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Functional characteristics of TRPC4 channels expressed in HEK 293 cells

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dc.contributor.authorSung, Tae Sik-
dc.contributor.authorKim, Min Ji-
dc.contributor.authorJeon, Jae-Pyo-
dc.contributor.authorKim, Byung Joo-
dc.contributor.authorHong, Soojin-
dc.contributor.authorJeon, Ju-Hong-
dc.contributor.authorSo, Insuk-
dc.contributor.authorKim, Seon Jeong-
dc.date.accessioned2012-05-22T07:06:19Z-
dc.date.available2012-05-22T07:06:19Z-
dc.date.issued2009-02-
dc.identifier.citationMOLECULES AND CELLS; Vol.27 2; 167-173ko_KR
dc.identifier.issn1016-8478-
dc.identifier.urihttps://hdl.handle.net/10371/76246-
dc.description.abstractThe 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 GTP gamma S was not desensitized. TPRC4 activation by GTP gamma S 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 GTP gamma S was inhibited by the calmodulin inhibitor W-7. We conclude that TRPC4 and TRPC5 have different properties and their own physiological roles.ko_KR
dc.language.isoenko_KR
dc.publisherKOREAN SOC MOLECULAR & CELLULAR BIOLOGYko_KR
dc.subjectdesensitizationko_KR
dc.subjectpHko_KR
dc.subjectnonselective cation channelko_KR
dc.subjecttransient receptor potential channelko_KR
dc.subjectTRPC5ko_KR
dc.subjectTRPC4ko_KR
dc.titleFunctional characteristics of TRPC4 channels expressed in HEK 293 cellsko_KR
dc.typeArticleko_KR
dc.contributor.AlternativeAuthor성태식-
dc.contributor.AlternativeAuthor전재표-
dc.contributor.AlternativeAuthor전주홍-
dc.contributor.AlternativeAuthor소인석-
dc.contributor.AlternativeAuthor김선정-
dc.contributor.AlternativeAuthor김병주-
dc.contributor.AlternativeAuthor홍수진-
dc.contributor.AlternativeAuthor김민지-
dc.identifier.doi10.1007/s10059-009-0021-3-
dc.citation.journaltitleMOLECULES AND CELLS-
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