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Expression of TRPC3 in Chinese Hamster Ovary Cells Results in Calcium-activated Cation Currents Not Related to Store Depletion

TRPC3 (or Htrp3) is a human member of the trp family of Ca(2+)-permeable cation channels. Since expression of TRPC3 cDNA results in markedly enhanced Ca(2+) influx in response to stimulation of membrane receptors linked to phospholipase C (Zhu, X., J. Meisheng, M. Peyton, G. Bouley, R. Hurst, E. Ste...

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Detalles Bibliográficos
Autores principales: Zitt, Christof, Obukhov, Alexander G., Strübing, Carsten, Zobel, Andrea, Kalkbrenner, Frank, Lückhoff, Andreas, Schultz, Günter
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1997
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2132548/
https://www.ncbi.nlm.nih.gov/pubmed/9298988
Descripción
Sumario:TRPC3 (or Htrp3) is a human member of the trp family of Ca(2+)-permeable cation channels. Since expression of TRPC3 cDNA results in markedly enhanced Ca(2+) influx in response to stimulation of membrane receptors linked to phospholipase C (Zhu, X., J. Meisheng, M. Peyton, G. Bouley, R. Hurst, E. Stefani, and L. Birnbaumer. 1996. Cell. 85:661–671), we tested whether TRPC3 might represent a Ca(2+) entry pathway activated as a consequence of depletion of intracellular calcium stores. CHO cells expressing TRPC3 after intranuclear injection of cDNA coding for TRPC3 were identified by fluorescence from green fluorescent protein. Expression of TRPC3 produced cation currents with little selectivity for Ca(2+) over Na(+). These currents were constitutively active, not enhanced by depletion of calcium stores with inositol-1,4,5-trisphosphate or thapsigargin, and attenuated by strong intracellular Ca(2+) buffering. Ionomycin led to profound increases of currents, but this effect was strictly dependent on the presence of extracellular Ca(2+). Likewise, infusion of Ca(2+) into cell through the patch pipette increased TRPC3 currents. Therefore, TRPC3 is stimulated by a Ca(2+)-dependent mechanism. Studies on TRPC3 in inside-out patches showed cation-selective channels with 60-pS conductance and short (<2 ms) mean open times. Application of ionomycin to cells increased channel activity in cell-attached patches. Increasing the Ca(2+) concentration on the cytosolic side of inside-out patches (from 0 to 1 and 30 μM), however, failed to stimulate channel activity, even in the presence of calmodulin (0.2 μM). We conclude that TRPC3 codes for a Ca(2+)-permeable channel that supports Ca(2+)-induced Ca(2+)-entry but should not be considered store operated.