Granule-associated serine proteases: granzymes might not just be killer proteases

被引:69
作者
Froelich, Christopher J. [1 ]
Pardo, Julian [2 ]
Simon, Markus M. [3 ]
机构
[1] Northshore Univ, Healthsyst Res Inst, Dept Med, Evanston, IL 60201 USA
[2] Univ Zaragoza, Dept Biochem & Mol & Cellular Biol, Fac Sci, Fdn Aragon 1D, Zaragoza 50009, Spain
[3] Max Planck Inst Immunobiol, Metschnikoff Lab, D-79108 Freiburg, Germany
关键词
CYTOLYTIC LYMPHOCYTES-T; INDEPENDENT CELL-DEATH; RHEUMATOID-ARTHRITIS; CASPASE ACTIVATION; TARGET-CELLS; IN-VITRO; EXTRACELLULAR ACTIVITIES; MEDIATED CYTOTOXICITY; CYTOCHROME-C; INFECTION;
D O I
10.1016/j.it.2009.01.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
The cytotoxic cell granule secretory pathway is viewed as indispensable for eliminating tumor and virally infected cells through a process in which the pore-forming protein, perforin, delivers the serine protease granzymes into cells targeted for destruction. Residing in cytotoxic cells, granzymes were originally anticipated to act both extracellularly and intracellularly. With the discovery that isolated granzymes induce apoptosis when combined with perforin, the broader functionality of the granzymes became unattractive. The purpose of this article is to describe observations indicating that granzymes possess non-cytotoxic activities that might include such diverse biologic effects as stimulation of pro-inflammatory cytokines, remodeling of extracellular matrices and inactivation of intracellular pathogens.
引用
收藏
页码:117 / 123
页数:7
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