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血管紧张素II通过诱导I型B类清道夫受体,促进牛肾上腺球状带细胞和人肾上腺皮质癌细胞对高密度脂蛋白胆固醇酯的选择性摄取。

Angiotensin II promotes selective uptake of high density lipoprotein cholesterol esters in bovine adrenal glomerulosa and human adrenocortical carcinoma cells through induction of scavenger receptor class B type I.

作者信息

Cherradi N, Bideau M, Arnaudeau S, Demaurex N, James R W, Azhar S, Capponi A M

机构信息

Division of Endocrinology and Diabetology, Faculty of Medicine, University Hospital, CH-1211 Geneva, Switzerland.

出版信息

Endocrinology. 2001 Oct;142(10):4540-9. doi: 10.1210/endo.142.10.8412.

DOI:10.1210/endo.142.10.8412
PMID:11564720
Abstract

Angiotensin II is one of the main physiological regulators of aldosterone biosynthesis in the zona glomerulosa of the adrenal cortex. The hormone stimulates intracellular cholesterol mobilization to the mitochondrion for steroid biosynthesis. Here we have examined whether angiotensin II also modulates exogenous lipoprotein cholesterol ester supply to the steroidogenic machinery and whether this control is exerted on the selective transport of high density lipoprotein-derived cholesterol ester to intracellular lipid droplets through the scavenger receptor class B type I. In bovine adrenal glomerulosa and human NCI H295R adrenocortical carcinoma cells, high density lipoprotein stimulated steroid production. Angiotensin II pretreatment for 24 h potentiated this response. Fluorescence microscopy of cellular uptake of reconstituted high density lipoprotein containing a fluorescent cholesterol ester revealed an initial, time-dependent narrow labeling of the cell membrane followed by an intense accumulation of the fluorescent cholesterol ester within lipid droplets. At all time points, labeling was more pronounced in cells that had been treated for 24 h with angiotensin II. Fluorescence incorporation into cells was prevented by a monoclonal antibody directed against apolipoprotein A-I. Upon quantitative fluorometric determination, cholesterol ester uptake in angiotensin II-treated bovine cells was increased to 175 +/- 15% of controls after 2 h and to 260 +/- 10% after 4 h of exposure to fluorescent high density lipoprotein. The amount of scavenger receptor class B type I protein detected in cells treated with angiotensin II for 24 h reached 203 +/- 12% of that measured in control cells (n = 3, P < 0.01). In contrast, low density lipoprotein receptors were only minimally affected by angiotensin II treatment. This increase in scavenger receptor class B type I protein was associated with a 3-fold induction of scavenger receptor class B type I mRNA, which could be prevented by actinomycin D but not by cycloheximide. Similar results were obtained in the human adenocarcinoma cell line H295R. These observations show that angiotensin II regulates the scavenger receptor class B type I-mediated selective transport of lipoprotein cholesterol ester across the cell membrane as a major source of precursor for mineralocorticoid biosynthesis in both human and bovine adrenal cells.

摘要

血管紧张素II是肾上腺皮质球状带醛固酮生物合成的主要生理调节因子之一。该激素刺激细胞内胆固醇向线粒体转运以进行类固醇生物合成。在此,我们研究了血管紧张素II是否也调节外源性脂蛋白胆固醇酯向类固醇生成机制的供应,以及这种调控是否通过I型B类清道夫受体作用于高密度脂蛋白衍生的胆固醇酯向细胞内脂滴的选择性转运。在牛肾上腺球状带细胞和人NCI H295R肾上腺皮质癌细胞中,高密度脂蛋白刺激类固醇生成。血管紧张素II预处理24小时可增强这种反应。对含有荧光胆固醇酯的重组高密度脂蛋白进行细胞摄取的荧光显微镜观察显示,最初细胞膜出现时间依赖性的窄标记,随后荧光胆固醇酯在脂滴内大量积聚。在所有时间点,用血管紧张素II处理24小时的细胞中的标记更为明显。针对载脂蛋白A-I的单克隆抗体可阻止荧光掺入细胞。经荧光定量测定,在暴露于荧光高密度脂蛋白2小时后,血管紧张素II处理的牛细胞中胆固醇酯摄取增加至对照的175±15%,4小时后增加至260±10%。在用血管紧张素II处理24小时的细胞中检测到的I型B类清道夫受体蛋白量达到对照细胞中测量值的203±12%(n = 3,P < 0.01)。相比之下,低密度脂蛋白受体仅受到血管紧张素II处理的轻微影响。I型B类清道夫受体蛋白的这种增加与I型B类清道夫受体mRNA的3倍诱导相关,放线菌素D可阻止这种诱导,但环己酰亚胺不能。在人腺癌细胞系H295R中也获得了类似结果。这些观察结果表明,血管紧张素II调节I型B类清道夫受体介导的脂蛋白胆固醇酯跨细胞膜的选择性转运,这是人和牛肾上腺细胞中盐皮质激素生物合成前体的主要来源。

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