Fosang A J, Rogerson F M, East C J, Stanton H
University of Melbourne Department of Paediatrics and Murdoch Childrens Research Institute, Royal Children's Hospital, Parkville, Victoria, Australia.
Eur Cell Mater. 2008 Feb 5;15:11-26. doi: 10.22203/ecm.v015a02.
The recent discovery of ADAMTS-5 as the major aggrecanase in mouse cartilage came as a surprise. A great deal of research had focused on ADAMTS-4 and much less was known about the regulation, expression and activity of ADAMTS-5. Two years on, it is still not clear whether ADAMTS-4 or ADAMTS-5 is the major aggrecanase in human cartilage. On the one hand there are in vitro studies using siRNA, neutralising antibodies and immunoprecipitation with anti-ADAMTS antibodies that suggest a significant role for ADAMTS-4 in aggrecanolysis. On the other hand, ADAMTS-5 (but not ADAMTS-4)-deficient mice are protected from cartilage erosion in models of experimental arthritis, and recombinant human ADAMTS-5 is substantially more active than ADAMTS-4. The activity of both enzymes is modulated by C-terminal processing, which occurs naturally in vivo. The most interesting finding to emerge from our comparison of ADAMTS-5 and ADAMTS-4 is that in terms of gene regulation, these two enzymes are the antitheses of each other. In most cases, ADAMTS-5 is constitutively expressed in human chondrocytes and synovial fibroblasts, whereas ADAMTS-4 expression is induced by proinflammatory cytokines. This paper reviews the data on ADAMTS-5 so far. It represents a snapshot in time of a field that is fast-moving and very exciting.
最近发现ADAMTS-5是小鼠软骨中的主要聚糖酶,这一发现令人惊讶。此前大量研究都集中在ADAMTS-4上,而对ADAMTS-5的调节、表达和活性了解较少。两年过去了,ADAMTS-4还是ADAMTS-5是人类软骨中的主要聚糖酶仍不清楚。一方面,有使用小干扰RNA(siRNA)、中和抗体以及用抗ADAMTS抗体进行免疫沉淀的体外研究表明,ADAMTS-4在蛋白聚糖分解中起重要作用。另一方面,在实验性关节炎模型中,缺乏ADAMTS-5(而非ADAMTS-4)的小鼠可免受软骨侵蚀,并且重组人ADAMTS-5的活性明显高于ADAMTS-4。两种酶的活性都受C端加工的调节,这种加工在体内自然发生。我们对ADAMTS-5和ADAMTS-4进行比较时出现的最有趣的发现是,在基因调控方面,这两种酶彼此相反。在大多数情况下,ADAMTS-5在人软骨细胞和滑膜成纤维细胞中组成性表达,而ADAMTS-4的表达由促炎细胞因子诱导。本文综述了目前有关ADAMTS-5的数据。它代表了一个快速发展且非常令人兴奋的领域在某一时刻的情况。