Wei, Shoupeng;
Jiang, Jian;
Wang, Dilong;
Chang, Jinlong;
Tian, Liusuyan;
Yang, Xiuyan;
Ma, Xiao-Ru;
... Li, Ningning; + view all
(2024)
GPR158 in pyramidal neurons mediates social novelty behavior via modulating synaptic transmission in male mice.
Cell Reports
, 43
(10)
, Article 114796. 10.1016/j.celrep.2024.114796.
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Abstract
Impairment in social communication skills is a hallmark feature of autism spectrum disorder (ASD). The role of G-protein-coupled receptor 158 (GPR158) in ASD remains largely unexplored. In this study, we observed that both constitutive and cell-/tissue-specific knockouts of Gpr158 in pyramidal neurons or the medial prefrontal cortex (mPFC) result in impaired novelty preference, while sociability remains unaffected in male mice. Notably, the loss of GPR158 leads to a significant decline in excitatory synaptic transmission, characterized by a reduction in glutamate vesicles, as well as the expression and phosphorylation of GluN2B in the mPFC. We successfully rescue the phenotype of social novelty deficits either by reintroducing GPR158 in the mPFC of Gpr158 deficient mice or by chemogenetic activation of pyramidal neurons where Gpr158 is specifically ablated. Our findings indicate that GPR158 in pyramidal neurons plays a specific role in modulating social novelty and may represent a potential target for treating social disorders.
Type: | Article |
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Title: | GPR158 in pyramidal neurons mediates social novelty behavior via modulating synaptic transmission in male mice |
Open access status: | An open access version is available from UCL Discovery |
DOI: | 10.1016/j.celrep.2024.114796 |
Publisher version: | https://doi.org/10.1016/j.celrep.2024.114796 |
Language: | English |
Additional information: | © 2024 The Author(s). Published by Elsevier Inc. This is an open access article under the CC BY-NC license (http://creativecommons.org/licenses/by-nc/4.0/). |
Keywords: | GPR158, social novelty, pyramidal neurons, synaptic transmission, medial prefrontal cortex |
UCL classification: | UCL UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences > Div of Medicine UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences > Div of Medicine > Wolfson Inst for Biomedical Research |
URI: | https://discovery.ucl.ac.uk/id/eprint/10198309 |




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