Disrupted-in-schizophrenia 1 regulates integration of newly generated neurons in the adult brain

被引:485
作者
Duan, Xin
Chang, Jay H.
Ge, Shaoyu
Faulkner, Regina L.
Kim, Ju Young
Kitabatake, Yasuji
Liu, Xiao-bo
Yang, Chih-Hao
Jordan, J. Dedrick
Ma, Dengke K.
Liu, Cindy Y.
Ganesan, Sundar
Cheng, Hwai-Jong
Ming, Guo-li
Lu, Bai
Song, Hongjun
机构
[1] Johns Hopkins Univ, Sch Med, Inst Cell Engn, Baltimore, MD 21205 USA
[2] Johns Hopkins Univ, Sch Med, Solomon H Snyder Dept Neurosci, Baltimore, MD 21205 USA
[3] NIMH, Genes Cognit & Psychosis Program, NIH, Bethesda, MD 20892 USA
[4] Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21205 USA
[5] Univ Calif Davis, Ctr Neurosci, Davis, CA 95616 USA
[6] NICHHD, Sect Neural Dev, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1016/j.cell.2007.07.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Adult neurogenesis occurs throughout life in discrete regions of the adultmammalian brain. Little is known about the mechanism governing the sequential developmental process that leads to integration of new neurons from adult neural stem cells into the existing circuitry. Here, we investigated roles of Disrupted- In- Schizophrenia 1 ( DISC1), a schizophrenia susceptibility gene, in adult hippocampal neurogenesis. Unexpectedly, downregulation of DISC1 leads to accelerated neuronal integration, resulting in aberrant morphological development and mispositioning of new dentate granule cells in a cell- autonomous fashion. Functionally, newborn neurons with DISC1 knockdown exhibit enhanced excitability and accelerated dendritic development and synapse formation. Furthermore, DISC1 cooperates with its binding partner NDEL1 in regulating adult neurogenesis. Taken together, our study identifies DISC1 as a key regulator that orchestrates the tempo of functional neuronal integration in the adult brain and demonstrates essential roles of a susceptibility gene for major mental illness in neuronal development, including adult neurogenesis.
引用
收藏
页码:1146 / 1158
页数:13
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