Oxytocin-induced phosphorylation of myosin light chain is mediated by extracellular calcium influx in pregnant rat myometrium

被引:13
|
作者
Shojo, H
Kaneko, Y
机构
[1] Boston Univ, Sch Med, Whitaker Cardiovasc Inst, Mol Genet Sect, Boston, MA 02118 USA
[2] Saga Med Sch, Dept Forens Sci, Saga 8498501, Japan
关键词
intracellular free Ca2+; L-type voltage-dependent Ca2+ channel; myometrial contraction; myosin light chain; oxytocin; oxytocin receptor;
D O I
10.1002/jmr.551
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
Studies of oxytocin-induced phosphorylation of myosin light chain (MLC), resulting in myometrial contraction, suggest that extracellular Ca2+ influx is involved in its signal transduction. To explore the possibility that intracellular Ca2+ mobilization by oxytocin may also contribute to MLC phosphorylation, we investigated the relative contributions of these Ca2+ sources to oxytocin signal transduction in myometrium of pregnant rat. In pregnant rat myometrium, oxytocin-induced Ca2+ influx occurs via an L-type voltage-dependent Ca2+ channel. Treatment with verapamil, an antagonist specific for these channels, significantly diminished MLC phosphorylation observed in response to oxytocin administration without affecting the release of Ca2+ from intracellular Ca2+ stores. Furthermore, oxytocin-induced MLC phosphorylation was not observed when extracellular Ca2+ was not present. Our results clearly indicate that extracellular Ca2+ influx, rather than release from Ca2+ storage sites, is essential for oxytocin-induced MLC phosphorylation. Copyright (C) 2001 John Wiley Sons, Ltd.
引用
收藏
页码:401 / 405
页数:5
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