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磷脂消耗对重组高密度脂蛋白的大小、结构和重塑的影响。

Influence of phospholipid depletion on the size, structure, and remodeling of reconstituted high density lipoproteins.

作者信息

Rye K A, Duong M N

机构信息

Lipid Research Laboratory, Hanson Centre for Cancer Research, Adelaide, South Australia, Australia 5000.

出版信息

J Lipid Res. 2000 Oct;41(10):1640-50.

Abstract

This study shows that phospholipid depletion has a major impact on the size and structure of spherical, reconstituted high density lipoproteins (rHDL) and their remodeling by cholesteryl ester transfer protein (CETP). Spherical rHDL, 9.2 nm in diameter with a phospholipid/cholesteryl ester/unesterified cholesterol/apolipoprotein A-I (apoA-I) (PL/CE/UC/A-I) molar ratio of 37.3/24.5/4.1/1.0, were depleted progressively of phospholipids by incubation with phospholipase A(2). After 30 min of incubation the PL/CE/UC/A-I molar ratio of the rHDL was 8.0/31.2/4.4/1.0 and their diameter had decreased to 8.0 nm. Comparable changes in rHDL size and composition were also apparent when the incubations were carried out in the presence of other lipoprotein classes and lipoprotein-deficient plasma. The changes in size and composition were not accompanied by the dissociation of apoA-I from the rHDL. Phospholipid depletion did not affect rHDL surface charge or the structure and stability of apoA-I. The remodeling of unmodified and phospholipid-depleted rHDL by CETP was also investigated. When the rHDL were incubated for 3 h with CETP and Intralipid, transfers of core lipids between the phospholipid-depleted rHDL and Intralipid were decreased relative to unmodified rHDL. This difference was no longer apparent when the incubations were extended beyond 3 h. In these incubations apoA-I dissociated from the phospholipid-depleted and unmodified rHDL at 3 and 12 h, respectively. At 24 h the respective diameters of the unmodified rHDL and phospholipid-depleted rHDL were 8.0 and 7.8 nm. In conclusion, phospholipid depletion has a major impact on rHDL size and their remodeling by CETP.

摘要

本研究表明,磷脂耗竭对球形重组高密度脂蛋白(rHDL)的大小和结构及其被胆固醇酯转运蛋白(CETP)重塑有重大影响。直径为9.2 nm的球形rHDL,其磷脂/胆固醇酯/未酯化胆固醇/载脂蛋白A-I(apoA-I)(PL/CE/UC/A-I)摩尔比为37.3/24.5/4.1/1.0,通过与磷脂酶A(2)孵育逐渐消耗磷脂。孵育30分钟后,rHDL的PL/CE/UC/A-I摩尔比为8.0/31.2/4.4/1.0,其直径降至8.0 nm。当在其他脂蛋白类别和脂蛋白缺乏血浆存在的情况下进行孵育时,rHDL大小和组成的类似变化也很明显。大小和组成的变化并未伴随apoA-I从rHDL上解离。磷脂耗竭不影响rHDL表面电荷或apoA-I的结构和稳定性。还研究了CETP对未修饰和磷脂耗竭的rHDL的重塑作用。当rHDL与CETP和英脱利匹特孵育3小时时,相对于未修饰的rHDL,磷脂耗竭的rHDL与英脱利匹特之间核心脂质的转移减少。当孵育时间延长至3小时以上时,这种差异不再明显。在这些孵育中,apoA-I分别在3小时和12小时从磷脂耗竭的rHDL和未修饰的rHDL上解离。在24小时时,未修饰的rHDL和磷脂耗竭的rHDL的各自直径分别为8.0和7.8 nm。总之,磷脂耗竭对rHDL大小及其被CETP重塑有重大影响。

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