COUPLING OF MUSCARINIC RECEPTORS TO THE MOBILIZATION OF INTRACELLULAR CA-2+ STORES IN PERMEABILIZED SH-SY5Y HUMAN NEUROBLASTOMA-CELLS

被引:28
|
作者
WOJCIKIEWICZ, RJH
SAFRANY, ST
CHALLISS, RAJ
STRUPISH, J
NAHORSKI, SR
机构
[1] Department of Pharmacology, University of Leicester, Leicester LE1 9HN, University Road
基金
英国惠康基金;
关键词
D O I
10.1042/bj2720269
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
Intracellular stores of Ca2+ were mobilized transiently by carbachol in suspensions of electrically permeabilized SH-SY5Y cells. The kinetics and the dose-dependence of this mobilization paralleled carbachol-induced increases in inositol 1,4,5-trisphosphate (InsP3) mass [for both parameters EC50 (concn. giving half-maximal response) = 60-70 μM]. Guanosine 5'-[γ-thio]triphosphate enhanced the maximal effect and the potency of carbachol on Ca2+ mobilization and InsP3 mass, but caused separation of the dose-response curves (EC50 = 0.6 μM and 5.6 μM respectively). These data show that functional coupling of muscarinic receptors to Ca2+ mobilization can be maintained after permeabilization, reveal major effects of guanine nucleotides on agonist-induced Ca2+ mobilization and provide a basis for explanation of discrepancies between agonist potency on InsP3 concentration and Ca2+ mobilization in intact cells.
引用
收藏
页码:269 / 272
页数:4
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