首页> 外文期刊>The Biochemical Journal >Regulation of plasma glycero-lysophospholipid levels by lipoprotein metabolism
【24h】

Regulation of plasma glycero-lysophospholipid levels by lipoprotein metabolism

机译:通过脂蛋白代谢调节血浆甘油溶血磷脂水平

获取原文
获取原文并翻译 | 示例
           

摘要

Glycero-lysophospholipids, such as lysophosphatidic acids and lysophosphatidylserine, are gathering attention, since specific receptors have been identified. Most of these compounds have been proposed to be bound to albumin, while their associations with lipoproteins have not been fully elucidated. Therefore, in this study, we aimed to investigate the contents of glycero-lysophospholipids (lysophosphatidic acids, lysophosphatidylcholine, lysophosphatidylethanolamine, lysophosphatidylglycerol, lysophosphatidylinositol, and lysophosphatidylserine) on lipoproteins and the modulation of their metabolism by lipoprotein metabolism. We observed that moderate amounts of glycero-lysophospholipids, with the exception of lysophosphatidylserine, were distributed on the LDL and HDL fractions, and glycero-lysophospholipids that had bound to albumin were observed in lipoprotein fractions when they were co-incubated. The overexpression of cholesteryl ester transfer protein decreased the plasma levels of lysophosphatidylcholine, lysophosphatidylethanolamine, lysophosphatidylglycerol, and lysophosphatidylinositol and it increased their contents in apoB-containing lipoproteins, while it decreased their contents in HDL and lipoprotein-depleted fractions in mice. The overexpression of the LDL receptor (LDLr) decreased the plasma levels of lysophosphatidylcholine, lysophosphatidylethanolamine, lysophosphatidylglycerol, and lysophosphatidylinositol and decreased the contents of these compounds in the LDL, HDL, and lipoprotein-depleted fractions, while the knockdown of the LDLr increased them. These results suggest the potential importance of glycero-lysophospholipids in the pleiotropic effects of lipoproteins as well as the importance of lipoprotein metabolism in the regulation of glycero-lysophospholipids.
机译:由于已经鉴定了特异性受体,甘油 - 溶血磷脂如溶血磷脂酸和溶血磷脂酰丝氨酸,例如溶血磷脂酸和溶血磷脂酰丝氨酸。已经提出了大多数这些化合物以与白蛋白结合,同时它们与脂蛋白的关联未得到完全阐明。因此,在本研究中,我们旨在研究甘油 - 溶血磷脂(溶血磷脂酸,溶血磷脂酰胆碱,溶血磷脂酰乙氨基甲胺,溶血磷脂酰甘油,溶血磷苷素,溶血磷脂酰磷素)和脂蛋白代谢的调节。我们观察到,在LDL和HDL级分外分布在LDL和HDL级分外,中等量的甘油溶血磷脂,并且当它们共孵育时,在脂蛋白级分中观察到与白蛋白结合的甘油 - 溶血磷脂。胆甾醇酯转移蛋白的过表达降低了溶血磷脂酰胆碱,溶血磷脂酰乙醇胺,溶血磷脂酰基甘油和溶血磷脂苷肌醇的血浆水平,并且它在含含量的脂蛋白中增加了它们的内容物,同时它在小鼠中降低了它们的HDL和脂蛋白耗尽级分中的含量。 LDL受体(LDLR)的过表达降低了溶血磷脂酰胆碱,溶血磷脂酰乙胺胺,溶血磷脂磷脂和溶血磷脂苷肌醇等血浆水平,并降低了LDL,HDL和脂蛋白耗尽的级分中这些化合物的内容物,而LDLR的敲低增加了它们。这些结果表明甘油 - 溶血磷脂在脂蛋白脂蛋白的热熵作用以及脂蛋白代谢在甘油 - 溶血磷脂调节中的重要性。

著录项

  • 来源
    《The Biochemical Journal》 |2019年第23期|共17页
  • 作者单位

    Univ Tokyo Dept Clin Lab Med Tokyo Japan;

    Tohoku Univ Grad Sch Pharmaceut Sci Lab Mol &

    Cellular Biochem Sendai Miyagi Japan;

    Teikyo Univ Mizonokuchi Hosp Sch Med Dept Med 4 Kawasaki Kanagawa Japan;

    Teikyo Univ Sch Med Dept Internal Med Tokyo Japan;

    Tohoku Univ Grad Sch Pharmaceut Sci Lab Mol &

    Cellular Biochem Sendai Miyagi Japan;

    Univ Tokyo Dept Clin Lab Med Tokyo Japan;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物化学;
  • 关键词

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号