Clarke C J, Taylor-Fishwick D A, Hales A, Chernajovsky Y, Sugamura K, Feldmann M, Foxwell B M
Kennedy Institute of Rheumatology, Sunley Division, London, Great Britain.
Eur J Immunol. 1995 Oct;25(10):2961-6. doi: 10.1002/eji.1830251037.
The murine pre-B cell line 70Z/3 responds to lipopolysaccharide by up-regulating the surface expression of kappa (kappa) light chain through activation of the transcription factor NF kappa B. Interleukin-4 (IL-4), a T cell cytokine, is a known inhibitor of some LPS-mediated events. We investigated whether IL-4 could inhibit the up-regulation of kappa light chain and activation of NF kappa B by LPS in 70Z/3. IL-4 partially inhibited both the LPS-induced expression of kappa light chain and also the activation of NF kappa B as judged by an NF kappa B reporter gene assay. Additionally, electrophoretic mobility shift assays confirmed this effect on LPS-induced NF kappa B DNA binding activity in the nucleus. Surprisingly, proteolytic degradation of I kappa B alpha (MAD3), a prerequisite for NF kappa B activation, was unaffected by IL-4, implying that this cytokine inhibits some subsequent undefined event in the activation of NF kappa B. IL-4 was also found partially to inhibit NF kappa B activity induced by tumor necrosis factor-alpha (TNF-alpha) and interleukin-1-beta (IL-1 beta). These results indicate that there may be a common mechanism for the well-documented anti-inflammatory effects of IL-4 and that this mechanism involves the transcription factor NF kappa B.
小鼠前B细胞系70Z/3通过激活转录因子NF-κB上调κ轻链的表面表达来响应脂多糖。白细胞介素-4(IL-4)是一种T细胞细胞因子,是某些LPS介导事件的已知抑制剂。我们研究了IL-4是否能抑制70Z/3中LPS诱导的κ轻链上调和NF-κB激活。通过NF-κB报告基因测定判断,IL-4部分抑制了LPS诱导的κ轻链表达以及NF-κB激活。此外,电泳迁移率变动分析证实了对LPS诱导的细胞核中NF-κB DNA结合活性的这种作用。令人惊讶的是,NF-κB激活的先决条件IκBα(MAD3)的蛋白水解降解不受IL-4影响,这意味着这种细胞因子抑制了NF-κB激活中一些随后未明确的事件。还发现IL-4部分抑制肿瘤坏死因子-α(TNF-α)和白细胞介素-1-β(IL-1β)诱导的NF-κB活性。这些结果表明,IL-4具有充分记录的抗炎作用可能存在共同机制,并且该机制涉及转录因子NF-κB。