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
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