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乳糜微粒残粒诱导巨噬细胞泡沫细胞形成。

The induction of macrophage foam cell formation by chylomicron remnants.

作者信息

Botham K M, Moore E H, De Pascale C, Bejta F

机构信息

Department of Veterinary Basic Sciences, The Royal Veterinary College, Royal College Street, London NW1 0TU, UK.

出版信息

Biochem Soc Trans. 2007 Jun;35(Pt 3):454-8. doi: 10.1042/BST0350454.

Abstract

The accumulation of foam cells in the artery wall causes fatty streaks, the first lesions in atherosclerosis. LDL (low-density lipoprotein) plays a major role in foam cell formation, although prior oxidation of the particles is required. Recent studies, however, have provided considerable evidence to indicate that CMRs (chylomicron remnants), which carry dietary lipids in the blood, induce foam cell formation without oxidation. We have shown that CMRs are taken up by macrophages and induce accumulation of both triacylglycerol and cholesterol, and that the rate of uptake and amount of lipid accumulated is influenced by the type of dietary fat in the particles. Furthermore, oxidation of CMRs, in striking contrast with LDL, inhibits, rather than enhances, their uptake and induction of lipid accumulation. In addition, the lipid accumulated after exposure of macrophages to CMRs is resistant to efflux, and this may be due to its sequestration in lysosomes. These findings demonstrate that CMRs induce pro-atherogenic changes in macrophages, and that their effects may be modulated by dietary factors including oxidized fats, lipophilic antioxidants and the type of fat present.

摘要

动脉壁中泡沫细胞的积累会导致脂肪条纹,这是动脉粥样硬化的首个病变。低密度脂蛋白(LDL)在泡沫细胞形成中起主要作用,不过这些颗粒需要事先氧化。然而,最近的研究提供了大量证据表明,在血液中携带膳食脂质的乳糜微粒残余物(CMRs)可在不发生氧化的情况下诱导泡沫细胞形成。我们已经表明,CMRs被巨噬细胞摄取,并诱导三酰甘油和胆固醇的积累,并且摄取速率和积累的脂质量受颗粒中膳食脂肪类型的影响。此外,与LDL形成鲜明对比的是,CMRs的氧化会抑制而非增强它们的摄取和脂质积累诱导作用。另外,巨噬细胞暴露于CMRs后积累的脂质难以流出,这可能是由于其被隔离在溶酶体中。这些发现表明,CMRs会在巨噬细胞中诱导促动脉粥样硬化变化,并且它们的作用可能会受到包括氧化脂肪、亲脂性抗氧化剂和存在的脂肪类型等膳食因素的调节。

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