Murphy Gillian, Knäuper Vera, Atkinson Susan, Butler George, English William, Hutton Mike, Stracke Jan, Clark Ian
School of Biological Sciences, University of East Anglia, Norwich, UK.
Arthritis Res. 2002;4 Suppl 3(Suppl 3):S39-49. doi: 10.1186/ar572. Epub 2002 May 9.
The role of matrix metalloproteinases in the degradative events invoked in the cartilage and bone of arthritic joints has long been appreciated and attempts at the development of proteinase inhibitors as potential therapeutic agents have been made. However, the spectrum of these enzymes orchestrating connective tissue turnover and general biology is much larger than anticipated. Biochemical studies of the individual members of the matrix metalloproteinase family are now underway, ultimately leading to a more detailed understanding of the function of their domain structures and to defining their specific role in cellular systems and the way that they are regulated. Coupled with a more comprehensive and detailed study of proteinase expression in different cells of joint tissues during the progress of arthritic diseases, it will be possible for the future development and application of highly specific proteinase inhibitors to be directed at specific key cellular events.
基质金属蛋白酶在关节炎关节软骨和骨中引发的降解过程中的作用早已为人所知,并且人们已尝试开发蛋白酶抑制剂作为潜在治疗药物。然而,这些协调结缔组织更新和一般生物学过程的酶的范围比预期的要大得多。目前正在对基质金属蛋白酶家族的各个成员进行生化研究,最终将更详细地了解其结构域功能,并确定它们在细胞系统中的特定作用以及调节方式。结合对关节炎疾病进展过程中关节组织不同细胞中蛋白酶表达的更全面、详细的研究,未来有可能针对特定关键细胞事件开发和应用高度特异性的蛋白酶抑制剂。