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首页> 外文期刊>Modern rheumatology >Correlation between MMP-13 and HDAC7 expression in human knee osteoarthritis.
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Correlation between MMP-13 and HDAC7 expression in human knee osteoarthritis.

机译:MMP-13和HDAC7在人膝骨关节炎中的表达之间的相关性。

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摘要

Recent studies suggest that histone deacetylase (HDAC) inhibitors may therapeutically prevent cartilage degradation in osteoarthritis (OA). Matrix metalloproteinase-13 (MMP-13) plays an important role in the pathogenesis of this disease and in the present study we investigated the correlation between HDACs and MMP-13. Comparing the expression of different HDACs in cartilage from OA patients and healthy donors, HDAC7 showed a significant elevation in cartilage from OA patients. High level of HDAC7 expression in OA cartilage was also confirmed by immunohistochemistry. Knockdown of HDAC7 by small interference RNA (siRNA) in SW1353 human chondrosarcoma cells strongly suppressed interleukin (IL)-1-dependent and independent induction of MMP-13 gene expression. In conclusion, elevated HDAC7 expression in human OA may contribute to cartilage degradation via promoting MMP-13 gene expression, suggesting the critical role of MMP-13 in OA pathogenesis.
机译:最近的研究表明,组蛋白脱乙酰基酶(HDAC)抑制剂可治疗性预防骨关节炎(OA)中的软骨降解。基质金属蛋白酶-13(MMP-13)在这种疾病的发病机理中起着重要作用,在本研究中,我们研究了HDAC和MMP-13之间的相关性。比较OA患者和健康供体软骨中不同HDAC的表达,HDAC7显示OA患者软骨显着升高。免疫组织化学也证实了OA软骨中HDAC7的高表达。在SW1353人软骨肉瘤细胞中通过小干扰RNA(siRNA)敲低HDAC7可以强烈抑制白介素(IL)-1依赖性和独立诱导的MMP-13基因表达。总之,人类OA中HDAC7表达的升高可能通过促进MMP-13基因表达来促进软骨的降解,提示MMP-13在OA发病机理中的关键作用。

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