Ceramide triggers intracellular calcium release via the IP3 receptor in Xenopus laevis oocytes

被引:29
作者
Kobrinsky, E
Spielman, AI
Rosenzweig, S
Marks, AR
机构
[1] Columbia Univ Coll Phys & Surg, Mol Cardiol Program, Div Cardiol, Dept Med, New York, NY 10032 USA
[2] Columbia Univ Coll Phys & Surg, Dept Med, Div Circulatory Physiol, New York, NY 10032 USA
[3] Columbia Univ Coll Phys & Surg, Dept Pharmacol, New York, NY 10032 USA
[4] NYU, Coll Dent, Div Basic Sci, New York, NY 10010 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 1999年 / 277卷 / 04期
关键词
meiotic maturation; calcium signaling; phospholipase C;
D O I
10.1152/ajpcell.1999.277.4.C665
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Ceramide, a product of sphingomyelin turnover, is a lipid second messenger that mediates diverse signaling pathways, including those leading to cell cycle arrest and differentiation. The mechanism(s) by which ceramide signals downstream events have not been fully elucidated. Here we show that, in Xenopus laevis oocytes, ceramide-induced maturation is associated with the release of intracellular calcium stores. Ceramide caused a dose-dependent elevation in the second messenger inositol 1,4,5-trisphosphate (IP3) via activation of G(q/11)alpha and phospholipase C-beta X Elevation of IP3, in turn, activated the IP3 receptor calcium release channel on the endoplasmic reticulum, resulting in a rise in cytoplasmic calcium. Thus our study demonstrates that cross talk between the ceramide and phosphoinositide signaling pathways modulates intracellular calcium homeostasis.
引用
收藏
页码:C665 / C672
页数:8
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