Authors
Jae-Pyo Jeon, Seung-Eon Roh, Jinhong Wie, Jinsung Kim, Hana Kim, Kyu-Pil Lee, Dongki Yang, Ju-Hong Jeon, Nam-Hyuk Cho, In-Gyu Kim, David E Kang, Hyun Jin Kim, Insuk So
Publication date
2013/10/1
Journal
Cell Calcium
Volume
54
Issue
4
Pages
307-319
Publisher
Churchill Livingstone
Description
The ubiquitous transient receptor potential canonical (TRPC) channels function as non-selective, Ca2+-permeable channels. TRPC channels are activated by stimulation of Gαq-PLC-coupled receptors. Here, we report that TRPC4/TRPC5 can be activated by Gαi. We studied the essential role of Gαi subunits in TRPC4 activation and investigated changes in ion selectivity and pore dilation of the TRPC4 channel elicited by the Gαi2 subunit. Activation of TRPC4 by Gαi2 increased Ca2+ permeability and Ca2+ influx through TRPC4 channels. Co-expression of the muscarinic receptor (M2) and TRPC4 in HEK293 cells induced TRPC4-mediated Ca2+ influx. Moreover, both TRPC4β and the TRPC4β-Gαi2 signaling complex induced inhibition of neurite growth and arborization in cultured hippocampal neurons. Cells treated with KN-93, a CaMKII inhibitor, prevented TRPC4- and TRPC4-Gαi2Q205L-mediated inhibition of …
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