Control of Adult Neurogenesis by Short-Range Morphogenic-Signaling Molecules

被引:45
作者
Choe, Youngshik [1 ,2 ,3 ]
Pleasure, Samuel J. [1 ,2 ,3 ]
Mira, Helena [4 ]
机构
[1] UCSF Inst Regenerat Med, Dept Neurol, Program Neurosci Biol, San Francisco, CA 94158 USA
[2] UCSF Inst Regenerat Med, Dept Neurol, Program Dev Biol, San Francisco, CA 94158 USA
[3] UCSF Inst Regenerat Med, Dept Neurol, Program Stem Cell Biol, San Francisco, CA 94158 USA
[4] Inst Salud Carlos III, UFIEC, Chron Dis Programme, Madrid 28220, Spain
关键词
NEURAL STEM-CELLS; CENTRAL-NERVOUS-SYSTEM; POSTNATAL DENTATE GYRUS; NUCLEAR RECEPTOR TLX; SONIC-HEDGEHOG; HIPPOCAMPAL NEUROGENESIS; PROGENITOR CELLS; IN-VIVO; SUBVENTRICULAR ZONE; SELF-RENEWAL;
D O I
10.1101/cshperspect.a018887
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Adult neurogenesis is dynamically regulated by a tangled web of local signals emanating from the neural stem cell (NSC) microenvironment. Both soluble and membrane-bound niche factors have been identified as determinants of adult neurogenesis, including morphogens. Here, we review our current understanding of the role and mechanisms of short-range morphogen ligands from the Wnt, Notch, Sonic hedgehog, and bone morphogenetic protein (BMP) families in the regulation of adult neurogenesis. These morphogens are ideally suited to fine-tune stem-cell behavior, progenitor expansion, and differentiation, thereby influencing all stages of the neurogenesis process. We discuss cross talk between their signaling pathways and highlight findings of embryonic development that provide a relevant context for understanding neurogenesis in the adult brain. We also review emerging examples showing that the web of morphogens is in fact tightly linked to the regulation of neurogenesis by diverse physiologic processes.
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页数:18
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