ALUMINUM PERTURBS OSCILLATORY PHOSPHOINOSITIDE-MEDIATED CALCIUM SIGNALING IN HORMONE-STIMULATED HEPATOCYTES

被引:26
作者
SCHOFL, C
SANCHEZBUENO, A
DIXON, CJ
WOODS, NM
LEE, JAC
CUTHBERTSON, KSR
COBBOLD, PH
BIRCHALL, JD
机构
[1] UNIV LIVERPOOL, DEPT HUMAN ANAT & CELL BIOL, POB 147, LIVERPOOL L69 3BX, ENGLAND
[2] ICI PLC, RUNCORN WA7 4QE, CHESHIRE, ENGLAND
基金
英国惠康基金;
关键词
D O I
10.1042/bj2690547
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
Aluminium is known to be toxic to cells from bone, brain and bone marrow but the molecular target(s) affected by Al3+ are not known. We show here that Al3+ disrupts the oscillatory free Ca2+ responses of hepatocytes exposed to the Ca2+-mobilizing agonist phenylephrine. Al3+ initially increases the frequency of the oscillations and later induces broad Ca2+ spikes lasting several minutes. These broad spikes persist after removal of both agonist and Al3+ from the medium. In the absence of agonist, Al3+ has no effect on free Ca2+. The data suggest that some component(s) of the receptor-phosphoinositide-Ca2+ signalling pathway might be the site at which Al3+ exerts toxic effects.
引用
收藏
页码:547 / 550
页数:4
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