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Genetic recovery of ErbB4 in adulthood partially restores brain functions in null mice.


ABSTRACT: Neurotrophic factor NRG1 and its receptor ErbB4 play a role in GABAergic circuit assembly during development. ErbB4 null mice possess fewer interneurons, have decreased GABA release, and show impaired behavior in various paradigms. In addition, NRG1 and ErbB4 have also been implicated in regulating GABAergic transmission and plasticity in matured brains. However, current ErbB4 mutant strains are unable to determine whether phenotypes in adult mutant mice result from abnormal neural development. This important question, a glaring gap in understanding NRG1-ErbB4 function, was addressed by using two strains of mice with temporal control of ErbB4 deletion and expression, respectively. We found that ErbB4 deletion in adult mice impaired behavior and GABA release but had no effect on neuron numbers and morphology. On the other hand, some deficits due to the ErbB4 null mutation during development were alleviated by restoring ErbB4 expression at the adult stage. Together, our results indicate a critical role of NRG1-ErbB4 signaling in GABAergic transmission and behavior in adulthood and suggest that restoring NRG1-ErbB4 signaling at the postdevelopmental stage might benefit relevant brain disorders.

SUBMITTER: Wang H 

PROVIDER: S-EPMC6304932 | biostudies-literature | 2018 Dec

REPOSITORIES: biostudies-literature

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Genetic recovery of ErbB4 in adulthood partially restores brain functions in null mice.

Wang Hongsheng H   Liu Fang F   Chen Wenbing W   Sun Xiangdong X   Cui Wanpeng W   Dong Zhaoqi Z   Zhao Kai K   Zhang Hongsheng H   Li Haiwen H   Xing Guanglin G   Fei Erkang E   Pan Bing-Xing BX   Li Bao-Ming BM   Xiong Wen-Cheng WC   Mei Lin L  

Proceedings of the National Academy of Sciences of the United States of America 20181129 51


Neurotrophic factor NRG1 and its receptor ErbB4 play a role in GABAergic circuit assembly during development. ErbB4 null mice possess fewer interneurons, have decreased GABA release, and show impaired behavior in various paradigms. In addition, NRG1 and ErbB4 have also been implicated in regulating GABAergic transmission and plasticity in matured brains. However, current ErbB4 mutant strains are unable to determine whether phenotypes in adult mutant mice result from abnormal neural development.  ...[more]

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