Proteinase-activated receptor 1 (PAR-1) and cell apoptosis

被引:64
作者
Flynn, AN
Buret, AG
机构
[1] Univ Calgary, Dept Biol Sci, Calgary, AB T2N 1N4, Canada
[2] Univ Calgary, Mucosal Inflammat Res Grp, Calgary, AB T2N 1N4, Canada
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
apoptosis; epithelial cells; microbial proteinases; myosin light chain; proteinase-activated recepter 1;
D O I
10.1023/B:APPT.0000045784.49886.96
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
This review summarizes the main aspects and newest findings of how proteinase-activated receptor 1 (PAR-1) may modulate programmed cell death. Activation of PAR-1 has been found to induce or inhibit apoptosis in a variety of cells, depending on the dosage of its physiological agonist thrombin, or that of synthetic receptor activators. To date, cellular targets for PAR-1-mediated effects on apoptosis include neuronal, endothelial, and epithelial cells, fibroblasts, and tumor cells. The signaling pathways involved in the induction or prevention of apoptosis by PAR-1 activation are diverse, and include JAK/STAT, RhoA, myosin light chain kinase, ERK1/2, and various Bcl-2 family members. In view of the well-established involvement of microbial proteinases in host tissue malfunction, the article also elaborates on the possible significance of PAR-1 activation for the pathogenesis of infectious disease.
引用
收藏
页码:729 / 737
页数:9
相关论文
共 92 条
[51]   Intestinal epithelial cell apoptosis following Cryptosporidium parvum infection [J].
McCole, DF ;
Eckmann, L ;
Laurent, F ;
Kagnoff, MF .
INFECTION AND IMMUNITY, 2000, 68 (03) :1710-1713
[52]   THROMBIN STIMULATES PROLIFERATION OF CULTURED RAT AORTIC SMOOTH-MUSCLE CELLS BY A PROTEOLYTICALLY ACTIVATED RECEPTOR [J].
MCNAMARA, CA ;
SAREMBOCK, IJ ;
GIMPLE, LW ;
FENTON, JW ;
COUGHLIN, SR ;
OWENS, GK .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (01) :94-98
[53]   Streptokinase-induced platelet activation involves antistreptokinase antibodies and cleavage of protease-activated receptor-1 [J].
McRedmond, JP ;
Harriott, P ;
Walker, B ;
Fitzgerald, DJ .
BLOOD, 2000, 95 (04) :1301-1308
[54]   Thrombin activates two stress-activated protein kinases, c-Jun N-terminal kinase and p38, in HepG2 cells [J].
Mitsui, H ;
Maruyama, T ;
Kimura, S ;
Takuwa, Y .
HEPATOLOGY, 1998, 27 (05) :1362-1367
[55]   Thrombin receptor activation elicits rapid protein tyrosine phosphorylation and stimulation of the Raf-1/MAP kinase pathway preceding delayed mitogenesis in cultured rat aortic smooth muscle cells - Evidence for an obligate autocrine mechanism promoting cell proliferation induced by G protein-coupled receptor agonists [J].
Molloy, CJ ;
Pawlowski, JE ;
Taylor, DS ;
Turner, CE ;
Weber, H ;
Peluso, M ;
Seiler, SM .
JOURNAL OF CLINICAL INVESTIGATION, 1996, 97 (05) :1173-1183
[56]   Entamoeba histolytica cysteine proteinases disrupt the polymeric structure of colonic mucin and alter its protective function [J].
Moncada, D ;
Keller, K ;
Chadee, K .
INFECTION AND IMMUNITY, 2003, 71 (02) :838-844
[57]   Inhibition of staurosporine-induced apoptosis of endothelial cells by activated protein C requires protease-activated receptor-1 and endothelial cell protein C receptor [J].
Mosnier, LO ;
Griffin, JH .
BIOCHEMICAL JOURNAL, 2003, 373 :65-70
[58]   RhoA- and RhoD-dependent regulatory switch of Gα subunit signaling by PAR-1 receptors in cellular invasion [J].
Nguyen, QD ;
Faivre, S ;
Bruyneel, E ;
Rivat, C ;
Seto, M ;
Endo, T ;
Mareel, M ;
Emami, S ;
Gespach, C .
FASEB JOURNAL, 2002, 16 (06) :565-576
[59]   Protease-activated receptor 1 (PAR-1) is required and rate-limiting for thrombin-enhanced experimental pulmonary metastasis [J].
Nierodzik, ML ;
Chen, K ;
Takeshita, K ;
Li, JJ ;
Huang, YQ ;
Feng, XS ;
D'Andrea, MR ;
Andrade-Gordon, P ;
Karpatkin, S .
BLOOD, 1998, 92 (10) :3694-3700
[60]  
NIERODZIK MLR, 1992, CANCER RES, V52, P3267