Han Yingchun, Qi Rong, Liu George
Institute of Cardiovascular Sciences and Key Laboratory of Molecular Cardiovascular Sciences, Ministry of Education, Peking University Health Science Center, Beijing, 100191, China.
Institute of Cardiovascular Sciences and Key Laboratory of Molecular Cardiovascular Sciences, Ministry of Education, Peking University Health Science Center, Beijing, 100191, China.
Biochem Biophys Res Commun. 2015 Jul 10;462(4):420-5. doi: 10.1016/j.bbrc.2015.04.147. Epub 2015 May 9.
Clinical and epidemiological investigations confirm that patients with loss-of-function mutations (R19X, etc.) in Apolipoprotein CIII (ApoCIII) showed beneficial lipid profile including decreased plasma triglyceride and increased high density lipoprotein (HDL) levels. However, whether HDL level would be reduced in hypertriglyceridemia (HTG) induced by high ApoCIII expression has not been demonstrated yet. Here we showed, ApoCIII transgenic mice (ApoCIIItg) displayed severe HTG and had significantly lower HDL level. Analysis of apolipoproteins in lipoprotein fractions by SDS-PAGE revealed marked decrease of apolipoprotein AI (ApoAI) in HDL in transgenic mice compared with the wild type mice (WT) as controls. Further examination demonstrated that hepatic but not intestinal ApoAI mRNA was significantly reduced. Therefore, the decreased ApoAI synthesis might be accounted for the lower plasma HDL level in ApoCIII transgenic mice.
临床和流行病学调查证实,载脂蛋白CIII(ApoCIII)功能丧失突变(如R19X等)的患者表现出有益的血脂谱,包括血浆甘油三酯降低和高密度脂蛋白(HDL)水平升高。然而,高ApoCIII表达诱导的高甘油三酯血症(HTG)中HDL水平是否会降低尚未得到证实。在此我们发现,ApoCIII转基因小鼠(ApoCIIItg)表现出严重的HTG,且HDL水平显著降低。通过SDS-PAGE对脂蛋白组分中的载脂蛋白进行分析发现,与作为对照的野生型小鼠(WT)相比,转基因小鼠HDL中的载脂蛋白AI(ApoAI)明显减少。进一步检查表明,肝脏而非肠道的ApoAI mRNA显著降低。因此,ApoAI合成减少可能是ApoCIII转基因小鼠血浆HDL水平较低的原因。