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Cholinergic Circuit Control of Postnatal Neurogenesis.
Asrican, Brent; Paez-Gonzalez, Patricia; Erb, Joshua; Kuo, Chay T.
Afiliación
  • Asrican B; Department of Cell Biology, Duke University School of Medicine, Durham, NC 27710, USA.
  • Paez-Gonzalez P; Department of Cell Biology, Duke University School of Medicine, Durham, NC 27710, USA.
  • Erb J; Department of Cell Biology, Duke University School of Medicine, Durham, NC 27710, USA; Neurobiology Graduate Training Program, Duke University School of Medicine, Durham, NC 27710, USA.
  • Kuo CT; Department of Cell Biology, Duke University School of Medicine, Durham, NC 27710, USA; Neurobiology Graduate Training Program, Duke University School of Medicine, Durham, NC 27710, USA; Brumley Neonatal Perinatal Research Institute, Duke University School of Medicine, Durham, NC 27710, USA; Departme
Article en En | MEDLINE | ID: mdl-27468423
ABSTRACT
New neuron addition via continued neurogenesis in the postnatal/adult mammalian brain presents a distinct form of nervous system plasticity. During embryonic development, precise temporal and spatial patterns of neurogenesis are necessary to create the nervous system architecture. Similar between embryonic and postnatal stages, neurogenic proliferation is regulated by neural stem cell (NSC)-intrinsic mechanisms layered upon cues from their local microenvironmental niche. Following developmental assembly, it remains relatively unclear what may be the key driving forces that sustain continued production of neurons in the postnatal/adult brain. Recent experimental evidence suggests that patterned activity from specific neural circuits can also directly govern postnatal/adult neurogenesis. Here, we review experimental findings that revealed cholinergic modulation, and how patterns of neuronal activity and acetylcholine release may differentially or synergistically activate downstream signaling in NSCs. Higher-order excitatory and inhibitory inputs regulating cholinergic neuron firing, and their implications in neurogenesis control are also considered.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Neurogenesis (Austin) Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Neurogenesis (Austin) Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos
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