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首页> 外文期刊>Progress in Artificial Intelligence >Pathogens MenTORing Macrophages and Dendritic Cells: Manipulation of mTOR and Cellular Metabolism to Promote Immune Escape
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Pathogens MenTORing Macrophages and Dendritic Cells: Manipulation of mTOR and Cellular Metabolism to Promote Immune Escape

机译:病原体染色巨噬细胞和树突细胞:MTOR和细胞代谢的操纵,促进免疫逃逸

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摘要

Myeloid cells, including macrophages and dendritic cells, represent an important first line of defense against infections. Upon recognition of pathogens, these cells undergo a metabolic reprogramming that supports their activation and ability to respond to the invading pathogens. An important metabolic regulator of these cells is mammalian target of rapamycin (mTOR). During infection, pathogens use host metabolic pathways to scavenge host nutrients, as well as target metabolic pathways for subversion of the host immune response that together facilitate pathogen survival. Given the pivotal role of mTOR in controlling metabolism and DC and macrophage function, pathogens have evolved strategies to target this pathway to manipulate these cells. This review seeks to discuss the most recent insights into how pathogens target DC and macrophage metabolism to subvert potential deleterious immune responses against them, by focusing on the metabolic pathways that are known to regulate and to be regulated by mTOR signaling including amino acid, lipid and carbohydrate metabolism, and autophagy.
机译:骨髓细胞(包括巨噬细胞和树突状细胞)代表了对感染的重要第一道防线。在识别病原体后,这些细胞经历了一种代谢重编程,支持其激活和响应入侵病原体的能力。这些细胞的重要代谢调节剂是哺乳动物雷帕霉素(MTOR)的靶标。在感染期间,病原体使用宿主代谢途径来清除宿主营养素,以及针对宿主免疫应答的颠覆宿主的靶代谢途径,其共同促进病原体存活。鉴于MTOR在控制代谢和DC和巨噬细胞功能方面的关键作用,病原体具有靶向该途径以操纵这些细胞的策略。该审查旨在通过专注于已知调节的代谢途径和由包括氨基酸,脂质和脂质的MTOR信号传导调节的代谢途径来讨论病原体靶向DC和巨噬细胞代谢的最新洞察力,以讨论如何归因于对其对抗它们的潜在有害免疫反应。碳水化合物新陈代谢和自噬。

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