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Toxoplasma gondii Inhibits Covalent Modification of Histone H3 at the IL-10 Promoter in Infected Macrophages

机译:弓形虫在感染的巨噬细胞中抑制IL-10启动子上组蛋白H3的共价修饰

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摘要

Infection of macrophages with the protozoan parasite Toxoplasma gondii results in inhibition of a large panel of LPS-responsive cytokines, including TNF-α, while leaving others such as IL-10 intact. Recent studies provide evidence that the parasite interferes with chromatin remodeling at the TNF-α promoter that is normally associated with LPS stimulation, but that is not required for TLR4 induction of IL-10. Here, we examined the effect of Toxoplasma on IL-10 induced by simultaneous signaling through TLR4 and FcγR, a combined stimulus that triggers histone H3 covalent modification at the IL-10 promoter resulting in high level IL-10 cytokine production. We show that the parasite inhibits high level IL-10 production and prevents histone H3 Ser10 phosphorylation and Lys9/14 acetylation at the IL-10 promoter. These results provide compelling evidence that T. gondii targets the host cell chromatin remodeling machinery to down-regulate cytokine responses in infected macrophages.
机译:巨噬细胞感染了原生动物的弓形虫弓形虫会抑制大量LPS反应性细胞因子(包括TNF-α),而其他诸如IL-10的细胞则保持完整。最近的研究提供了证据,该寄生虫干扰了通常与LPS刺激相关的TNF-α启动子上的染色质重塑,但这不是TLR4诱导IL-10所必需的。在这里,我们检查了弓形虫对通过TLR4和FcγR同时发信号诱导的IL-10的影响,这是一种联合刺激,在IL-10启动子处触发组蛋白H3共价修饰,导致高水平的IL-10细胞因子产生。我们显示该寄生虫抑制高水平的IL-10产生,并阻止IL-10启动子处的组蛋白H3 Ser 10 磷酸化和Lys 9/14 乙酰化。这些结果提供了令人信服的证据,表明弓形虫靶向宿主细胞染色质重塑机制以下调感染的巨噬细胞中的细胞因子应答。

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