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A small molecule accelerates neuronal differentiation in the adult rat

Authors
Wurdak, H.Zhu, S.Min, K.H.Aimone, L.Lairson, L.L.Watson, J.Chopiuk, G.Demas, J.Charette, B.Weerapana, E.Cravatt, B.F.Cline, H.T.Peters, E.C.Zhang, J.Walker, J.R.Wu, C.Chang, J.Tuntland, T.Cho, C.Y.Schultz, P.G.
Issue Date
Sep-2010
Publisher
NATL ACAD SCIENCES, 2101 CONSTITUTION AVE NW, WASHINGTON, DC 20418 USA
Keywords
Adult neurogenesis; Neural progenitor cell; Tacc3
Citation
Proceedings of the National Academy of Sciences of the United States of America, v.107, no.38, pp 16542 - 16547
Pages
6
Journal Title
Proceedings of the National Academy of Sciences of the United States of America
Volume
107
Number
38
Start Page
16542
End Page
16547
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/22752
DOI
10.1073/pnas.1010300107
ISSN
0027-8424
1091-6490
Abstract
Adult neurogenesis occurs in mammals and provides a mechanism for continuous neural plasticity in the brain. However, little is known about the molecular mechanisms regulating hippocampal neural progenitor cells (NPCs) and whether their fate can be pharmacologically modulated to improve neural plasticity and regeneration. Here, we report the characterization of a small molecule (KHS101) that selectively induces a neuronal differentiation phenotype. Mechanism of action studies revealed a link of KHS101 to cell cycle exit and specific binding to the TACC3 protein, whose knockdown in NPCs recapitulates the KHS101-induced phenotype. Upon systemic administration, KHS101 distributed to the brain and resulted in a significant increase in neuronal differentiation in vivo. Our findings indicate that KHS101 accelerates neuronal differentiation by interaction with TACC3 and may provide a basis for pharmacological intervention directed at endogenous NPCs.
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Min, Kyung Hoon
대학원 (글로벌혁신신약학과)
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