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小窝蛋白-1(Cav-1)对血管平滑肌(VSM)细胞中脂肪酸摄取、CD36定位及脂毒性的影响。

The effect of caveolin-1 (Cav-1) on fatty acid uptake and CD36 localization and lipotoxicity in vascular smooth muscle (VSM) cells.

作者信息

Mattern Heather M, Raikar Leena S, Hardin Christopher D

机构信息

Department of Medical Pharmacology and Physiology, University of Missouri Columbia, MO 65212, USA.

出版信息

Int J Physiol Pathophysiol Pharmacol. 2009;1(1):1-14. Epub 2008 Nov 20.

Abstract

The purpose of this study was to determine whether caveolin-1 (Cav-1) is involved in lipotoxicity in vascular smooth muscle (VSM) cells by altering CD36 membrane localization. Normal A7r5 cells (cultured rat aortic smooth muscle cells), Cav-1 overexpressing cells, and cells treated with 10 mM cyclodextrin for 30 minutes were immunolabeled with Cav-1 and CD36. The peripheral to central ratio of CD36 in Cav-1 overexpressing cells (1.52±0.19) was significantly higher than in control cells (1.05±0.16, p=0.035) and cyclodextrin-treated cells (0.861±0.279, p=0.035). Fatty acid uptake at 5, 10, and 15 seconds was quantified with fluorescence of C1BODIPY 500/510 C12, a long-chain fatty acid analog. A7r5 VSM cells overexpressing Cav-1 had decrease a in the rate of fatty acid uptake compared to control cells. Cells treated with cyclodextrin also had a decrease in fatty acid uptake compared to control. Cav-1 overexpressing cells incubated in 0.05 mM palmitate had 31.4±8.8% apoptosis, where only 3.9±1.0% of Cav-1 overexpressing cells incubated in palmitate were apoptotic (p=0.044). Cyclodextrin treatment resulted in a decrease in apoptosis in cells incubated in 0.1 mM palmitate (69.7±2.1%) compared to control cells incubated in palmitate (85.6±2.7%) (p=0.003). These data suggest that in cells overexpressing Cav-1, CD36 is relocated to the plasma membrane of VSM cells, where it may play an increased role in fatty acid uptake and possibly lipotoxicity.

摘要

本研究的目的是确定小窝蛋白-1(Cav-1)是否通过改变CD36的膜定位参与血管平滑肌(VSM)细胞的脂毒性。用Cav-1和CD36对正常A7r5细胞(培养的大鼠主动脉平滑肌细胞)、Cav-1过表达细胞以及用10 mM环糊精处理30分钟的细胞进行免疫标记。Cav-1过表达细胞中CD36的外周与中央比率(1.52±0.19)显著高于对照细胞(1.05±0.16,p = 0.035)和环糊精处理细胞(0.861±0.279,p = 0.035)。用长链脂肪酸类似物C1BODIPY 500/510 C12的荧光对5、10和15秒时的脂肪酸摄取进行定量。与对照细胞相比,过表达Cav-1的A7r5 VSM细胞的脂肪酸摄取速率降低。与对照相比,用环糊精处理的细胞的脂肪酸摄取也减少。在0.05 mM棕榈酸中孵育的Cav-1过表达细胞有31.4±8.8%的细胞凋亡,而在棕榈酸中孵育的Cav-1过表达细胞仅有3.9±1.0%凋亡(p = 0.044)。与在棕榈酸中孵育的对照细胞(85.6±2.7%)相比,环糊精处理导致在0.1 mM棕榈酸中孵育的细胞凋亡减少(69.7±2.1%)(p = 0.003)。这些数据表明,在过表达Cav-1的细胞中,CD36重新定位于VSM细胞的质膜,在那里它可能在脂肪酸摄取以及可能的脂毒性中发挥更大作用。

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