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体外泡沫细胞形成过程中鼠巨噬细胞中脂蛋白脂肪酶分泌的调节。富含甘油三酯脂蛋白的作用。

Regulation of lipoprotein lipase secretion in murine macrophages during foam cell formation in vitro. Effect of triglyceride-rich lipoproteins.

作者信息

Sofer O, Fainaru M, Schafer Z, Goldman R

机构信息

Department of Medicine A, Beilinson Medical Center, Petah Tikva, Israel.

出版信息

Arterioscler Thromb. 1992 Dec;12(12):1458-66. doi: 10.1161/01.atv.12.12.1458.

Abstract

Triglyceride rich-lipoproteins induce triglyceride accumulation in macrophages, leading to foam cell formation. The correlation between cell triglyceride accumulation and lipoprotein lipase (LPL) secretion in murine macrophages and the role that LPL plays in the accumulation process were examined. LPL secretion is defined as the extracellular LPL activity that accumulates during a 4-hour incubation of treated and untreated cells in a bovine serum albumin-containing RPMI-1640 medium. LPL secretion was suppressed (up to 70%) in a dose- and time-dependent manner when J774.1 cells were incubated with chylomicrons, very low density lipoproteins, and intermediate density lipoproteins but not with low or high density lipoproteins from normolipidemic and hypertriglyceridemic subjects. Oleic acid both suppressed LPL secretion and invoked triglyceride accumulation. Suppression of LPL secretion preceded gross triglyceride accumulation, was reversible, and was not the result of a reduction in LPL mRNA. P388D1 cells neither secreted LPL nor accumulated triglyceride. Inhibition of LPL secretion by tunicamycin in both peritoneal macrophages and J774.1 cells prevented a hypertriglyceridemic very low density lipoprotein-induced triglyceride accumulation, an effect that was counteracted by addition of exogenous LPL. The results suggest that 1) extracellular hydrolysis of lipoprotein triglyceride is a major factor in inducing foam cell formation and 2) LPL secretion may be regulated by cell energy needs, and when these needs are exceeded, LPL secretion is suppressed.

摘要

富含甘油三酯的脂蛋白会诱导巨噬细胞内甘油三酯积聚,导致泡沫细胞形成。研究了小鼠巨噬细胞中细胞甘油三酯积聚与脂蛋白脂肪酶(LPL)分泌之间的相关性以及LPL在积聚过程中所起的作用。LPL分泌定义为在含牛血清白蛋白的RPMI-1640培养基中处理和未处理的细胞孵育4小时期间积累的细胞外LPL活性。当J774.1细胞与乳糜微粒、极低密度脂蛋白和中间密度脂蛋白孵育时,LPL分泌以剂量和时间依赖性方式受到抑制(高达70%),但与来自正常血脂和高甘油三酯血症受试者的低密度或高密度脂蛋白孵育时则不受抑制。油酸既抑制LPL分泌又引发甘油三酯积聚。LPL分泌的抑制先于总甘油三酯积聚,是可逆的,且不是LPL mRNA减少的结果。P388D1细胞既不分泌LPL也不积聚甘油三酯。衣霉素对腹膜巨噬细胞和J774.1细胞中LPL分泌的抑制可防止高甘油三酯血症极低密度脂蛋白诱导的甘油三酯积聚,添加外源性LPL可抵消这一作用。结果表明:1)脂蛋白甘油三酯的细胞外水解是诱导泡沫细胞形成的主要因素;2)LPL分泌可能受细胞能量需求调节,当这些需求超过限度时,LPL分泌会受到抑制。

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