Walkey C J, Yu L, Agellon L B, Vance D E
Lipid and Lipoprotein Research Group and the Department of Biochemistry, University of Alberta, Edmonton, Alberta T6G 2S2, Canada.
J Biol Chem. 1998 Oct 16;273(42):27043-6. doi: 10.1074/jbc.273.42.27043.
All nucleated mammalian cells synthesize phosphatidylcholine from choline via the CDP-choline pathway. Hepatocytes have a second pathway for the synthesis of phosphatidylcholine, a stepwise methylation of phosphatidylethanolamine, catalyzed by phosphatidylethanolamine N-methyltransferase and encoded by the Pempt gene. We report that when Pempt-deficient mice were fed a choline-deficient diet for 3 days, severe liver pathology occurred apparently due to a lack of phosphatidylcholine biosynthesis. The hepatic concentration of phosphatidylcholine decreased by 50% compared with wild type mice on the diet. The levels of plasma triacylglycerols and cholesterol were decreased by greater than 90% in the Pempt-deficient mice. We suggest that the Pempt gene has been maintained during evolution to provide phosphatidylcholine when dietary choline is insufficient, as might occur during starvation or pregnancy.
所有有核哺乳动物细胞都通过CDP-胆碱途径从胆碱合成磷脂酰胆碱。肝细胞有另一条合成磷脂酰胆碱的途径,即磷脂酰乙醇胺的逐步甲基化,由磷脂酰乙醇胺N-甲基转移酶催化,该酶由Pempt基因编码。我们报告,当给Pempt基因缺陷小鼠喂食缺乏胆碱的饮食3天时,明显出现了严重的肝脏病变,这显然是由于缺乏磷脂酰胆碱生物合成所致。与喂食该饮食的野生型小鼠相比,肝脏中磷脂酰胆碱的浓度降低了50%。Pempt基因缺陷小鼠血浆中的三酰甘油和胆固醇水平降低了90%以上。我们认为,在进化过程中保留了Pempt基因,以便在膳食胆碱不足时(如在饥饿或怀孕期间可能发生的情况)提供磷脂酰胆碱。