Membrane-Anchored Serine Proteases in Health and Disease

被引:66
作者
Antalis, Toni M. [1 ]
Bugge, Thomas H. [2 ]
Wu, Qingyu [3 ]
机构
[1] Univ Maryland, Sch Med, Ctr Vasc & Inflammatory Dis, Baltimore, MD 21201 USA
[2] Natl Inst Dent & Craniofacial Res, Proteases & Tissue Remodeling Sect, Oral & Pharyngeal Canc Branch, NIH, Bethesda, MD USA
[3] Cleveland Clin, Lerner Res Inst NB20, Cleveland, OH 44106 USA
来源
PROTEASES IN HEALTH AND DISEASE | 2011年 / 99卷
关键词
HEPATOCYTE GROWTH-FACTOR; EPITHELIAL SODIUM-CHANNEL; TRYPSIN-LIKE PROTEASE; FACTOR ACTIVATOR INHIBITOR-1; AUTOSOMAL RECESSIVE ICHTHYOSIS; PROATRIAL NATRIURETIC PEPTIDE; PROSTATE-CANCER PROGRESSION; OVARIAN TUMOR-CELLS; INTESTINAL ENTEROKINASE DEFICIENCY; INFLUENZA-VIRUS HEMAGGLUTININ;
D O I
10.1016/S1877-1173(11)99001-2
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
Serine proteases of the trypsin-like family have long been recognized to be critical effectors of biological processes as diverse as digestion, blood coagulation, fibrinolysis, and immunity. In recent years, a subgroup of these enzymes has been identified that are anchored directly to plasma membranes, either by a carboxy-terminal transmembrane domain (Type I), an amino-terminal transmembrane domain with a cytoplasmic extension (Type II or TTSP), or through a glycosylphosphatidylinositol (GPI) linkage. Recent biochemical, cellular, and in vivo analyses have now established that membrane-anchored serine proteases are key pericellular contributors to processes vital for development and the maintenance of homeostasis. This chapter reviews our current knowledge of the biological and physiological functions of these proteases, their molecular substrates, and their contributions to disease.
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页码:1 / 50
页数:50
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