Direct coupling between arachidonic acid-induced Ca2+ release and Ca2+ entry in HEK293 cells

被引:8
|
作者
Luo, DL [1 ]
Sun, HL
Lan, XM
Xiao, RP
Han, Q
机构
[1] Peking Univ, Hlth Sci Ctr, Inst Cardiovasc Sci, Beijing 100083, Peoples R China
[2] NIA, Gerontol Res Ctr, NIH, Baltimore, MD 21224 USA
关键词
arachidonic acid; Ca2+ release; Ca2+ entry; Gd3+; coupling; isotetrandrine;
D O I
10.1016/j.prostaglandins.2004.11.004
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
Arachidonic acid (AA) modulates intracellular Ca2+ signaling via Ca2+ release or/and Ca2+ entry. However, the mechanism underlies either process is unknown; nor is it clear as to whether the two processes are mechanistically linked. By using Fura2/AM, we found that AA induced mobilization of internal Ca2+ store and an increment in Ca2+, Mn2+ and Ba2+ influx in HEK293 cells. The AA-mediated Ca2+ signaling was not due to AA metabolites, and insensitive to capacitative Ca2+ entry inhibitors. Interestingly, isotetrandrine and Gd3+ inhibited both AA-induced Ca2+ release and Ca2+ entry in a concentration-dependent manner without affecting Ca2+ discharge caused by carbachol, caffeine, or thapsigargin. Additionally, similar pattern of inhibition was observed with tetracaine treatment. More importantly, the three compounds exhibited almost equal potent inhibition of AA-initiated Ca2+ release as well as Ca2+ influx. Therefore, this study, for the first time, provides evidence for a direct coupling between AA-mediated Ca2+ release and Ca2+ entry. (c) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:141 / 151
页数:11
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