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缺氧与内质网应激反应的串扰:巨噬细胞极化的关键调节因子。

Crosstalk Between Hypoxia and ER Stress Response: A Key Regulator of Macrophage Polarization.

机构信息

Translational Immunology Laboratory, Health Research Institute of the Principality of Asturias, Hospital Universitario Central de Asturias, Oviedo, Spain.

Immunology Service, Hospital Universitario Central de Asturias, Oviedo, Spain.

出版信息

Front Immunol. 2020 Jan 8;10:2951. doi: 10.3389/fimmu.2019.02951. eCollection 2019.

Abstract

Macrophage activation and polarization are closely linked with metabolic rewiring, which is required to sustain their biological functions. These metabolic alterations allow the macrophages to adapt to the microenvironment changes associated with inflammation or tissue damage (hypoxia, nutrient imbalance, oxidative stress, etc.) and to fulfill their highly energy-demanding proinflammatory and anti-microbial functions. This response is integrated via metabolic sensors that coordinate these metabolic fluxes with their functional requirements. Here we review how the metabolic and phenotypic plasticity of macrophages are intrinsically connected with the hypoxia stress sensors and the unfolded protein response in the endoplasmic reticulum, and how these molecular pathways participate in the maladaptive polarization of macrophages in human pathology and chronic inflammation.

摘要

巨噬细胞的激活和极化与代谢重编程密切相关,这是维持其生物学功能所必需的。这些代谢改变使巨噬细胞能够适应与炎症或组织损伤相关的微环境变化(缺氧、营养失衡、氧化应激等),并完成其高能量需求的促炎和抗微生物功能。这种反应是通过代谢传感器来整合的,这些传感器将这些代谢通量与它们的功能需求协调起来。在这里,我们回顾了巨噬细胞的代谢和表型可塑性如何与缺氧应激传感器和内质网中的未折叠蛋白反应内在联系起来,以及这些分子途径如何参与人类病理学和慢性炎症中巨噬细胞的适应性极化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/74ab/6961549/2cb9e6f6ac7a/fimmu-10-02951-g0001.jpg

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