DNA damage in mammalian neural stem cells leads to astrocytic differentiation mediated by BMP2 signaling through JAK-STAT

Stem Cell Reports. 2013 Jul 25;1(2):123-38. doi: 10.1016/j.stemcr.2013.06.004. eCollection 2013.


The consequences of DNA damage generation in mammalian somatic stem cells, including neural stem cells (NSCs), are poorly understood despite their potential relevance for tissue homeostasis. Here, we show that, following ionizing radiation-induced DNA damage, NSCs enter irreversible proliferative arrest with features of cellular senescence. This is characterized by increased cytokine secretion, loss of stem cell markers, and astrocytic differentiation. We demonstrate that BMP2 is necessary to induce expression of the astrocyte marker GFAP in irradiated NSCs via a noncanonical signaling pathway engaging JAK-STAT. This is promoted by ATM and antagonized by p53. Using a SOX2-Cre reporter mouse model for cell-lineage tracing, we demonstrate irradiation-induced NSC differentiation in vivo. Furthermore, glioblastoma assays reveal that irradiation therapy affects the tumorigenic potential of cancer stem cells by ablating self-renewal and inducing astroglial differentiation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Astrocytes / metabolism*
  • Bone Morphogenetic Protein 2 / metabolism*
  • Cell Differentiation* / radiation effects
  • Cell Proliferation / radiation effects
  • DNA Damage
  • Glioblastoma / radiotherapy*
  • Humans
  • Mice
  • Mice, Inbred C57BL
  • Neoplastic Stem Cells / radiation effects
  • Neural Stem Cells / radiation effects*
  • SOXB1 Transcription Factors / metabolism
  • Signal Transduction* / radiation effects


  • Bone Morphogenetic Protein 2
  • SOXB1 Transcription Factors

Associated data

  • GEO/GSE38031