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Functional characteristics of TRPC4 channels expressed in HEK 293 cells

Cited 7 time in Web of Science Cited 8 time in Scopus
Authors

Sung, Tae Sik; Kim, Min Ji; Hong, Soojin; Jeon, Jae-Pyo; Kim, Byung Joo; Jeon, Ju-Hong; Kim, Seon Jeong; So, Insuk

Issue Date
2009-03-12
Publisher
Springer Verlag
Citation
Mol Cells. 27(2), 167-173
Keywords
Calcium-Calmodulin-Dependent Protein Kinases/antagonists & inhibitorsCells, CulturedEnzyme Inhibitors/pharmacologyGuanosine 5'-O-(3-Thiotriphosphate)/pharmacologyHumansKidney/cytology/*metabolismReceptors, Muscarinic/genetics/metabolismSulfonamides/pharmacologyTRPC Cation Channels/genetics/*metabolism
Abstract
The classical type of transient receptor potential (TRPC) channel is a molecular candidate for Ca(2+)-permeable cation channels in mammalian cells. Because TRPC4 and TRPC5 belong to the same subfamily of TRPC, they have been assumed to have the same physiological properties. However, we found that TRPC4 had its own functional characteristics different from those of TRPC5. TRPC4 channels had no constitutive activity and were activated by muscarinic stimulation only when a muscarinic receptor was co-expressed with TRPC4 in human embryonic kidney (HEK) cells. Endogenous muscarinic receptor appeared not to interact with TRPC4. TPRC4 activation by GTPgammaS was not desensitized. TPRC4 activation by GTPgammaS was not inhibited by either Rho kinase inhibitor or MLCK inhibitor. TRPC4 was sensitive to external pH with pK (a) of 7.3. Finally, TPRC4 activation by GTPgammaS was inhibited by the calmodulin inhibitor W-7. We conclude that TRPC4 and TRPC5 have different properties and their own physiological roles.
ISSN
1016-8478 (Print)
Language
English
URI
http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=19277498

http://www.springerlink.com/content/dq72777021630516/fulltext.pdf

https://hdl.handle.net/10371/68368
DOI
https://doi.org/10.1007/s10059-009-0021-3
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