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抑瘤素M对人关节软骨中TIMP - 1生成的刺激作用。

Stimulation of TIMP-1 production by oncostatin M in human articular cartilage.

作者信息

Nemoto O, Yamada H, Mukaida M, Shimmei M

机构信息

National Defense Medical College, Saitama, Japan.

出版信息

Arthritis Rheum. 1996 Apr;39(4):560-6. doi: 10.1002/art.1780390404.

Abstract

OBJECTIVE

To investigate the effects of the interleukin-6 (IL-6) family cytokines, such as IL-6, IL-11, leukemia inhibitory factor (LIF), and oncostatin M (OSM), on the production of tissue inhibitor of matrix metalloproteinases 1 (TIMP-1) in human articular cartilage.

METHODS

Effects of IL-6 family cytokines and growth factors on TIMP-1 production were studied in human articular chondrocytes, grown as monolayer and cartilage explant culture. TIMP-1 protein levels in the cultured medium were measured by sandwich enzyme immunoassay. TIMP-1 messenger RNA levels in the cultured chondrocytes were analyzed by Northern blotting. Western blot analysis was performed to evaluate the release of matrix metalloproteinases (MMPs) in the cultured medium. Cell proliferation of chondrocytes was determined by 3H-thymidine uptake.

RESULTS

IL-6 family cytokines induced TIMP-1 expression in monolayer and explant culture, and the production of TIMP-1 was most stimulated by OSM. In contrast, OSM did not modulate the release of MMPs and cell proliferation.

CONCLUSION

These results suggest that OSM may be characterized as one of the chondroprotective mediators in cartilage destruction.

摘要

目的

研究白细胞介素-6(IL-6)家族细胞因子,如IL-6、IL-11、白血病抑制因子(LIF)和抑瘤素M(OSM),对人关节软骨中基质金属蛋白酶组织抑制因子1(TIMP-1)产生的影响。

方法

在单层培养和软骨外植体培养的人关节软骨细胞中,研究IL-6家族细胞因子和生长因子对TIMP-1产生的影响。通过夹心酶免疫测定法测量培养基中TIMP-1蛋白水平。通过Northern印迹分析培养的软骨细胞中TIMP-1信使核糖核酸水平。进行蛋白质印迹分析以评估培养基中基质金属蛋白酶(MMPs)的释放。通过3H-胸腺嘧啶核苷摄取测定软骨细胞的增殖。

结果

IL-6家族细胞因子在单层培养和外植体培养中诱导TIMP-1表达,且TIMP-1的产生受OSM刺激最大。相比之下,OSM不调节MMPs的释放和细胞增殖。

结论

这些结果表明,OSM可能是软骨破坏中软骨保护介质之一。

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