白细胞介素-10在LPS耐受中上调。

Journal of inflammation Pub Date : 1995-01-01
M Frankenberger, H Pechumer, H W Ziegler-Heitbrock
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引用次数: 0

摘要

脂多糖(LPS)刺激人单核细胞系Mono Mac 6可导致促炎细胞因子肿瘤坏死因子(TNF)和抗炎细胞因子白介素-10 (IL-10)的快速表达。将这些细胞用低剂量LPS预培养2天,使细胞能够耐受随后的刺激,因为TNF基因在mRNA和蛋白质水平上的表达都很低。然而,IL-10表现出一种互惠模式,因为该基因的表达在预培养细胞中上调,并且在随后的刺激下会进一步增加。虽然TNF已被证明可以诱导IL-10,并且IL-10被发现下调TNF,但这种相互调节并不能解释Mono Mac 6中观察到的LPS耐受模式,因为针对TNF和IL-10的中和抗体不能分别阻止IL-10的上调和TNF的下调。然而,在LPS预培养期间用干扰素- γ (ifn - γ)处理Mono Mac 6细胞可以逆转耐受:LPS/ ifn - γ预培养的细胞在随后的刺激下产生高水平的TNF转录本,而IL-10基因的反应减弱。数据显示,LPS耐受并不涉及所有类型单核细胞功能的被动下调,但它是一种与抗炎细胞因子的下调和上调相协调的反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Interleukin-10 is upregulated in LPS tolerance.

Lipopolysaccharide (LPS) stimulation of the human monocytic cell line Mono Mac 6 leads to rapid expression of both the pro-inflammatory cytokine tumor necrosis factor (TNF) and the anti-inflammatory cytokine interleukin-10 (IL-10). Preculture of these cells with a low dose of LPS for 2 days rendered the cells tolerant to subsequent stimulation, in that TNF gene expression is only minimal, both at the mRNA and at the protein level. IL-10 shows a reciprocal pattern, however, as expression of this gene is upregulated in precultured cells, and it will further increase upon subsequent stimulation. Although TNF has been shown to induce IL-10, and IL-10 was found to downregulate TNF, this reciprocal regulation does not explain the pattern observed in LPS tolerance in Mono Mac 6, since neutralizing antibodies against TNF and IL-10 could not prevent upregulation of IL-10 and downregulation of TNF, respectively. Treatment of Mono Mac 6 cells during LPS preculture with interferon-gamma (IFN-gamma) could, however, reverse tolerance: LPS/IFN-gamma precultured cells produced high levels of TNF transcripts upon subsequent stimulation, while the response of the IL-10 gene was attenuated. The data show that LPS tolerance does not involve a passive downregulation of all types of monocyte functions, but it is an orchestrated response with downregulation of pro- and upregulation of anti-inflammatory cytokines.

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