Your browser doesn't support javascript.
loading
Shear stress-dependent expression of apoptosis-regulating genes in endothelial cells.
Bartling, B; Tostlebe, H; Darmer, D; Holtz, J; Silber, R E; Morawietz, H.
Affiliation
  • Bartling B; Clinic for Heart and Thoracic Surgery, Institute of Pathophysiology, Halle (Saale), D-06097, Germany.
Biochem Biophys Res Commun ; 278(3): 740-6, 2000 Nov 30.
Article de En | MEDLINE | ID: mdl-11095978
ABSTRACT
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.
Sujet(s)
Recherche sur Google
Collection: 01-internacional Base de données: MEDLINE Sujet principal: Endothélium vasculaire / Régulation de l'expression des gènes / Apoptose Limites: Humans Langue: En Journal: Biochem Biophys Res Commun Année: 2000 Type de document: Article Pays d'affiliation: Allemagne
Recherche sur Google
Collection: 01-internacional Base de données: MEDLINE Sujet principal: Endothélium vasculaire / Régulation de l'expression des gènes / Apoptose Limites: Humans Langue: En Journal: Biochem Biophys Res Commun Année: 2000 Type de document: Article Pays d'affiliation: Allemagne