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ATP结合盒转运蛋白A7(ABCA7)与载脂蛋白A-I结合,并介导细胞磷脂而非胆固醇流出。

ATP-binding cassette transporter A7 (ABCA7) binds apolipoprotein A-I and mediates cellular phospholipid but not cholesterol efflux.

作者信息

Wang Nan, Lan Debin, Gerbod-Giannone Marie, Linsel-Nitschke Patrick, Jehle Andreas Werner, Chen Wengen, Martinez Laurent O, Tall Alan R

机构信息

Division of Molecular Medicine, Department of Medicine, Columbia University, New York, New York 10032, USA.

出版信息

J Biol Chem. 2003 Oct 31;278(44):42906-12. doi: 10.1074/jbc.M307831200. Epub 2003 Aug 12.

Abstract

ATP-binding cassette transporter 1 (ABCA1), the defective transporter in Tangier disease, binds and promotes cellular cholesterol and phospholipid efflux to apolipoprotein I (apoA-I). Based on a high degree of sequence homology between ABCA1 and ABCA7, a transporter of unknown function, we investigated the possibility that ABCA7 might be involved in apolipoprotein binding and lipid efflux. Similarly to cells expressing ABCA1, HEK293 cells overexpressing ABCA7 showed specific binding and cross-linking of lipid-poor apoA-I. ABCA7 expression increased cellular phosphatidylcholine and sphingomyelin efflux to apoA-I in a manner similar to ABCA1 but had no effect on cholesterol efflux. Western analysis showed a high protein level of ABCA7 in mouse spleen, lung, adrenal, and brain but low expression in liver. In contrast to ABCA1, ABCA7 showed moderate basal mRNA and protein levels in macrophages and lymphocytes but no induction by liver X receptor activation. These studies show that ABCA7 has the ability to bind apolipoproteins and promote efflux of cellular phospholipids without cholesterol, and they suggest a possible role of ABCA7 in cellular phospholipid metabolism in peripheral tissues.

摘要

三磷酸腺苷结合盒转运蛋白1(ABCA1)是丹吉尔病中的缺陷转运蛋白,它能结合并促进细胞内胆固醇和磷脂向载脂蛋白I(apoA-I)的流出。基于ABCA1与功能未知的转运蛋白ABCA7之间高度的序列同源性,我们研究了ABCA7可能参与载脂蛋白结合和脂质流出的可能性。与表达ABCA1的细胞类似,过表达ABCA7的HEK293细胞显示出脱脂apoA-I的特异性结合和交联。ABCA7的表达以类似于ABCA1的方式增加了细胞磷脂酰胆碱和鞘磷脂向apoA-I的流出,但对胆固醇流出没有影响。蛋白质印迹分析显示,ABCA7在小鼠脾脏、肺、肾上腺和脑中的蛋白质水平较高,但在肝脏中的表达较低。与ABCA1不同,ABCA7在巨噬细胞和淋巴细胞中显示出中等水平的基础mRNA和蛋白质水平,但不会因肝X受体激活而诱导表达。这些研究表明,ABCA7具有结合载脂蛋白并促进细胞磷脂(而非胆固醇)流出的能力,并且提示ABCA7在外周组织的细胞磷脂代谢中可能发挥作用。

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