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The ADAMTS (A Disintegrin and Metalloproteinase with Thrombospondin motifs) family

机译:ADAMTS(具有血小板反应蛋白基序的整合素和金属蛋白酶)家族

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摘要

The ADAMTS (A Disintegrin and Metalloproteinase with Thrombospondin motifs) enzymes are secreted, multi-domain matrix-associated zinc metalloendopeptidases that have diverse roles in tissue morphogenesis and patho-physiological remodeling, in inflammation and in vascular biology. The human family includes 19 members that can be sub-grouped on the basis of their known substrates, namely the aggrecanases or proteoglycanases (ADAMTS1, 4, 5, 8, 9, 15 and 20), the procollagen N-propeptidases (ADAMTS2, 3 and 14), the cartilage oligomeric matrix protein-cleaving enzymes (ADAMTS7 and 12), the von-Willebrand Factor proteinase (ADAMTS13) and a group of orphan enzymes (ADAMTS6, 10, 16, 17, 18 and 19). Control of the structure and function of the extracellular matrix (ECM) is a central theme of the biology of the ADAMTS, as exemplified by the actions of the procollagen-N-propeptidases in collagen fibril assembly and of the aggrecanases in the cleavage or modification of ECM proteoglycans. Defects in certain family members give rise to inherited genetic disorders, while the aberrant expression or function of others is associated with arthritis, cancer and cardiovascular disease. In particular, ADAMTS4 and 5 have emerged as therapeutic targets in arthritis. Multiple ADAMTSs from different sub-groupings exert either positive or negative effects on tumorigenesis and metastasis, with both metalloproteinase-dependent and -independent actions known to occur. The basic ADAMTS structure comprises a metalloproteinase catalytic domain and a carboxy-terminal ancillary domain, the latter determining substrate specificity and the localization of the protease and its interaction partners; ancillary domains probably also have independent biological functions. Focusing primarily on the aggrecanases and proteoglycanases, this review provides a perspective on the evolution of the ADAMTS family, their links with developmental and disease mechanisms, and key questions for the future.
机译:ADAMTS(具有血小板反应蛋白基序的整合素和金属蛋白酶)酶是分泌的,多域基质相关的锌金属内肽酶,在组织形态发生和病理生理重塑,炎症和血管生物学中具有多种作用。人类家族包括19个成员,这些成员可以根据它们的已知底物进行分组,即聚集蛋白聚糖酶或蛋白聚糖酶(ADAMTS1、4、5、8、9、15和20),胶原蛋白N-前肽酶(ADAMTS2、3) 14),软骨寡聚基质蛋白裂解酶(ADAMTS7和12),冯-威勒布兰德因子蛋白酶(ADAMTS13)和一组孤儿酶(ADAMTS6、10、16、17、18和19)。控制细胞外基质(ECM)的结构和功能是ADAMTS生物学的中心主题,例如胶原蛋白原纤维中前胶原蛋白N-前肽酶的作用以及胶原蛋白的切割或修饰中的聚集蛋白聚糖酶的作用。 ECM蛋白聚糖。某些家庭成员的缺陷会导致遗传性遗传疾病,而其他家庭成员的异常表达或功能则与关节炎,癌症和心血管疾病有关。特别地,ADAMTS4和5已经成为关节炎的治疗靶标。来自不同亚组的多个ADAMTS对肿瘤发生和转移产生正向或负向影响,已知会发生金属蛋白酶依赖性和非依赖性作用。基本的ADAMTS结构包括金属蛋白酶催化结构域和羧基末端辅助结构域,后者决定底物特异性和蛋白酶及其相互作用伙伴的定位。辅助结构域也可能具有独立的生物学功能。本文主要针对聚集蛋白聚糖酶和蛋白聚糖酶,对ADAMTS家族的进化,它们与发育和疾病机制的联系以及未来的关键问题提供了一个观点。

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