Shear stress-dependent expression of apoptosis-regulating genes in endothelial cells

被引:67
作者
Bartling, B
Tostlebe, H
Darmer, D
Holtz, J
Silber, RE
Morawietz, H
机构
[1] Univ Halle Wittenberg, Fac Med, Inst Pathophysiol, D-06097 Halle, Saale, Germany
[2] Univ Halle Wittenberg, Fac Med, Clin Heart & Thorac Surg, D-06097 Halle, Saale, Germany
[3] Univ Halle Wittenberg, Fac Med, Mol Biol Grp, D-06097 Halle, Saale, Germany
关键词
apoptosis; Fas; Bcl-2; family; shear stress; HUVEC;
D O I
10.1006/bbrc.2000.3873
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
Laminar shear stress exerts potent anti-apoptotic effects. Therefore, we analyzed the influence of laminar shear stress on the expression of apoptosis-regulating genes in human umbilical vein endothelial cells (HUVEC). Application of high levels of laminar shear stress (15 and 30 dyn/cm(2)) decreased the susceptibility of HUVEC to undergo apoptosis, whereas low shear stress (1 dyn/cm(2)) had no effect. These diminished signs of apoptosis were accompanied by a decreased mRNA expression of apoptosis-inducing Fas receptor. Furthermore, mRNA and protein expression of anti-apoptotic, soluble Fas isoform FasExo6Del and anti-apoptotic Bcl-x(L) were induced. Surprisingly, high shear stress also elevated mRNA and protein expression of pro-apoptotic Bak. The shear stress-induced up-regulation of Bcl-x(L) and Bak mRNA can be abrogated by inhibition of the endothelial NO synthase. We propose that altered expression of Bcl-x(L) and the Fas system is involved in the protective effect of laminar shear stress against apoptosis in human endothelial cells. (C) 2000 Academic Press.
引用
收藏
页码:740 / 746
页数:7
相关论文
共 31 条
[1]   The role of antiapoptotic Bcl-2 family members in endothelial apoptosis elucidated with antisense oligonucleotides [J].
Ackermann, EJ ;
Taylor, JK ;
Narayana, R ;
Bennett, CF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (16) :11245-11252
[2]  
Bartling B, 1999, CIRCULATION, V100, P216
[3]   Pulsatile stretch and shear stress: Physical stimuli determining the production of endothelium-derived relaxing factors [J].
Busse, R ;
Fleming, I .
JOURNAL OF VASCULAR RESEARCH, 1998, 35 (02) :73-84
[4]   INCREASED ENDOTHELIAL CELL TURNOVER IN AREAS OF IN-VIVO EVANS-BLUE UPTAKE IN PIG AORTA [J].
CAPLAN, BA ;
SCHWARTZ, CJ .
ATHEROSCLEROSIS, 1973, 17 (03) :401-417
[5]  
Cascino I, 1996, J IMMUNOL, V156, P13
[6]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[7]   INDUCTION OF APOPTOSIS BY THE BCL-2 HOMOLOG BAK [J].
CHITTENDEN, T ;
HARRINGTON, EA ;
OCONNOR, R ;
FLEMINGTON, C ;
LUTZ, RJ ;
EVAN, GI ;
GUILD, BC .
NATURE, 1995, 374 (6524) :733-736
[8]   Shear stress inhibits apoptosis of human endothelial cells [J].
Dimmeler, S ;
Haendeler, J ;
Rippmann, V ;
Nehls, M ;
Zeiher, AM .
FEBS LETTERS, 1996, 399 (1-2) :71-74
[9]  
Dimmeler S, 1997, CIRCULATION, V95, P1760
[10]   Suppression of apoptosis by nitric oxide via inhibition of interleukin-1 beta-converting enzyme (ICE)-like and cysteine protease protein (CPP)-32-like proteases [J].
Dimmeler, S ;
Haendeler, J ;
Nehls, M ;
Zeiher, AM .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (04) :601-607