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缩醛磷脂参与高密度脂蛋白介导的胆固醇流出:来自对缩醛磷脂缺陷细胞研究的见解。

Plasmalogen phospholipids are involved in HDL-mediated cholesterol efflux: insights from investigations with plasmalogen-deficient cells.

作者信息

Mandel H, Sharf R, Berant M, Wanders R J, Vreken P, Aviram M

机构信息

Department of Pediatrics, Rambam Medical Center, Haifa, Israel.

出版信息

Biochem Biophys Res Commun. 1998 Sep 18;250(2):369-73. doi: 10.1006/bbrc.1998.9321.

Abstract

Plasmalogens are ether-glycerophospholipids that exist in all mammalian cells, but their physiological function remains thus far an enigma. It has been previously suggested that the association of high-density lipoprotein (HDL) with cellular phospholipid is a pre-requisite for the process of HDL-mediated cholesterol efflux (HDL-MCE). To investigate our hypothesis that plasmalogens might play a role in HDL-MCE, we used a model composed of plasmalogen-deficient cells including RAW mutant macrophages and fibroblasts from patients with rhizomelic chondrodysplasia punctata type II. In mutant macrophages, HDL-MCE was reduced by 57% compared to control macrophages, after 16 hours. A similar phenomenon was observed in plasmalogen-deficient patients fibroblasts. Incubation of plasmalogen-deficient fibroblasts with 1-0-hexadecyl-sn-glycerol, which restored plasmalogen levels to that of control cells, resulted in a 35% increase in HDL-MCE, compared to a 10% increment in controls. The novel finding that HDL-MCE is reduced in plasmalogen-deficient cells and increases following plasmalogen restoration leads us to suggest that plasmalogen has an important function in the mediation of cellular cholesterol efflux.

摘要

缩醛磷脂是存在于所有哺乳动物细胞中的醚甘油磷脂,但其生理功能至今仍是个谜。此前有研究表明,高密度脂蛋白(HDL)与细胞磷脂的结合是HDL介导的胆固醇流出(HDL-MCE)过程的先决条件。为了验证我们关于缩醛磷脂可能在HDL-MCE中发挥作用的假设,我们使用了一个由缺乏缩醛磷脂的细胞组成的模型,包括RAW突变巨噬细胞和II型肢根型点状软骨发育不良患者的成纤维细胞。在突变巨噬细胞中,16小时后,与对照巨噬细胞相比,HDL-MCE降低了57%。在缺乏缩醛磷脂的患者成纤维细胞中也观察到了类似现象。用1-0-十六烷基-sn-甘油孵育缺乏缩醛磷脂的成纤维细胞,可使缩醛磷脂水平恢复到对照细胞水平,与对照细胞增加10%相比,HDL-MCE增加了35%。在缺乏缩醛磷脂的细胞中HDL-MCE降低,而在缩醛磷脂恢复后增加,这一新发现使我们认为缩醛磷脂在介导细胞胆固醇流出中具有重要作用。

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