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Regulation of tumor necrosis factor-alpha and tumor necrosis factor converting enzyme in human osteoarthritis.

机译:人骨关节炎中肿瘤坏死因子-α和肿瘤坏死因子转化酶的调节。

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摘要

A snake venom-like protease isolated by a differential display screen between normal and osteoarthritis (OA)-affected cartilage (designated as cSVP) has a cDNA sequence identical to tumor necrosis factor (TNF)alpha convertase enzyme (TACE) and belongs to the adamalysin group of proteases. It has unique structural properties and when expressed in baculovirus, cleaves preferentially proTNFalpha to TNFalpha. The OA-affected cartilage has upregulated mRNA for TNFalpha and TACE as compared to normal cartilage. TNFalpha and TACE regulate inflammatory mediators in OA-affected cartilage which can be inhibited by both soluble TNFalpha receptors and inhibitors of TACE. These experiments demonstrate a functional paracrine/autocrine role of TNFalpha in OA-affected cartilage that is modulated by upregulated levels of chondrocyte-derived TACE. Copyright 1999 OsteoArthritis Research Society International.
机译:通过正常和骨关节炎(OA)受影响的软骨(称为cSVP)之间的差异显示屏幕分离出的蛇毒样蛋白酶,其cDNA序列与肿瘤坏死因子(TNF)α转化酶(TACE)相同,并且属于阿达马来霉素组蛋白酶。它具有独特的结构特性,当在杆状病毒中表达时,优先切割TNFα至TNFα。与正常软骨相比,受OA影响的软骨的TNFalpha和TACE mRNA上调。 TNFα和TACE调节受OA影响的软骨中的炎性介质,而可溶性TNFα受体和TACE抑制剂均可抑制它。这些实验证明了TNFα在OA影响的软骨中的功能性旁分泌/自分泌作用,其由软骨细胞衍生的TACE的上调水平调节。版权所有1999国际骨关节炎研究协会。

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