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I型清道夫受体B类作为细胞胆固醇向脂蛋白和磷脂受体流出的介质。

Scavenger receptor class B type I as a mediator of cellular cholesterol efflux to lipoproteins and phospholipid acceptors.

作者信息

Jian B, de la Llera-Moya M, Ji Y, Wang N, Phillips M C, Swaney J B, Tall A R, Rothblat G H

机构信息

Department of Biochemistry, Allegheny University of the Health Sciences, Philadelphia, Pennsylvania 19129, USA.

出版信息

J Biol Chem. 1998 Mar 6;273(10):5599-606. doi: 10.1074/jbc.273.10.5599.

Abstract

We recently reported that the rate of efflux of cholesterol from cells to high density lipoprotein (HDL) was related to the expression level of scavenger receptor class B type I (SR-BI). Moreover, the expression of this receptor in atheromatous arteries raises the possibility that SR-BI mediates cholesterol efflux in the arterial wall (Ji, Y., Jian, B., Wang, N., Sun, Y., de la Llera Moya, M., Phillips, M. C., Rothblat, G. H., Swaney, J. B., and Tall, A. R. (1997) J. Biol. Chem. 272, 20982-20985). In this paper we describe studies that suggest that the presence of phospholipid on acceptor particles plays an important role in modulating interaction with the SR-BI. Specifically, enrichment of serum with phospholipid resulted in marked stimulation of cholesterol efflux from cells that had higher levels of SR-BI expression, like Fu5AH or Y1-BS1 cells, and little or no stimulation in cells with low SR-BI levels, such as Y-1 cells. Stimulation of efflux by phospholipid enrichment was also a function of SR-BI levels in Chinese hamster ovary cells transfected with the SR-BI gene. Efflux to protein-free vesicles prepared with 1-palmitoyl-2-oleoylphosphatidyl-choline also correlated with SR-BI levels, suggesting that phospholipid, as well as protein, influences the interaction that results in cholesterol efflux. By contrast, cholesterol efflux from a non-cell donor showed no stimulation consequent to phospholipid enrichment of the serum acceptor. These results may help to explain observations in the literature that document an increased risk of atherosclerosis in patients with depressed levels of HDL phospholipid even in the face of normal HDL cholesterol levels.

摘要

我们最近报道,细胞内胆固醇向高密度脂蛋白(HDL)的流出速率与I型清道夫受体(SR-BI)的表达水平相关。此外,该受体在动脉粥样硬化动脉中的表达增加了SR-BI介导动脉壁胆固醇流出的可能性(Ji, Y., Jian, B., Wang, N., Sun, Y., de la Llera Moya, M., Phillips, M. C., Rothblat, G. H., Swaney, J. B., and Tall, A. R. (1997) J. Biol. Chem. 272, 20982-20985)。在本文中,我们描述的研究表明,受体颗粒上磷脂的存在在调节与SR-BI的相互作用中起重要作用。具体而言,用磷脂富集血清可显著刺激SR-BI表达水平较高的细胞(如Fu5AH或Y1-BS1细胞)的胆固醇流出,而对SR-BI水平较低的细胞(如Y-1细胞)几乎没有刺激作用。用SR-BI基因转染的中国仓鼠卵巢细胞中,磷脂富集对流出的刺激作用也与SR-BI水平有关。向用1-棕榈酰-2-油酰磷脂酰胆碱制备的无蛋白囊泡的流出也与SR-BI水平相关,这表明磷脂以及蛋白质都会影响导致胆固醇流出的相互作用。相比之下,来自非细胞供体的胆固醇流出在血清受体用磷脂富集后没有受到刺激。这些结果可能有助于解释文献中的观察结果,即即使HDL胆固醇水平正常,HDL磷脂水平降低的患者患动脉粥样硬化的风险也会增加。

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