Dysfunction of AMPA receptor GluA3 is associated with aggressive behavior in human

Shi Xiao Peng, Jingwen Pei, Berardo Rinaldi, Jiang Chen, Yu Han Ge, Min Jia, Jun Wang, Andrée Delahaye-Duriez, Jia Hui Sun, Yan Yu Zang, Yong Yun Shi, Ning Zhang, Xiang Gao, Donatella Milani, Xijia Xu, Nengyin Sheng, Benedicte Gerard, Chen Zhang, Allan Bayat, Na LiuJian Jun Yang, Yun Stone Shi*

*Kontaktforfatter

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Abstrakt

Inappropriate aggression in humans hurts the society, families and individuals. The genetic basis for aggressive behavior, however, remains largely elusive. In this study, we identified two rare missense variants in X-linked GRIA3 from male patients who showed syndromes featuring aggressive outbursts. Both G630R and E787G mutations in AMPA receptor GluA3 completely lost their ion channel functions. Furthermore, a guanine-repeat single nucleotide polymorphism (SNP, rs3216834) located in the first intron of human GRIA3 gene was found to regulate GluA3 expression with longer guanine repeats (rs3216834-10G/-11G) suppressing transcription compared to the shorter ones (-7G/-8G/-9G). Importantly, the distribution of rs3216834-10G/-11G was elevated in a male violent criminal sample from Chinese Han population. Using GluA3 knockout mice, we showed that the excitatory neurotransmission and neuronal activity in the medial prefrontal cortex (mPFC) was impaired. Expressing GluA3 back into the mPFC alleviated the aggressive behavior of GluA3 knockout mice, suggesting that the defects in mPFC explained, at least partially, the neural mechanisms underlying the aggressive behavior. Therefore, our study provides compelling evidence that dysfunction of AMPA receptor GluA3 promotes aggressive behavior.

OriginalsprogEngelsk
TidsskriftMolecular Psychiatry
ISSN1359-4184
DOI
StatusE-pub ahead of print - 2022

Bibliografisk note

Funding Information:
We thank Dr. Zhengping Jia in University of Toronto for the generous gift of GluA3 KO mice. Fundings: This work is supported by grants from the National Key R&D Program of China (2019YFA0801603 to Y.S.S. and 2017YFA0105201 to C.Z.), the National Natural Science Foundation of China (32170951 and 91849112 to Y.S.S., 81901161 to J.C., 82171189 and 81971020 to J.J.Y., 31871032 to N.S. and 81901390 to N.L.), the Natural Science Foundation of Jiangsu Province (BE2019707 to Y.S.S.), Special Fund for Science and Technology Innovation Strategy of Guangdong Province (2021B0909050004 to Y.S.S.), the Fundamental Research Funds for the Central Universities (0903-14380029 to Y.S.S.), Strategic Priority Research Program of the Chinese Academy of Sciences (XDPB17 to NS), and Yunnan Applied Basic Research Projects (2019FA008 and 2019FJ003 to N.S.).

Publisher Copyright:
© 2022, The Author(s), under exclusive licence to Springer Nature Limited.

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