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代谢性炎症中的脂质信号传导与脂毒性:代谢性疾病发病机制及治疗的指征

Lipid signaling and lipotoxicity in metaflammation: indications for metabolic disease pathogenesis and treatment.

作者信息

Ertunc Meric Erikci, Hotamisligil Gökhan S

机构信息

Department of Genetics and Complex Diseases and Sabri Ülker Center, Harvard T. H. Chan School of Public Health, Broad Institute of Harvard and Massachusetts Institute of Technology, Boston, MA 02115.

Department of Genetics and Complex Diseases and Sabri Ülker Center, Harvard T. H. Chan School of Public Health, Broad Institute of Harvard and Massachusetts Institute of Technology, Boston, MA 02115.

出版信息

J Lipid Res. 2016 Dec;57(12):2099-2114. doi: 10.1194/jlr.R066514. Epub 2016 Jun 21.

Abstract

Lipids encompass a wide variety of molecules such as fatty acids, sterols, phospholipids, and triglycerides. These molecules represent a highly efficient energy resource and can act as structural elements of membranes or as signaling molecules that regulate metabolic homeostasis through many mechanisms. Cells possess an integrated set of response systems to adapt to stresses such as those imposed by nutrient fluctuations during feeding-fasting cycles. While lipids are pivotal for these homeostatic processes, they can also contribute to detrimental metabolic outcomes. When metabolic stress becomes chronic and adaptive mechanisms are overwhelmed, as occurs during prolonged nutrient excess or obesity, lipid influx can exceed the adipose tissue storage capacity and result in accumulation of harmful lipid species at ectopic sites such as liver and muscle. As lipid metabolism and immune responses are highly integrated, accumulation of harmful lipids or generation of signaling intermediates can interfere with immune regulation in multiple tissues, causing a vicious cycle of immune-metabolic dysregulation. In this review, we summarize the role of lipotoxicity in metaflammation at the molecular and tissue level, describe the significance of anti-inflammatory lipids in metabolic homeostasis, and discuss the potential of therapeutic approaches targeting pathways at the intersection of lipid metabolism and immune function.

摘要

脂质包括多种分子,如脂肪酸、固醇、磷脂和甘油三酯。这些分子代表了一种高效的能量来源,可作为膜的结构成分,或作为通过多种机制调节代谢稳态的信号分子。细胞拥有一套完整的反应系统,以适应诸如进食-禁食周期中营养波动所带来的压力。虽然脂质对于这些稳态过程至关重要,但它们也可能导致有害的代谢结果。当代谢应激变得慢性且适应机制不堪重负时,如在长期营养过剩或肥胖期间发生的情况,脂质流入可能超过脂肪组织的储存能力,并导致有害脂质在肝脏和肌肉等异位部位积累。由于脂质代谢和免疫反应高度整合,有害脂质的积累或信号中间体的产生会干扰多个组织中的免疫调节,导致免疫-代谢失调的恶性循环。在这篇综述中,我们总结了脂毒性在分子和组织水平的代谢炎症中的作用,描述了抗炎脂质在代谢稳态中的重要性,并讨论了针对脂质代谢和免疫功能交叉途径的治疗方法的潜力。

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