Bondeson J, Brennan F, Foxwell B, Feldmann M
Kennedy Institute of Rheumatology, London, UK.
J Rheumatol. 2000 Sep;27(9):2078-89.
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).
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.
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.
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.
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)。
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。
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。
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。