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白细胞介素1刺激J774单核细胞-巨噬细胞中的胆固醇酯化和胆固醇沉积。

Interleukin 1 stimulates cholesterol esterification and cholesterol deposition in J774 monocytes-macrophages.

作者信息

Mazière C, Barbu V, Auclair M, Mazière J C

机构信息

Département de Biochimie, Faculté de Médecine Saint-Antoine, Paris, France.

出版信息

Biochim Biophys Acta. 1996 Mar 29;1300(1):30-4. doi: 10.1016/0005-2760(95)00232-4.

Abstract

The effects of interleukin 1beta (IL1) in the range of concentration of 10-30 ng/ml on cholesterol metabolism were investigated in the monocyte-macrophage cell line J774. IL1 enhanced cholesterol esterification by [14C]oleic acid and acyl-coenzyme A cholesterol acyl transferase activity in a dose-dependent manner. Incubation of IL1-treated cells with acetylated low density lipoproteins labelled with [3H]cholesteryllinoleate resulted in accumulation of radioactive cholesterol in free and esterified form. Concomitantly, IL1 increased the free and esterified cholesterol intracellular content measured by the cholesterol oxidase technique. The effect of IL1 on cholesterol esterification by oleic acid was not observed in the presence of cycloheximide or of the ACAT inhibitor Sandoz 58 035. IL1 also stimulated cholesterol esterification in other cell types such as human fibroblasts and murine endothelial and smooth muscle cells. The effect of IL1 is specific, since IL2 or tumor necrosis factor (TNF) exhibited no significant activity, whereas oncostatin M only slightly enhanced cholesterol esterification. Since cholesterol deposition is involved in the initiation and progression of the atherosclerotic lesions, these findings highlight the role of the inflammatory cytokine IL1 on this process.

摘要

在单核巨噬细胞系J774中研究了浓度范围为10 - 30 ng/ml的白细胞介素1β(IL1)对胆固醇代谢的影响。IL1以剂量依赖方式增强了[14C]油酸介导的胆固醇酯化作用以及酰基辅酶A胆固醇酰基转移酶活性。用[3H]胆固醇亚油酸酯标记的乙酰化低密度脂蛋白孵育经IL1处理的细胞,导致放射性胆固醇以游离和酯化形式积累。同时,IL1增加了通过胆固醇氧化酶技术测定的细胞内游离胆固醇和酯化胆固醇含量。在存在放线菌酮或ACAT抑制剂山德士58 035的情况下,未观察到IL1对油酸介导的胆固醇酯化的影响。IL1还刺激了其他细胞类型(如人成纤维细胞、小鼠内皮细胞和平滑肌细胞)中的胆固醇酯化。IL1的作用具有特异性,因为IL2或肿瘤坏死因子(TNF)没有显著活性,而抑瘤素M仅略微增强了胆固醇酯化。由于胆固醇沉积参与动脉粥样硬化病变的发生和发展,这些发现突出了炎症细胞因子IL1在此过程中的作用。

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