FRS2α regulates Erk levels to control a self-renewal target Hes1 and proliferation of FGF-responsive neural stem/progenitor cells

Takuya Sato, Takuya Shimazaki, Hayato Naka, Shin Ichi Fukami, Yasushi Satoh, Hideyuki Okano, Lax Irit, Joseph Schlessinger, Noriko Gotoh

研究成果: Article査読

25 被引用数 (Scopus)

抄録

Fibroblast growth factor (FGF) is among the most common growth factors used in cultures to maintain self-renewal and proliferative capabilities of a variety of stem cells, including neural stem cells (NSCs). However, the molecular mechanisms underlying the control by FGF have remained elusive. Studies on mutant mice of FGF receptor substrate 2α (FRS2α), a central mediator for FGF signaling, combined with FRS2α knockdown or gain-of-function experiments, allowed us to dissect the role of FGF signaling for the self-renewal and proliferation of NSCs and to provide novel molecular mechanisms for them. We identified Hes1 as a novel self-renewal target of FGF-signaling. Quantitatively different levels of Erk activation mediated by FRS2α may regulate self-renewal of NSCs and proliferation of neural stem/progenitor cells (NSPCs); low levels of Erk activation are sufficient for the former, however, higher levels are required for maximum activity of the latter. Thus, FRS2α fine-tunes the FGF-signaling to control qualitatively different biological activities, self-renewal at least partly through Hes1 versus proliferation of NSPCs.

本文言語English
ページ(範囲)1661-1673
ページ数13
ジャーナルStem Cells
28
9
DOI
出版ステータスPublished - 2010 9

ASJC Scopus subject areas

  • 分子医療
  • 発生生物学
  • 細胞生物学

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