TRPC3 mediates T-cell receptor-dependent calcium entry in human T-lymphocytes |
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Authors: | Philipp Stephan Strauss Bettina Hirnet Daniela Wissenbach Ulrich Mery Laurence Flockerzi Veit Hoth Markus |
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Affiliation: | Institut für experimentelle und klinische Pharmakologie und Toxikologie and the Institut für Physiologie, Geb?ude 58, Universit?t des Saarlandes, D-66421 Homburg/Saar, Germany. stephan.philipp@uniklinik-saarland.de |
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Abstract: | ![]() Stimulation of the T-cell receptor (TCR) activates Ca2+ entry across the plasma membrane, which is a key triggering event for the T-cell-associated immune response. We show that TRPC3 channels are important for the TCR-dependent Ca2+ entry pathway. The TRPC3 gene was found to be damaged in human T-cell mutants defective in Ca2+ influx. Mutations of the TRPC3 gene were accompanied by changes of TRPC3 gene expression. Introduction of the complete human TRPC3 cDNA into those mutants rescued Ca2+ currents as well as TCR-dependent Ca2+ signals. Our data provide the initial step toward understanding the molecular nature of endogenous Ca2+ channels participating in T-cell activation and put forward TRPC3 as a new target for modulating the immune response. |
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