Regulation of [Ca2+]i homeostasis in MRP1 overexpressing cells

被引:10
作者
Filipeanu, CM
Nelemans, A
Veldman, RJ
de Zeeuw, D
Kok, JW
机构
[1] Univ Groningen, Dept Physiol Chem, NL-9713 AV Groningen, Netherlands
[2] Univ Groningen, Inst Drug Explorat, GUIDE, Dept Clin Pharmacol, NL-9713 AV Groningen, Netherlands
关键词
multidrug resistance protein; capacitative Ca2+ entry; HT29; cell; GLC4; MK571; D; L-Threo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol;
D O I
10.1016/S0014-5793(00)01585-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Regulation of capacitative Ca2+ entry,vas studied in two different multidrug resistance (MDR) protein (MRP1) overexpressing cell lines, HT29(col) and GLC4/ADR. MRP1 overexpression was accompanied by a decreased response to thapsigargin, Moreover, inhibition of capacitative Ca2+ entry by D,L-threo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol (PDMP) was abolished in MRP1 overexpressing cells. Both PDMP and the MRP1 inhibitor MK571 greatly reduced InsP(3)-mediated Ca-45(2+) release from intracellular stores in HT29 cells. Again, these effects were virtually abolished in HT29(col) cells. Our results point to a modulatory role of MRP1 on intracellular calcium concentration ([Ca2+](i)) homeostasis which may contribute to the MDR phenotype, (C) 2000 Federation of European Biochemical Societies.
引用
收藏
页码:107 / 110
页数:4
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