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将IkappaBalpha有效腺病毒转移至人成纤维细胞和软骨肉瘤细胞表明,基质金属蛋白酶和促炎细胞因子的诱导是核因子-κB依赖性的。

Effective adenoviral transfer of IkappaBalpha into human fibroblasts and chondrosarcoma cells reveals that the induction of matrix metalloproteinases and proinflammatory cytokines is nuclear factor-kappaB dependent.

作者信息

Bondeson J, Brennan F, Foxwell B, Feldmann M

机构信息

Kennedy Institute of Rheumatology, London, UK.

出版信息

J Rheumatol. 2000 Sep;27(9):2078-89.

Abstract

OBJECTIVE

To determine whether, in human fibroblasts and chondrosarcoma cells, the regulation of interleukins (IL)-6, 8, and 11 and matrix metalloproteinases (MMP)-1, 3, and 13, and their tissue inhibitor TIMP-1, depends on the transcription factor nuclear factor-kappaB (NF-kappaB).

METHODS

Fibroblasts and chondrosarcoma cells were effectively infected with an adenovirus encoding human IkappaBalpha, and inhibition of NF-kappaB function was observed. The induction of MMP and IL-6, 8, and 11 by various stimuli was assessed by ELISA.

RESULTS

The induction of IL-6 and IL-8 clearly depended on NF-kappaB in both fibroblasts and chondrosarcoma cells, irrespective of stimulus, but IkappaBalpha overexpression had little effect on IL-11. MMP-1, -3, and -13 were also inhibited, but TIMP-1 was unaffected.

CONCLUSION

NF-kappaB appears to play an important and selective role in MMP induction in human fibroblasts and chondrosarcoma cells. This suggests there are NF-kappaB dependent mechanisms of cartilage destruction in rheumatoid arthritis, and supports the concept that there are similarities in the regulation of inflammatory and destructive pathways in that disease.

摘要

目的

确定在人成纤维细胞和软骨肉瘤细胞中,白细胞介素(IL)-6、8和11以及基质金属蛋白酶(MMP)-1、3和13及其组织抑制剂TIMP-1的调节是否依赖于转录因子核因子-κB(NF-κB)。

方法

用编码人IκBα的腺病毒有效感染成纤维细胞和软骨肉瘤细胞,观察NF-κB功能的抑制情况。通过酶联免疫吸附测定法评估各种刺激对MMP以及IL-6、8和11的诱导作用。

结果

在成纤维细胞和软骨肉瘤细胞中,IL-6和IL-8的诱导明显依赖于NF-κB,与刺激无关,但IκBα的过表达对IL-11影响很小。MMP-1、-3和-13也受到抑制,但TIMP-1未受影响。

结论

NF-κB似乎在人成纤维细胞和软骨肉瘤细胞的MMP诱导中起重要的选择性作用。这表明类风湿性关节炎中存在依赖NF-κB的软骨破坏机制,并支持该疾病炎症和破坏途径调节存在相似性的概念。

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