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戊糖磷酸途径缺陷可降低高脂血症时炎症性巨噬细胞的反应。

A Defective Pentose Phosphate Pathway Reduces Inflammatory Macrophage Responses during Hypercholesterolemia.

机构信息

Amsterdam UMC, University of Amsterdam, Department of Medical Biochemistry, Experimental Vascular Biology, Amsterdam Cardiovascular Sciences, Meibergdreef 9, 1105 AZ Amsterdam, the Netherlands.

Amsterdam UMC, Vrije Universiteit Amsterdam, Department of Molecular Cell Biology and Immunology, Amsterdam Cardiovascular Sciences, Cancer Center Amsterdam, De Boelelaan 1117, 1081 HZ Amsterdam, the Netherlands.

出版信息

Cell Rep. 2018 Nov 20;25(8):2044-2052.e5. doi: 10.1016/j.celrep.2018.10.092.

Abstract

Metabolic reprogramming has emerged as a crucial regulator of immune cell activation, but how systemic metabolism influences immune cell metabolism and function remains to be investigated. To investigate the effect of dyslipidemia on immune cell metabolism, we performed in-depth transcriptional, metabolic, and functional characterization of macrophages isolated from hypercholesterolemic mice. Systemic metabolic changes in such mice alter cellular macrophage metabolism and attenuate inflammatory macrophage responses. In addition to diminished maximal mitochondrial respiration, hypercholesterolemia reduces the LPS-mediated induction of the pentose phosphate pathway (PPP) and the Nrf2-mediated oxidative stress response. Our observation that suppression of the PPP diminishes LPS-induced cytokine secretion supports the notion that this pathway contributes to inflammatory macrophage responses. Overall, this study reveals that systemic and cellular metabolism are strongly interconnected, together dictating macrophage phenotype and function.

摘要

代谢重编程已成为免疫细胞激活的关键调节因子,但系统代谢如何影响免疫细胞代谢和功能仍有待研究。为了研究血脂异常对免疫细胞代谢的影响,我们对来自高胆固醇血症小鼠的巨噬细胞进行了深入的转录组、代谢和功能表征。这些小鼠的系统性代谢变化改变了细胞内巨噬细胞的代谢,并减弱了炎症性巨噬细胞的反应。除了最大线粒体呼吸作用减弱外,高胆固醇血症还降低了 LPS 介导的磷酸戊糖途径 (PPP) 的诱导和 Nrf2 介导的氧化应激反应。我们观察到 PPP 的抑制减少了 LPS 诱导的细胞因子分泌,这支持了该途径有助于炎症性巨噬细胞反应的观点。总的来说,这项研究表明,系统和细胞代谢是紧密相连的,共同决定了巨噬细胞的表型和功能。

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