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M1 muscarinic receptor facilitates cognitive function by interplay with AMPA receptor GluAl subunit

M1 muscarinic acetylcholine receptors (M1 mAChRs) are the most abundant muscarinic receptors in the hippocampus and have been shown to have procognitive effects. AMPA receptors (AMPARs), an important subtype of ionotropic glutamate receptors, are key components in neurocognitive networks. However, t...

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Bibliographic Details
Published in:The FASEB journal 2018-08, Vol.32 (8), p.4247-4257
Main Authors: Zhao, Lan‐Xue, Ge, Yan‐Hui, Xiong, Cai‐Hong, Tang, Ling, Yan, Ying‐Hui, Law, Ping‐Yee, Qiu, Yu, Chen, Hong‐Zhuan
Format: Article
Language:English
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Summary:M1 muscarinic acetylcholine receptors (M1 mAChRs) are the most abundant muscarinic receptors in the hippocampus and have been shown to have procognitive effects. AMPA receptors (AMPARs), an important subtype of ionotropic glutamate receptors, are key components in neurocognitive networks. However, the role of AMPARs in procognitive effects of M1 mAChRs and how M1 mAChRs affect the function of AMPARs remain poorly understood. Here, we found that basal expression of GluA1, a subunit of AMPARs, and its phosphorylation at Ser845 were maintained by M1 mAChR activity. Activation of M1 mAChRs promoted membrane insertion of GluA1, especially to postsynaptic densities. Impairment of hippocampus‐dependent learning and memory by antagonism of M1 mAChRs paralleled the reduction of GluA1 expression, and improvement of learning and memory by activation of M1 mAChRs was accompanied by the synaptic insertion of GluA1 and its increased phosphorylation at Ser845. Furthermore, abrogation of phosphorylation of Ser845 residue of GluA1 ablated M1 mAChR‐mediated improvement of learning and memory. Taken together, these results show a functional correlation of M1 mAChRs and GluA1 and the essential role of GluA1 in M1 mAChR‐mediated cognitive improvement.—Zhao, L.‐X., Ge, Y.‐H., Xiong, C.‐H., Tang, L., Yan, Y.‐H., Law, P.‐Y., Qiu, Y., Chen, H.‐Z. M1 muscarinic receptor facilitates cognitive function by interplay with AMPA receptor GluA1 subunit. FASEB J. 32, 4247‐4257 (2018). www.fasebj.org
ISSN:0892-6638
1530-6860
DOI:10.1096/fj.201800029R