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半胱氨酸β-合成酶缺乏小鼠(同型胱氨酸血症/同型胱氨酸尿症的动物模型)脂肪肝和再生非脂肪肝的三酰甘油/磷脂分子种类谱分析。

Triacylglycerol/phospholipid molecular species profiling of fatty livers and regenerated non-fatty livers in cystathionine beta-synthase-deficient mice, an animal model for homocysteinemia/homocystinuria.

机构信息

Department of Metabolome, Graduate School of Medicine, The University of Tokyo, Tokyo, 113-0033, Japan.

出版信息

Anal Bioanal Chem. 2011 Jun;400(7):1853-63. doi: 10.1007/s00216-011-4703-2. Epub 2011 Feb 8.

Abstract

Fatty liver is one of the typical manifestations in homocysteinemia/homocystinuria patients and their genetic animal model, mice lacking cystathionine β-synthase (Cbs(-/-)). The vast majority of Cbs(-/-) die within 4 weeks after birth via yet unknown mechanisms, whereas a small portion survive to adulthood, escaping fatty degeneration of the liver during lactation periods, through regeneration. To investigate the molecular basis of such fatty changes, we analyzed lipid components in fatty livers of 2-week-old Cbs(-/-) and regenerated non-fatty livers of 8-week-old Cbs(-/-) survivors using a chip-based nanoESI (electrospray ionization)-MS system, which allows quantitative detection of triacylglycerol/phospholipid molecular species. Hepatic levels of all major triacylglycerol species were much higher in Cbs(-/-) than in wild-type mice at 2 weeks, although not at 8 weeks. Levels of some phospholipid species were either up- or downregulated in 2-week-old Cbs(-/-); e.g. saturated (16:0 and 18:0) or mono-unsaturated (16:1 and 18:1) fatty acids-containing phosphatidylcholine/phosphatidylethanolamine species were upregulated, while poly-unsaturated fatty acids-containing phosphatidylcholine (18:2-18:2 and 18:2-20:5), phosphatidylethanolamine (18:1-20:4), and phosphatidylinositol (18:0-20:4) were downregulated. Capillary electrophoresis-MS analysis identified high-level accumulation of S-adenosylmethionine and S-adenosylhomocysteine in fatty livers of 2-week-old Cbs(-/-) but much less in non-fatty livers of 8-week-old Cbs(-/-). Although hepatic S-adenosylmethionine/S-adenosylhomocysteine ratios were comparable between 2-week-old Cbs(-/-) and wild-type, global protein arginine methylation was disturbed in fatty livers of Cbs(-/-). Our results suggest that cellular signaling mediated by altered phospholipid contents might be involved in pathogenesis of fatty liver in Cbs(-/-).

摘要

脂肪肝是高半胱氨酸血症/高同型半胱氨酸尿症患者及其遗传动物模型——缺乏胱硫醚β-合酶(Cbs(-/-))的小鼠的典型表现之一。绝大多数 Cbs(-/-)在出生后 4 周内死于未知机制,而一小部分存活到成年期,通过再生逃避哺乳期的肝脂肪变性。为了研究这种脂肪变化的分子基础,我们使用基于芯片的纳升电喷雾电离(ESI)-MS 系统分析了 2 周龄 Cbs(-/-)脂肪肝和 8 周龄 Cbs(-/-)幸存者再生非脂肪肝中的脂质成分,该系统允许定量检测三酰甘油/磷脂分子种类。在 2 周龄时,Cbs(-/-)小鼠的所有主要三酰甘油种类的肝水平均高于野生型小鼠,尽管在 8 周龄时并非如此。在 2 周龄的 Cbs(-/-)中,一些磷脂种类的水平上调或下调;例如,含有饱和(16:0 和 18:0)或单不饱和(16:1 和 18:1)脂肪酸的磷脂酰胆碱/磷脂酰乙醇胺种类上调,而多不饱和脂肪酸含量较高的磷脂酰胆碱(18:2-18:2 和 18:2-20:5)、磷脂酰乙醇胺(18:1-20:4)和磷脂酰肌醇(18:0-20:4)下调。毛细管电泳-MS 分析表明,在 2 周龄 Cbs(-/-)的脂肪肝中,S-腺苷甲硫氨酸和 S-腺苷同型半胱氨酸的水平高度累积,但在 8 周龄 Cbs(-/-)的非脂肪肝中则少得多。尽管 2 周龄 Cbs(-/-)和野生型小鼠的肝 S-腺苷甲硫氨酸/S-腺苷同型半胱氨酸比值相当,但 Cbs(-/-)的脂肪肝中,整体蛋白质精氨酸甲基化受到干扰。我们的结果表明,受改变的磷脂含量介导的细胞信号可能参与 Cbs(-/-)脂肪肝的发病机制。

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