Dai Hongyan, Korthuis Ronald J
Department of Medical Pharmacology and Physiology and Dalton Cardiovascular Research Center, University of Missouri, School of Medicine, Columbia, Missouri 65212.
Drug Discov Today Dis Models. 2011 Spring;8(1):47-55. doi: 10.1016/j.ddmod.2011.06.004.
Mast cells are best known for their role in allergic reactions but are also now recognized for their important contributions to a number of disparate inflammatory conditions through the release of inflammatory mediators, serglycin and other proteoglycans, and proteases. Because these tissue resident inflammatory cells express proteases in such great abundance and their enzymatic activity results in cleavage of a multitude of proteins and peptides, which in turn modify tissue function, their substrate specificity, tissue distribution, and mode of action have become the subjects of great interest. Although mast cell protease-dependent proteolysis is critical to host defense against invading pathogens, regulation of these hydrolytic enzymes is essential to limiting self-induced damage as well. Indeed, dysregulated release of mast cell proteases is now recognized to contribute to the pathogenesis of a number of inflammatory conditions including asthma, abdominal aortic aneurysm formation, vessel damage in atherosclerosis and hypertension, arthritis, and ischemia/reperfusion injury. Understanding how mast cell proteases contribute to inflammation will thus help unravel molecular mechanisms that underlie such immunologic disorders and will help identify new therapeutic targets for drug development.
肥大细胞因其在过敏反应中的作用而最为人所知,但现在也因其通过释放炎症介质、丝甘蛋白聚糖和其他蛋白聚糖以及蛋白酶,对多种不同的炎症性疾病做出重要贡献而受到认可。由于这些组织驻留的炎症细胞大量表达蛋白酶,且其酶活性导致多种蛋白质和肽的裂解,进而改变组织功能,因此它们的底物特异性、组织分布和作用方式已成为人们极大关注的课题。尽管肥大细胞蛋白酶依赖性蛋白水解对于宿主抵御入侵病原体至关重要,但对这些水解酶的调节对于限制自身诱导的损伤也必不可少。事实上,现在人们认识到肥大细胞蛋白酶的释放失调会导致多种炎症性疾病的发病机制,包括哮喘、腹主动脉瘤形成、动脉粥样硬化和高血压中的血管损伤、关节炎以及缺血/再灌注损伤。因此,了解肥大细胞蛋白酶如何促进炎症将有助于揭示这些免疫性疾病背后的分子机制,并有助于确定药物开发的新治疗靶点。