Shear stress activates cytosolic phospholipase A(2) (cPLA(2)) and MAP kinase in human endothelial cells

被引:106
作者
Pearce, MJ
McIntyre, TM
Prescott, SM
Zimmerman, GA
Whatley, RE
机构
[1] UNIV UTAH, SCH MED, PROGRAM HUMAN MOLEC BIOL & GENET, SALT LAKE CITY, UT 84112 USA
[2] UNIV UTAH, SCH MED, DEPT BIOCHEM, SALT LAKE CITY, UT 84112 USA
[3] UNIV UTAH, SCH MED, DEPT MED, SALT LAKE CITY, UT 84112 USA
[4] UNIV UTAH, SCH MED, DEPT PATHOL, SALT LAKE CITY, UT 84112 USA
[5] E CAROLINA UNIV, SCH MED, DEPT MED, GREENVILLE, NC 27858 USA
关键词
D O I
10.1006/bbrc.1996.0089
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 signalling events that govern endothelial responses to shear are incompletely defined. In this study confluent human endothelial cells were subjected to shear. At shear levels of 1.04, 2.92, 5.31 and 8.3 dynes/cm(2), which are in the range of those that occur in vessels in venous and arterial circulations, the activity of cPLA(2) was increased above control levels. To examine pathways by which cPLA, may be activated in response to shear, we assayed the p42 isoform of MAP kinase (ERK-2) and found increased activity in cells exposed to shear. Our findings demonstrate for the first time that cPLA(2) and MAP kinase p42 are activated by shear in human endothelial cells, and add to evidence from other systems that indicates that the two enzymes have related signalling functions. (C) 1996 Academic Press, Inc.
引用
收藏
页码:500 / 504
页数:5
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