Non-canonical Wnt signaling regulates neural stem cell quiescence during homeostasis and after demyelination

被引:67
作者
Chavali, Manideep [1 ,2 ,4 ]
Klingener, Michael [1 ]
Kokkosis, Alexandros G. [1 ]
Garkun, Yury [3 ]
Felong, Sylwia [1 ]
Maffei, Arianna [3 ]
Aguirre, Adan [1 ]
机构
[1] SUNY Stony Brook, Dept Pharmacol Sci, Stony Brook, NY 11794 USA
[2] SUNY Stony Brook, Mat Sci & Engn, Stony Brook, NY 11794 USA
[3] SUNY Stony Brook, Dept Neurobiol & Behav, Stony Brook, NY 11794 USA
[4] Univ Calif San Francisco, Eli & Edythe Broad, Ctr Regenerat Med & Stem Cell, San Francisco, CA 94143 USA
关键词
ADULT SUBEPENDYMAL ZONE; SUBVENTRICULAR ZONE; VASCULAR NICHE; PROGENITOR CELLS; SHOTGUN PROTEOMICS; EMBRYONIC ORIGIN; ANALYSES REVEAL; APICAL SURFACE; CHOROID-PLEXUS; SELF-RENEWAL;
D O I
10.1038/s41467-017-02440-0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Adult neural stem cells (NSCs) reside in a specialized microenvironment, the subventricular zone (SVZ), which provides them with unique signaling cues to control their basic properties and prevent their exhaustion. While the signaling mechanisms that regulate NSC lineage progression are well characterized, the molecular mechanisms that trigger the activation of quiescent NSCs during homeostasis and tissue repair are still unclear. Here, we uncovered that the NSC quiescent state is maintained by Rho-GTPase Cdc42, a downstream target of non-canonical Wnt signaling. Mechanistically, activation of Cdc42 induces expression of molecules involved in stem cell identity and anchorage to the niche. Strikingly, during a demyelination injury, downregulation of non-canonical Wnt-dependent Cdc42 activity is necessary to promote activation and lineage progression of quiescent NSCs, thereby initiating the process of tissue repair.
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页数:17
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