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The impact of dietary fatty acids on macrophage cholesterol homeostasis

机译:膳食脂肪酸对巨噬细胞胆固醇稳态的影响

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The impact of dietary fatty acids in atherosclerosis development may be partially attributed to their effect on macrophage cholesterol homeostasis. This process is the result of interplay between cholesterol uptake and efflux, which are permeated by inflammation and oxidative stress. Although saturated fatty acids (SAFAs) do not influence cholesterol efflux, they trigger endoplasmic reticulum stress, which culminates in increased lectin-like oxidized LDL (oxLDL) receptor (LOX1) expression and, consequently, oxLDL uptake, leading to apoptosis. Unsaturated fatty acids prevent most SAFAs-mediated deleterious effects and are generally associated with reduced cholesterol efflux, although alpha-linolenic acid increases cholesterol export. Trans fatty acids increase macrophage cholesterol content by reducing ABCA-1 expression, leading to strong atherosclerotic plaque formation. As isomers of conjugated linoleic acid (CLAs) are strong PPAR gamma ligands, they induce cluster of differentiation (CD36) expression, increasing intracellular cholesterol content. Considering the multiple effects of fatty acids on intracellular signaling pathways, the purpose of this review is to address the role of dietary fat in several mechanisms that control macrophage lipid content, which can determine the fate of atherosclerotic lesions. (C) 2014 Elsevier Inc. All rights reserved.
机译:饮食脂肪酸对动脉粥样硬化发展的影响可能部分归因于它们对巨噬细胞胆固醇稳态的影响。该过程是胆固醇摄取和外排相互作用的结果,胆固醇的摄取和外排被炎症和氧化应激渗透。尽管饱和脂肪酸(SAFA)不会影响胆固醇外排,但它们会触发内质网应激,最终导致凝集素样氧化LDL(oxLDL)受体(LOX1)表达增加,并因此导致oxLDL吸收,从而导致细胞凋亡。不饱和脂肪酸可防止大多数SAFA介导的有害作用,尽管α-亚麻酸会增加胆固醇的输出,但通常会降低胆固醇的流出。反式脂肪酸通过降低ABCA-1表达来增加巨噬细胞胆固醇含量,导致形成强烈的动脉粥样硬化斑块。由于共轭亚油酸(CLA)的异构体是强PPARγ配体,因此它们诱导分化簇(CD36)表达,从而增加了细胞内胆固醇的含量。考虑到脂肪酸对细胞内信号通路的多重影响,本文的目的是探讨饮食脂肪在控制巨噬细胞脂质含量的几种机制中的作用,这些机制可以决定动脉粥样硬化病变的命运。 (C)2014 Elsevier Inc.保留所有权利。

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