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在缺乏清道夫受体A的THP-1细胞系中氧化低密度脂蛋白的摄取。

Uptake of oxidized low-density lipoprotein in a THP-1 cell line lacking scavenger receptor A.

作者信息

Sugano R, Yamamura T, Harada-Shiba M, Miyake Y, Yamamoto A

机构信息

Department of Etiology and Pathophysiology, National Cardiovascular Center Research Institute, 5-7-1 Fujishiro-dai, Suita, Osaka 565-8565, Japan.

出版信息

Atherosclerosis. 2001 Oct;158(2):351-7. doi: 10.1016/s0021-9150(01)00456-7.

Abstract

We previously isolated THP-1 subtype cells (sTHP-1), a cell line that expresses scanty amounts of scavenger receptor A (ScR-A) and does not undergo foam cell formation when incubated with acetylated low-density lipoprotein (Ac-LDL). In this study, we investigated the accumulation of esterified cholesterol in sTHP-1 cells incubated with oxidized LDL (Ox-LDL), a physiologically modified lipoprotein in human. While sTHP-1 cells incubated with Ac-LDL accumulated only small amounts of esterified cholesterol, those incubated with Ox-LDL accumulated amounts similar to those accumulated by parent THP-1 (pTHP-1) cells. sTHP-1 cells expressed CD36 in amounts similar to the amounts expressed by pTHP-1 cells, and Ox-LDL was internalized through this CD36. The amount of accumulated esterified cholesterol was 73-81% of that accumulated in pTHP-1 cells expressing ScR-A. The levels of 125I-Ox-LDL binding, association, and degradation in sTHP-1 cells were 64-70% of the corresponding levels in pTHP-1 cells. In our experiments utilizing ScR-A-deficient sTHP-1 cells and a specific antibody against human CD36, most of the Ox-LDL interacted with the CD36 receptor. In addition, a substantial amount of Ox-LDL (28-42%) was bound and degraded by sTHP-1 macrophages when both of the two major scavenger receptors, ScR-A and CD36, were deficient or blocked. These results indicate that CD36 in macrophages plays an important role in foam cell formation by Ox-LDL, while additional scavenger receptor(s) may take part in significant pathways of Ox-LDL uptake in macrophages.

摘要

我们之前分离出了THP-1亚型细胞(sTHP-1),该细胞系表达少量的清道夫受体A(ScR-A),并且在与乙酰化低密度脂蛋白(Ac-LDL)孵育时不会形成泡沫细胞。在本研究中,我们调查了用氧化低密度脂蛋白(Ox-LDL,一种人体内生理修饰的脂蛋白)孵育的sTHP-1细胞中酯化胆固醇的积累情况。当sTHP-1细胞与Ac-LDL孵育时,仅积累少量的酯化胆固醇,而与Ox-LDL孵育的细胞积累的量与亲本THP-1(pTHP-1)细胞积累的量相似。sTHP-1细胞表达的CD36量与pTHP-1细胞表达的量相似,并且Ox-LDL通过这种CD36被内化。积累的酯化胆固醇量是表达ScR-A的pTHP-1细胞中积累量的73 - 81%。sTHP-1细胞中125I-Ox-LDL的结合、缔合和降解水平是pTHP-1细胞中相应水平的64 - 70%。在我们利用缺乏ScR-A的sTHP-1细胞和抗人CD36特异性抗体的实验中,大多数Ox-LDL与CD36受体相互作用。此外,当两种主要的清道夫受体ScR-A和CD36都缺乏或被阻断时,大量的Ox-LDL(28 - 42%)被sTHP-1巨噬细胞结合并降解。这些结果表明,巨噬细胞中的CD36在Ox-LDL诱导的泡沫细胞形成中起重要作用,而其他清道夫受体可能参与巨噬细胞摄取Ox-LDL的重要途径。

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