Overproduction of Upper-Layer Neurons in the Neocortex Leads to Autism-like Features in Mice

被引:101
作者
Fang, Wei-Qun [1 ]
Chen, Wei-Wei [1 ]
Jiang, Liwen [2 ,3 ]
Liu, Kai [1 ]
Yung, Wing-Ho [4 ]
Fu, Amy K. Y. [1 ]
Ip, Nancy Y. [1 ]
机构
[1] Hong Kong Univ Sci & Technol, Mol Neurosci Ctr, Ctr Stem Cell Res, Div Life Sci,State Key Lab Mol Neurosci, Hong Kong, Hong Kong, Peoples R China
[2] Chinese Univ Hong Kong, Ctr Cell & Dev Biol, Sch Life Sci, Shatin, Hong Kong, Peoples R China
[3] Chinese Univ Hong Kong, State Key Lab Agrobiotechnol, Shatin, Hong Kong, Peoples R China
[4] Chinese Univ Hong Kong, Sch Biomed Sci, Shatin, Hong Kong, Peoples R China
关键词
CEREBRAL-CORTEX; NERVOUS-SYSTEM; MOUSE MODELS; AXIN DIRECTS; MECHANISMS;
D O I
10.1016/j.celrep.2014.11.003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The functional integrity of the neocortex depends upon proper numbers of excitatory and inhibitory neurons; however, the consequences of dysregulated neuronal production during the development of the neocortex are unclear. As excess cortical neurons are linked to the neurodevelopmental disorder autism, we investigated whether the overproduction of neurons leads to neocortical malformation and malfunction in mice. We experimentally increased the number of pyramidal neurons in the upper neocortical layers by using the small molecule XAV939 to expand the intermediate progenitor population. The resultant overpopulation of neurons perturbs development of dendrites and spines of excitatory neurons and alters the laminar distribution of interneurons. Furthermore, these phenotypic changes are accompanied by dysregulated excitatory and inhibitory synaptic connection and balance. Importantly, these mice exhibit behavioral abnormalities resembling those of human autism. Thus, our findings collectively suggest a causal relationship between neuronal overproduction and autism-like features, providing developmental insights into the etiology of autism.
引用
收藏
页码:1635 / 1643
页数:9
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