首页> 外文期刊>The Biochemical Journal >Cloning of the gene for interstitial collagenase-3 (matrix metalloproteinase-13) from rabbit synovial fibroblasts: differential expression with collagenase-1 (matrix metalloproteinase-1)
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Cloning of the gene for interstitial collagenase-3 (matrix metalloproteinase-13) from rabbit synovial fibroblasts: differential expression with collagenase-1 (matrix metalloproteinase-1)

机译:兔滑膜成纤维细胞间质胶原酶-3(基质金属蛋白酶-13)基因的克隆:胶原酶-1(基质金属蛋白酶-1)的差异表达

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摘要

Cartilage, bone and the interstitial stroma, composed largely of the interstitial collagens, types I, II and III, are remodelled by three members of the metalloproteinase (MMP) family, collagenase-1 (MMP-1), collagenase-2 (MMP-8) and collagenase-3 (MMP-13). MMP-1 and MMP-13 may contribute directly to disease progression, since they are induced in patients with rheumatoid arthritis and osteoarthritis. The study of MMP-1 and MMP-13 gene regulation in models of arthritic disease has been problematic because mice and rats, which are typically used, only possess a homologue of MMP-13. Here we show that in contrast with mice and rats, rabbits possess distinct genes homologous to human MMP-1 and MMP-13. Furthermore, rabbit MMP-13 is expressed simultaneously with MMP-1 in chondrocytes and synovial fibroblasts in response to the cytokines interleukin-1 and tumour necrosis factor-alpha, or the phorbol ester PMA. The time course of MMP-13 induction is more rapid and transient than that of MMP-1, suggesting that distinct mechanisms regulate the expression of these two collagenases. We have cloned the rabbit MMP-13 gene from synovial fibroblasts and demonstrated that the rabbit gene shares greater homology with human MMP-13 than does the mouse interstitial collagenase. Together with the fact that mice and rats do not possess a homologue to human MMP-1, our data suggest that the rabbit provides an appropriate model for studying the roles of interstitial collagenases in connective-tissue diseases, such as rheumatoid arthritis and osteoarthritis. [References: 36]
机译:软骨,骨骼和间质基质主要由I型,II型和III型间质胶原组成,由金属蛋白酶(MMP)家族的三个成员,胶原酶1(MMP-1),胶原酶2(MMP- 8)和胶原酶3(MMP-13)。 MMP-1和MMP-13可能直接导致疾病进展,因为它们是在类风湿关节炎和骨关节炎患者中诱发的。在关节炎疾病模型中对MMP-1和MMP-13基因调控的研究存在问题,因为通常使用的小鼠和大鼠仅具有MMP-13的同源物。在这里,我们显示与小鼠和大鼠相反,兔子拥有与人MMP-1和MMP-13同源的独特基因。此外,响应细胞因子白细胞介素-1和肿瘤坏死因子-α或佛波酯PMA,兔MMP-13在软骨细胞和滑膜成纤维细胞中与MMP-1同时表达。 MMP-13诱导的时间过程比MMP-1诱导的过程更迅速和更短暂,表明不同的机制调节着这两种胶原酶的表达。我们已经从滑膜成纤维细胞克隆了兔MMP-13基因,并证明了该兔基因与人MMP-13的同源性比小鼠间质胶原酶更大。结合小鼠和大鼠不具有人类MMP-1同源物这一事实,我们的数据表明,兔子为研究间质胶原酶在结缔组织疾病(如类风湿性关节炎和骨关节炎)中的作用提供了合适的模型。 [参考:36]

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