Disrupted in Schizophrenia 1 Regulates Neuronal Progenitor Proliferation via Modulation of GSK3β/β-Catenin Signaling

被引:653
作者
Mao, Yingwei [1 ,2 ,3 ]
Ge, Xuecai [1 ,2 ]
Frank, Christopher L. [1 ,2 ]
Madison, Jon M. [8 ,9 ]
Koehler, Angela N. [6 ,7 ]
Doud, Mary Kathryn [6 ,7 ]
Tassa, Carlos [6 ,7 ]
Berry, Erin M. [6 ,7 ,8 ,9 ]
Soda, Takahiro [1 ,2 ,4 ,5 ]
Singh, Karun K. [1 ,2 ]
Biechele, Travis [1 ,10 ,11 ]
Petryshen, Tracey L. [6 ,7 ,8 ,9 ]
Moon, Randall T. [1 ,10 ,11 ]
Haggarty, Stephen J. [6 ,7 ,8 ,9 ]
Tsai, Li-Huei [1 ,2 ,8 ,9 ]
机构
[1] MIT, Howard Hughes Med Inst, Cambridge, MA 02139 USA
[2] MIT, Picower Inst Learning & Memory, Dept Brain & Cognit Sci, Cambridge, MA 02139 USA
[3] Harvard Univ, Sch Med, Program Neurosci, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Phd Program, Boston, MA 02115 USA
[5] MIT, Harvard Mit Div Hlth Sci & Technol, Cambridge, MA 02139 USA
[6] Massachusetts Gen Hosp, Psychiat & Neurodev Genet Unit, Ctr Human Genet Res, Boston, MA 02114 USA
[7] Massachusetts Gen Hosp, Mol Neurogenet Unit, Ctr Human Genet Res, Boston, MA 02114 USA
[8] Broad Inst Harvard, Stanley Ctr Psychiat Res, Cambridge, MA 02139 USA
[9] MIT, Cambridge, MA 02139 USA
[10] Univ Washington, Dept Pharmacol, Seattle, WA 98195 USA
[11] Univ Washington, Inst Stem Cell & Regenerat Med, Seattle, WA 98195 USA
基金
美国国家卫生研究院; 加拿大自然科学与工程研究理事会;
关键词
GLYCOGEN-SYNTHASE KINASE-3; BETA-CATENIN; HIPPOCAMPAL NEUROGENESIS; DISC1; BRAIN; MICE; LITHIUM; CELLS; DISRUPTED-IN-SCHIZOPHRENIA-1; EXPRESSION;
D O I
10.1016/j.cell.2008.12.044
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
The Disrupted in Schizophrenia 1 (DISC1) gene is disrupted by a balanced chromosomal translocation (1; 11) (q42; q14.3) in a Scottish family with a high incidence of major depression, schizophrenia, and bipolar disorder. Subsequent studies provided indications that DISC1 plays a role in brain development. Here, we demonstrate that suppression of DISC1 expression reduces neural progenitor proliferation, leading to premature cell cycle exit and differentiation. Several lines of evidence suggest that DISC1 mediates this function by regulating GSK3 beta. First, DISC1 inhibits GSK3 beta activity through direct physical interaction, which reduces beta-catenin phosphorylation and stabilizes beta-catenin. Importantly, expression of stabilized beta-catenin overrides the impairment of progenitor proliferation caused by DISC1 loss of function. Furthermore, GSK3 inhibitors normalize progenitor proliferation and behavioral defects caused by DISC1 loss of function. Together, these results implicate DISC1 inGSK3 beta/beta-catenin signaling pathways and provide a framework for understanding how alterations in this pathway may contribute to the etiology of psychiatric disorders.
引用
收藏
页码:1017 / 1031
页数:15
相关论文
共 46 条
[1]   beta-catenin is a target for the ubiquitin-proteasome pathway [J].
Aberle, H ;
Bauer, A ;
Stappert, J ;
Kispert, A ;
Kemler, R .
EMBO JOURNAL, 1997, 16 (13) :3797-3804
[2]   β-Catenin signaling promotes proliferation of progenitor cells in the adult mouse subventricular zone [J].
Adachi, Kazuhide ;
Mirzadeh, Zaman ;
Sakaguchi, Masanori ;
Yamashita, Toru ;
Nikolcheva, Tania ;
Gotoh, Yukiko ;
Peltz, Gary ;
Gong, Leyi ;
Kawase, Takeshi ;
Alvarez-Buylla, Arturo ;
Okano, Hideyuki ;
Sawamoto, Kazunobu .
STEM CELLS, 2007, 25 (11) :2827-2836
[3]  
Beaulieu JM, 2008, CELL, V132, P125, DOI 10.1016/j.cell.2007.11.041
[4]   Lithium antagonizes dopamine-dependent behaviors mediated by an AKT/glycogen synthase kinase 3 signaling cascade [J].
Beaulieu, JM ;
Sotnikova, TD ;
Yao, WD ;
Kockeritz, L ;
Woodgett, JR ;
Gainetdinov, RR ;
Caron, MG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (14) :5099-5104
[5]   An Akt/β-arrestin 2/PP2A signaling complex mediates dopaminergic neurotransmission and behavior [J].
Beaulieu, JM ;
Sotnikova, TD ;
Marion, S ;
Lefkowitz, RJ ;
Gainetdinov, RR ;
Caron, MG .
CELL, 2005, 122 (02) :261-273
[6]   Schizophrenia and affective disorders - Cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: Clinical and P300 findings in a family [J].
Blackwood, DHR ;
Fordyce, A ;
Walker, MT ;
St Clair, DM ;
Porteous, DJ ;
Muir, WJ .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (02) :428-433
[7]   Regulation of cerebral cortical size by control of cell cycle exit in neural precursors [J].
Chenn, A ;
Walsh, CA .
SCIENCE, 2002, 297 (5580) :365-369
[8]   The DISC locus in psychiatric illness [J].
Chubb, J. E. ;
Bradshaw, N. J. ;
Soares, D. C. ;
Porteous, D. J. ;
Millar, J. K. .
MOLECULAR PSYCHIATRY, 2008, 13 (01) :36-64
[9]   Behavioral phenotypes of Disc1 missense mutations in mice [J].
Clapcote, Steven J. ;
Lipina, Tatiana V. ;
Millar, J. Kirsty ;
Mackie, Shaun ;
Christie, Sheila ;
Ogawa, Fumiaki ;
Lerch, Jason P. ;
Trimble, Keith ;
Uchiyama, Masashi ;
Sakuraba, Yoshiyuki ;
Kaneda, Hideki ;
Shiroishi, Toshihiko ;
Houslay, Miles D. ;
Henkelman, R. Mark ;
Sled, John G. ;
Gondo, Yoichi ;
Porteous, David J. ;
Roder, John C. .
NEURON, 2007, 54 (03) :387-402
[10]   INHIBITION OF GLYCOGEN-SYNTHASE KINASE-3 BY INSULIN-MEDIATED BY PROTEIN-KINASE-B [J].
CROSS, DAE ;
ALESSI, DR ;
COHEN, P ;
ANDJELKOVICH, M ;
HEMMINGS, BA .
NATURE, 1995, 378 (6559) :785-789