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沙眼衣原体质粒编码蛋白 pORF5 通过 MAPK/ERK 信号通路激活未折叠蛋白反应诱导自噬。

Chlamydia trachomatis plasmid-encoded protein pORF5 activates unfolded protein response to induce autophagy via MAPK/ERK signaling pathway.

机构信息

Institute of Pathogenic Biology, Hengyang Medical College, Hunan Provincial Key Laboratory for Special Pathogens Prevention and Control, Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study, University of South China, Hengyang, 421001, PR China.

Institute of Pathogenic Biology, Hengyang Medical College, Hunan Provincial Key Laboratory for Special Pathogens Prevention and Control, Hunan Province Cooperative Innovation Center for Molecular Target New Drug Study, University of South China, Hengyang, 421001, PR China.

出版信息

Biochem Biophys Res Commun. 2020 Jun 30;527(3):805-810. doi: 10.1016/j.bbrc.2020.04.117. Epub 2020 May 20.

Abstract

Chlamydia trachomatis (C. trachomatis) is an obligate intracellular organism that depends on nutrients from the host cell for their replication and proliferation. Therefore, the interaction between this pathogen and host induces sustained endoplasmic reticulum (ER) stress in the infected cells. Unfolded protein response (UPR) has been demonstrated to be activated by chlamydial secreted effectors, allowing host cells to recover from the stressful state. In this study, we attempted to explore the role of the only secreted plasmid-encoded protein pORF5 of C. trachomatis between UPR and autophagy induction. The results showed that three branches of UPR (PERK, IRE1, and ATF6) were activated by pORF5. pORF5-induced autophagy was repressed by UPR inhibitors GSK2606414 and 4μ8C, while the autophagy inhibition was failed to influence pORF5-induced UPR significantly. MAPK/ERK inhibitor PD98059 partially suppressed the pORF5-induced autophagy, but had little effect on UPR, indicating that pORF5 actives UPR to induce autophagy via the MAPK/ERK signaling pathway. These observations provide clues on how the host maintains the cellular homeostasis during C. trachomatis infection.

摘要

沙眼衣原体(C. trachomatis)是一种专性细胞内病原体,其复制和增殖依赖于宿主细胞的营养物质。因此,该病原体与宿主之间的相互作用会导致感染细胞中持续的内质网(ER)应激。已证明未折叠蛋白反应(UPR)被衣原体分泌的效应物激活,使宿主细胞能够从应激状态中恢复。在这项研究中,我们试图探讨沙眼衣原体唯一分泌的质粒编码蛋白 pORF5 在 UPR 和自噬诱导之间的作用。结果表明,pORF5 激活了 UPR 的三条分支(PERK、IRE1 和 ATF6)。UPR 抑制剂 GSK2606414 和 4μ8C 抑制了 pORF5 诱导的自噬,而自噬抑制未能显著影响 pORF5 诱导的 UPR。MAPK/ERK 抑制剂 PD98059 部分抑制了 pORF5 诱导的自噬,但对 UPR 影响不大,表明 pORF5 通过 MAPK/ERK 信号通路激活 UPR 来诱导自噬。这些观察结果为宿主在沙眼衣原体感染过程中如何维持细胞内稳态提供了线索。

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