Adult neural stem cells and their niche: a dynamic duo during homeostasis, regeneration, and aging

V Silva-Vargas, EE Crouch, F Doetsch - Current opinion in neurobiology, 2013 - Elsevier
V Silva-Vargas, EE Crouch, F Doetsch
Current opinion in neurobiology, 2013Elsevier
Highlights•Stem cells span different compartments of the niche and integrate both local and
long-range signals.•Anchorage to the niche, biophysical properties of the niche, such as
CSF flow, and circuitry are emerging as important regulators of stem cell quiescence.•Neural
stem cells and their progeny interact reciprocally with each other and with their niche.•The
niche changes under different physiological states, including aging, affecting neural stem
cell proliferation and neurogenesis.Stem cells persist in specialized niches in the adult …
Highlights
  • Stem cells span different compartments of the niche and integrate both local and long-range signals.
  • Anchorage to the niche, biophysical properties of the niche, such as CSF flow, and circuitry are emerging as important regulators of stem cell quiescence.
  • Neural stem cells and their progeny interact reciprocally with each other and with their niche.
  • The niche changes under different physiological states, including aging, affecting neural stem cell proliferation and neurogenesis.
Stem cells persist in specialized niches in the adult mammalian brain. Emerging findings highlight the complexity and heterogeneity of different compartments in the niche, as well as the presence of local signaling microdomains. Stem cell quiescence and activation are regulated not only by anchorage to the niche and diffusible signals, but also by biophysical properties, including fluid dynamics. Importantly, the adult neural stem cell niche integrates both local and systemic changes, reflecting the physiological state of the organism. Moreover niche signaling is bidirectional, with stem cells and their progeny and niche cells dynamically interacting with each other during homeostasis, regeneration and aging.
Elsevier