Dominant-negative DISC1 transgenic mice display schizophrenia-associated phenotypes detected by measures translatable to humans

被引:310
作者
Hikida, Takatoshi
Jaaro-Peled, Hanna
Seshadri, Saurav
Oishi, Kenichi
Hookway, Caroline
Kong, Stephanie
Wu, Di
Xue, Rong
Andrade, Manuella
Tankou, Stephanie
Mori, Susumu
Gallagher, Michela
Ishizuka, Koko
Pletnikov, Mikhail
Kida, Satoshi
Sawa, Akira [1 ]
机构
[1] Johns Hopkins Univ Hosp, Grad Program Cellular & Mol Med, Baltimore, MD 21287 USA
[2] Johns Hopkins Univ Hosp, Dept Psychiat & Behav Sci, Baltimore, MD 21287 USA
[3] Johns Hopkins Univ Hosp, Dept Radiol, Baltimore, MD 21287 USA
[4] Johns Hopkins Univ Hosp, Dept Neurosci, Baltimore, MD 21287 USA
[5] Johns Hopkins Univ Hosp, Dept Psychol, Baltimore, MD 21287 USA
[6] Johns Hopkins Univ Hosp, Div Neurobiol, Baltimore, MD 21287 USA
[7] Tokyo Univ Agr, Fac Appl Biosci, Dept Biosci, Tokyo 1568502, Japan
关键词
D O I
10.1073/pnas.0704774104
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
Here, we report generation and characterization of Disrupted-In-Schizophrenia-1 (DISC1) genetically engineered mice as a potential model for major mental illnesses, such as schizophrenia. DISC1 is a promising genetic risk factor for major mental illnesses. In this transgenic model, a dominant-negative form of DISC1 (DN-DISC1) is expressed under the alpha CaMKII promoter. in vivo MRI of the DN-DISC1 mice detected enlarged lateral ventricles particularly on the left side, suggesting a link to the asymmetrical change in anatomy found in brains of patients with schizophrenia. Furthermore, selective reduction in the immunoreactivity of parvalbumin in the cortex, a marker for an interneuron deficit that may underlie cortical asynchrony, is observed in the DN-DISC1 mice. These results suggest that these transgenic mice may be used as a model for schizophrenia. DN-DISC1 mice also display several behavioral abnormalities, including hyperactivity, disturbance in sensorimotor gating and olfactory-associated behavior, and an anhedonia/depression-like deficit.
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收藏
页码:14501 / 14506
页数:6
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