Flow-mediated signaling modulates endothelial cell phenotype

被引:34
作者
Garin, Gwenaele
Berk, Bradford C.
机构
[1] Univ Rochester, Inst Cardiovasc Res, Rochester, NY 14642 USA
[2] Univ Rochester, Dept Med, Rochester, NY USA
来源
ENDOTHELIUM-JOURNAL OF ENDOTHELIAL CELL RESEARCH | 2006年 / 13卷 / 06期
关键词
endothelial cells; ERK5; KLF-2; PECAM-1; shear tress;
D O I
10.1080/10623320601061599
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The focal development of atherosclerosis in the vascular tree may be explained in part by the local nature of blood flow. Bifurcations and branching points, prone to early atherogenesis, experience disturbed and oscillatory flow, whereas straight vascular regions, resistant to atherosclerosis, are exposed to steady laminar flow. A large number of studies suggest that the antiatherosclerotic effects of laminar flow are in part due to the ability of flow to modulate endothelial cell phenotype. Under steady laminar flow, endothelial cells generate molecules that promote a vasoactive, anticoagulant, anti-inflammatory, and growth - inhibitory surface. In contrast, disturbed How induces a proliferative, prothrombotic, and adhesive phenotype. Endothelial cells are able to sense the variations of flow via mechanosensitive cell surface proteins and to transduce these signals via intracellular pathways to transcription factors in the nucleus leading to phenotypic changes. This review summarizes the "outside-in" signaling events initiated by flow that modulate endothelial cell phenotype.
引用
收藏
页码:375 / 384
页数:10
相关论文
共 106 条
[21]   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
[22]   Gab1, SHP2, and protein kinase a are crucial for the activation of the endothelial NO synthase by fluid shear stress [J].
Dixit, M ;
Loot, AE ;
Mohamed, A ;
Fisslthaler, B ;
Boulanger, CM ;
Ceacareanu, B ;
Hassid, A ;
Busse, R ;
Fleming, I .
CIRCULATION RESEARCH, 2005, 97 (12) :1236-1244
[23]   In vivo induction of endothelial apoptosis leads to vessel thrombosis and endothelial denudation - A clue to the understanding of the mechanisms of thrombotic plaque erosion [J].
Durand, E ;
Scoazec, A ;
Lafont, A ;
Boddaert, J ;
Al Hajzen, A ;
Addad, F ;
Mirshahi, M ;
Desnos, M ;
Tedgui, A ;
Mallat, Z .
CIRCULATION, 2004, 109 (21) :2503-2506
[24]   A novel functional polymorphism in the PECAM-1 gene (53G>A) is associated with progression of atherosclerosis in the LOCAT and REGRESS studies [J].
Elrayess, MA ;
Webb, KE ;
Flavell, DM ;
Syvänne, M ;
Taskinen, MR ;
Frick, MH ;
Nieminen, MS ;
Kesäniemi, YA ;
Pasternack, A ;
Jukema, JW ;
Kastelein, JJP ;
Zwinderman, AH ;
Humphries, SE .
ATHEROSCLEROSIS, 2003, 168 (01) :131-138
[25]   Activin and TR3 orphan receptor: Two 'atheroprotective' genes as evidenced in dedicated mouse models [J].
Engelse, MA ;
Arkenbout, EK ;
Pannekoek, H ;
de Vries, CJ .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2003, 30 (11) :894-899
[26]   Adenoviral activin A expression prevents intimal hyperplasia in human and murine blood vessels by maintaining the contractile smooth muscle cell phenotype [J].
Engelse, MA ;
Lardenoye, JHP ;
Neele, JM ;
Grimbergen, JM ;
de Vries, MR ;
Lamfers, MLM ;
Pannekoek, H ;
Quax, PHA ;
de Vries, CJM .
CIRCULATION RESEARCH, 2002, 90 (10) :1128-1134
[27]   Molecular and biological properties of vascular endothelial growth factor [J].
Ferrara, N .
JOURNAL OF MOLECULAR MEDICINE-JMM, 1999, 77 (07) :527-543
[28]  
Fisslthaler B, 2000, ACTA PHYSIOL SCAND, V168, P81
[29]   Role of PECAM-1 in the shear-stress-induced activation of Akt and the endothelial nitric oxide synthase (eNOS) in endothelial cells [J].
Fleming, I ;
Fisslthaler, B ;
Dixit, M ;
Busse, R .
JOURNAL OF CELL SCIENCE, 2005, 118 (18) :4103-4111
[30]   Platelet endothelial cell adhesion molecule-1 and mechanotransduction in vascular endothelial cells [J].
Fujiwara, K .
JOURNAL OF INTERNAL MEDICINE, 2006, 259 (04) :373-380