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ADAMTS5 is the major aggrecanase in mouse cartilage in vivo and in vitro

机译:ADAMTS5是体内和体外小鼠软骨中的主要聚集蛋白聚糖酶

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Aggrecan is the major proteoglycan in cartilage, endowing this tissue with the unique capacity to bear load and resist compression. In arthritic cartilage, aggrecan is degraded by one or more 'aggrecanases' from the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs') family of proteinases. ADAMTS1, 8 and 9 have weak aggrecan-degrading activity. However, they are not thought to be the primary aggrecanases because ADAMTS1 null mice are not protected from experimental arthritis, and cleavage by ADAMTS8 and 9 is highly inefficient. Although ADAMTS4 and 5 are expressed in joint tissues, and are known to be efficient aggrecanases in vitro, the exact contribution of these two enzymes to cartilage pathology is unknown. Here we show that ADAMTS5 is the major aggrecanase in mouse cartilage, both in vitro and in a mouse model of inflammatory arthritis. Our data suggest that ADAMTS5 may be a suitable target for the development of new drugs designed to inhibit cartilage destruction in arthritis, although further work will be required to determine whether ADAMTS5 is also the major aggrecanase in human arthritis.
机译:Aggrecan是软骨中的主要蛋白聚糖,赋予该组织独特的承载力和抗压能力。在关节炎的软骨中,聚集蛋白聚糖被ADAMTS(具有血小板反应蛋白基序的整联蛋白和金属蛋白酶)家族的一种或多种“ aggrecanases”降解。 ADAMTS1、8和9具有弱的聚集蛋白聚糖降解活性。但是,它们不被认为是主要的软骨聚集蛋白聚糖酶,因为ADAMTS1缺失小鼠没有受到实验性关节炎的保护,而ADAMTS8和9的切割效率非常低。尽管ADAMTS4和5在关节组织中表达,并且在体外已知是有效的软骨聚集蛋白聚糖酶,但这两种酶对软骨病理的确切贡献尚不清楚。在这里,我们显示ADAMTS5是小鼠软骨的主要软骨聚集蛋白聚糖酶,无论是在体外还是在炎症性关节炎小鼠模型中。我们的数据表明,ADAMTS5可能是开发旨在抑制关节炎中的软骨破坏的新药的合适靶标,尽管还需要进一步的工作来确定ADAMTS5是否也是人类关节炎中的主要软骨聚集蛋白聚糖酶。

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