers and inhibit astrocyte markers. Third, we analyze the effect of  NF-κB activation on the main known astrocytic differentiation pathways, such as NOTCH and JAK-STAT. Our findings suggest that the NF-κB pathway plays a dual fundamental role during NPC differentiation into astrocytes: it promotes astrocyte specification, but its persistent activation impedes their differentiation.

Keywords: NF-κB; apoptosis; astrocyte; differentiation; neural progenitor cell; tumor necrosis factor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Astrocytes / cytology*
  • Astrocytes / metabolism*
  • Biomarkers / metabolism
  • Cell Differentiation*
  • Cell Proliferation
  • Glial Fibrillary Acidic Protein / metabolism
  • Janus Kinases / metabolism
  • Mice
  • Mice, Inbred C57BL
  • Multipotent Stem Cells / metabolism
  • NF-kappa B / metabolism*
  • Neural Stem Cells / cytology*
  • Phenotype
  • Receptors, Notch / metabolism
  • STAT Transcription Factors / metabolism
  • Signal Transduction
  • Tumor Necrosis Factor-alpha / metabolism*

Substances

  • Biomarkers
  • Glial Fibrillary Acidic Protein
  • NF-kappa B
  • Receptors, Notch
  • STAT Transcription Factors
  • Tumor Necrosis Factor-alpha
  • Janus Kinases