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弓形虫可阻止由TLR触发的巨噬细胞活化所引发的染色质重塑。

Toxoplasma gondii prevents chromatin remodeling initiated by TLR-triggered macrophage activation.

作者信息

Leng Jin, Butcher Barbara A, Egan Charlotte E, Abi Abdallah Delbert S, Denkers Eric Y

机构信息

Department of Microbiology and Immunology, College of Veterinary Medicine, Cornell University, Ithaca, NY 14853, USA.

出版信息

J Immunol. 2009 Jan 1;182(1):489-97. doi: 10.4049/jimmunol.182.1.489.

Abstract

Macrophages infected with the opportunistic protozoan Toxoplasma gondii are unable to up-regulate many proinflammatory cytokine genes, including TNF (TNF-alpha), upon stimulation with LPS and other TLR ligands. In this study, we examined the influence of T. gondii on transcription factors associated with TNF-alpha transcription, as well as phosphorylation and acetylation of histone H3 at distal and proximal regions of the TNF-alpha promoter. During LPS stimulation, we found that Toxoplasma blocks nuclear accumulation of transcription factor c-Jun, but not that of cAMP response element-binding protein or NF-kappaB. However, chromatin immunoprecipitation studies revealed that binding of all of these transcription factors to the TNF promoter was decreased by T. gondii infection. Furthermore, the parasite blocked LPS-induced Ser(10) phosphorylation and Lys(9)/Lys(14) acetylation of histone H3 molecules associated with distal and proximal regions of the TNF-alpha promoter. Our results show that Toxoplasma inhibits TNF-alpha transcription by interfering with chromatin remodeling events required for transcriptional activation at the TNF promoter, revealing a new mechanism by which a eukaryotic pathogen incapacitates proinflammatory cytokine production during infection.

摘要

感染了机会性原生动物刚地弓形虫的巨噬细胞,在受到脂多糖(LPS)和其他Toll样受体(TLR)配体刺激时,无法上调包括肿瘤坏死因子(TNF-α)在内的许多促炎细胞因子基因。在本研究中,我们检测了弓形虫对与TNF-α转录相关的转录因子的影响,以及TNF-α启动子远端和近端区域组蛋白H3的磷酸化和乙酰化情况。在LPS刺激过程中,我们发现弓形虫会阻断转录因子c-Jun的核内积累,但不会阻断环磷酸腺苷反应元件结合蛋白(cAMP response element-binding protein)或核因子κB(NF-κB)的核内积累。然而,染色质免疫沉淀研究表明,弓形虫感染会降低所有这些转录因子与TNF启动子的结合。此外,该寄生虫还会阻断LPS诱导的与TNF-α启动子远端和近端区域相关的组蛋白H3分子的Ser(10)磷酸化和Lys(9)/Lys(14)乙酰化。我们的结果表明,弓形虫通过干扰TNF启动子转录激活所需的染色质重塑事件来抑制TNF-α转录,揭示了一种真核病原体在感染期间使促炎细胞因子产生失能的新机制。

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