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The specific activation of TRPC4 by Gi protein subtype

Cited 31 time in Web of Science Cited 33 time in Scopus
Authors

Jeon, Jae-Pyo; Lee, Kyu Pil; Park, Eun Jung; Sung, Tae Sik; Kim, Byung Joo; Jeon, Ju-Hong; So, Insuk

Issue Date
2008-10-16
Publisher
Elsevier
Citation
Biochem Biophys Res Commun. 377 (2008) 538-543
Keywords
AnimalsCalcium Channels/genetics/metabolismCell LineGTP-Binding Protein alpha Subunit, Gi2/antagonists & inhibitors/genetics/*metabolismGuanosine 5'-O-(3-Thiotriphosphate)/metabolism/pharmacologyHumansMiceReceptor, Muscarinic M2/geneticsTRPC Cation Channels/*agonists/metabolismTRPV Cation Channels/genetics/metabolism
Abstract
The classical type of transient receptor potential channel (TRPC) is a molecular candidate for Ca(2+)-permeable cation channels in mammalian cells. Especially, TRPC4 has the similar properties to Ca(2+)-permeable nonselective cation channels (NSCCs) activated by muscarinic stimulation in visceral smooth muscles. In visceral smooth muscles, NSCCs activated by muscarinic stimulation were blocked by anti-Galphai/o antibodies. However, there is still no report which Galpha proteins are involved in the activation process of TRPC4. Among Galpha proteins, only Galphai protein can activate TRPC4 channel. The activation effect of Galphai was specific for TRPC4 because Galphai has no activation effect on TRPC5, TRPC6 and TRPV6. Coexpression with muscarinic receptor M2 induced TRPC4 current activation by muscarinic stimulation with carbachol, which was inhibited by pertussis toxin. These results suggest that Galphai is involved specifically in the activation of TRPC4.
ISSN
1090-2104 (Electronic)
Language
English
URI
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=18854172

http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6WBK-4TNGBN3-6-9&_cdi=6713&_user=168665&_orig=search&_coverDate=12%2F12%2F2008&_sk=996229997&view=c&wchp=dGLbVlb-zSkzV&md5=6b934df55670501c229a9c7fdff07b93&ie=/sdarticle.pdf

https://hdl.handle.net/10371/68127
DOI
https://doi.org/10.1016/j.bbrc.2008.10.012
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