TY - JOUR
T1 - TRPC1 is required for functional store-operated Ca2+ channels
T2 - Role of acidic amino acid residues in the S5-S6 region
AU - Liu, Xibao
AU - Singh, Brij B.
AU - Ambudkar, Indu S.
PY - 2003/3/28
Y1 - 2003/3/28
N2 - The exact role of TRPC1 in store-operated calcium influx channel (SOCC) function is not known. We have examined the effect of overexpression of full-length TRPC1, depletion of endogenous TRPC1, and expression of TRPC1 in which the proposed pore region (S5-S6, amino acids (aa) 557-620) was deleted or modified by site-directed mutagenesis on thapsigargin- and carbachol-stimulated SOCC activity in HSG cells. TRPC1 overexpression induced channel activity that was indistinguishable from the endogenous SOCC activity. Transfection with antisense hTRPC1 decreased SOCC activity although characteristics of SOCC-mediated current, ISOC, were not altered. Expression of TRPC1Δ567-793, but not TRPC1Δ664-793, induced a similar decrease in SOCC activity. Furthermore, TRPC1Δ567-793 was co-immunoprecipitated with endogenous TRPC1. Simultaneous substitutions of seven acidic aa in the S5-S6 region (Asp → Asn and Glu → Gln) decreased SOCC-mediated Ca2+, but not Na+, current and induced a left shift in Erev. Similar effects were induced by E576K or D581K, but not D581N or E615K, substitution. Furthermore, expressed TRPC1 proteins interacted with each other. Together, these data demonstrate that TRPC1 is required for generation of functional SOCC in HSG cells. We suggest that TRPC1 monomers co-assemble to form SOCC and that specific acidic aa residues in the proposed pore region of TRPC1 contribute to Ca2+ influx.
AB - The exact role of TRPC1 in store-operated calcium influx channel (SOCC) function is not known. We have examined the effect of overexpression of full-length TRPC1, depletion of endogenous TRPC1, and expression of TRPC1 in which the proposed pore region (S5-S6, amino acids (aa) 557-620) was deleted or modified by site-directed mutagenesis on thapsigargin- and carbachol-stimulated SOCC activity in HSG cells. TRPC1 overexpression induced channel activity that was indistinguishable from the endogenous SOCC activity. Transfection with antisense hTRPC1 decreased SOCC activity although characteristics of SOCC-mediated current, ISOC, were not altered. Expression of TRPC1Δ567-793, but not TRPC1Δ664-793, induced a similar decrease in SOCC activity. Furthermore, TRPC1Δ567-793 was co-immunoprecipitated with endogenous TRPC1. Simultaneous substitutions of seven acidic aa in the S5-S6 region (Asp → Asn and Glu → Gln) decreased SOCC-mediated Ca2+, but not Na+, current and induced a left shift in Erev. Similar effects were induced by E576K or D581K, but not D581N or E615K, substitution. Furthermore, expressed TRPC1 proteins interacted with each other. Together, these data demonstrate that TRPC1 is required for generation of functional SOCC in HSG cells. We suggest that TRPC1 monomers co-assemble to form SOCC and that specific acidic aa residues in the proposed pore region of TRPC1 contribute to Ca2+ influx.
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U2 - 10.1074/jbc.M213271200
DO - 10.1074/jbc.M213271200
M3 - Article
C2 - 12536150
AN - SCOPUS:0037648508
SN - 0021-9258
VL - 278
SP - 11337
EP - 11343
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 13
ER -