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Regulation of Src family kinases by muscarinic acetylcholine receptors in heterologous cells and neurons.

Authors :
Li-Min Mao
Lexi Young
Xiang-Ping Chu
Wang, John Q.
Source :
Frontiers in Molecular Neuroscience; 2024, p1-8, 8p
Publication Year :
2024

Abstract

Five muscarinic acetylcholine (mACh) receptor subtypes are divided into two classes: the M1 class (M<subscript>1</subscript>, M<subscript>3</subscript>, and M<subscript>5</subscript>) and the M2 class (M<subscript>2</subscript> and M<subscript>4</subscript>). The former is coupled to G<subscript>q</subscript> proteins, while the latter is coupled to G<subscript>i/o</subscript> proteins. Accumulating evidence indicates that mACh receptors play a significant role in the regulation of the Src family kinase (SFK), a subfamily of non-receptor tyrosine kinases. mACh receptors exert their roles in a subtype-dependent fashion and preferentially target Src and Fyn, two members of SFKs that are expressed in the brain and enriched at synaptic sites. While the M<subscript>1</subscript> receptor positively modulates SFK activity, the M<subscript>4</subscript> receptor inhibits it. By modulating SFKs, mACh receptors are actively involved in the regulation of expression and function of a variety of receptors, structural proteins, and signaling molecules. In particular, the M<subscript>4</subscript> receptor and the dopamine D<subscript>1</subscript> receptor are coexpressed in striatonigral projection neurons of the striatum. G<subscript>i/o</subscript>-coupled M<subscript>4</subscript> and G<subscript>q</subscript>-coupled D<subscript>1</subscript> receptors antagonistically regulate SFK activity, thereby forming a dynamic balance controlling glutamate receptor activity, excitability of neurons, and synaptic plasticity. In summary, mACh receptors play a crucial role in regulating SFK activity in heterologous cells and neurons. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16625099
Database :
Complementary Index
Journal :
Frontiers in Molecular Neuroscience
Publication Type :
Academic Journal
Accession number :
175121098
Full Text :
https://doi.org/10.3389/fnmol.2023.1340725