{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,6]],"date-time":"2026-10-06T09:11:42Z","timestamp":1791277902010,"version":"4.1.0"},"reference-count":43,"publisher":"Portland Press Ltd.","issue":"2","content-domain":{"domain":["portlandpress.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2009,6,1]]},"abstract":"<jats:p>TRPC (canonical transient receptor potential) channel subunits have been shown to assemble into homo- or hetero-meric channel complexes, including different Ca2+-handling proteins, required for the activation of CCE (capacitative Ca2+ entry) or NCCE (non-CCE) pathways. In the present study we found evidence for the dynamic interaction between endogenously expressed hTRPC6 (human TRPC6) with either both Orai1 and STIM1 (stromal interaction molecule 1) or hTRPC3 to participate in CCE or NCCE. Electrotransjection of cells with an anti-hTRPC6 antibody, directed towards the C-terminal region, reduces CCE induced by TPEN [N,N,N\u2032,N\u2032-tetrakis-(2-pyridylmethyl)-ethylenediamine], which reduces the intraluminal free Ca2+ concentration. Cell stimulation with thrombin or extensive Ca2+-store depletion by TG (thapsigargin)+ionomycin enhanced the interaction between hTRPC6 and the CCE proteins Orai1 and STIM1. In contrast, stimulation with the diacylglycerol analogue OAG (1-oleoyl-2-acetyl-sn-glycerol) displaces hTRPC6 from Orai1 and STIM1 and enhances the association between hTRPC6 and hTRPC3. The interaction between hTRPC6 and hTRPC3 was abolished by dimethyl-BAPTA [1,2-bis-(o-aminophenoxy)ethane-N,N,N\u2032,N\u2032-tetra-acetic acid] loading, which indicates that this phenomenon is Ca2+-dependent. These findings support the hypothesis that hTRPC6 participates both in CCE and NCCE through its interaction with the Orai1\u2013STIM1 complex or hTRPC3 respectively.<\/jats:p>","DOI":"10.1042\/bj20082179","type":"journal-article","created":{"date-parts":[[2009,3,5]],"date-time":"2009-03-05T15:00:20Z","timestamp":1236265220000},"page":"267-277","update-policy":"https:\/\/doi.org\/10.1042\/crossmark_policy","source":"Crossref","is-referenced-by-count":91,"title":["Dynamic interaction of hTRPC6 with the Orai1\u2013STIM1 complex or hTRPC3 mediates its role in capacitative or non-capacitative Ca2+ entry pathways"],"prefix":"10.1042","volume":"420","author":[{"given":"Isaac","family":"Jardin","sequence":"first","affiliation":[{"name":"Department of Physiology (Cellular Physiology Research Group), University of Extremadura, 10071 Caceres, Spain"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Luis\u00a0J.","family":"G\u00f3mez","sequence":"additional","affiliation":[{"name":"Department of Physiology (Cellular Physiology Research Group), University of Extremadura, 10071 Caceres, Spain"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Gines\u00a0M.","family":"Salido","sequence":"additional","affiliation":[{"name":"Department of Physiology (Cellular Physiology Research Group), University of Extremadura, 10071 Caceres, Spain"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Juan\u00a0A.","family":"Rosado","sequence":"additional","affiliation":[{"name":"Department of Physiology (Cellular Physiology Research Group), University of Extremadura, 10071 Caceres, Spain"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"288","published-online":{"date-parts":[[2009,5,13]]},"reference":[{"key":"2021112214212531000_B1","doi-asserted-by":"crossref","first-page":"409","DOI":"10.1016\/S0143-4160(03)00053-8","article-title":"The venerable inveterate invertebrate TRP channels","volume":"33","author":"Montell","year":"2003","journal-title":"Cell Calcium"},{"key":"2021112214212531000_B2","doi-asserted-by":"crossref","first-page":"12935","DOI":"10.1074\/jbc.C800008200","article-title":"Functional requirement for Orai1 in store-operated TRPC1\u2013STIM1 channels","volume":"283","author":"Cheng","year":"2008","journal-title":"J. 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