Vance J E, Stone S J, Faust J R
Lipid and Lipoprotein Research Group, University of Alberta, Edmonton, Canada.
Biochim Biophys Acta. 1997 Feb 18;1344(3):286-99. doi: 10.1016/s0005-2760(96)00153-1.
Endoplasmic reticulum-like membranes (MAM) that are associated with mitochondria have been implicated as intermediates in the import of lipids, particularly phosphatidylserine, from the endoplasmic reticulum to mitochondria (Vance, J.E. (1990) J. Biol. Chem. 265, 7248-7256; Shiao, Y.-J. et al. (1995) J. Biol. Chem. 270, 11190-11198). We have now examined further the role of MAM in lipid metabolism using the mnd/mnd mouse, a model for the human degenerative disease neuronal ceroid lipofuscinosis. The biochemical phenotype of the mnd/mnd mutant mouse (in which lipids and proteins accumulate abnormally in storage bodies in cells of affected tissues) suggested that the mutation might lead to impaired mitochondrial import of lipids and proteins as a result of a defective linkage between MAM and mitochondria. We, therefore, investigated the status of MAM and phospholipid metabolism in mnd/mnd mice livers. Separation of MAM from livers of older, but not younger, mnd/mnd mice was aberrant. In addition, the amount of the MAM-specific protein, phosphatidylethanolamine N-methyltransferase-2 (PEMT2), was greatly reduced in homogenates and MAM from livers of mnd/mnd mice of all ages, although PEMT2 mRNA abundance was normal. Moreover, PEMT activity in MAM from mnd/mnd mice was 60% less than in control mice. Activities of two additional phospholipid biosynthetic enzymes-CTP:phosphocholine cytidylyltransferase and phosphatidylserine synthase-were also reduced by > 50% in mnd/mnd microsomes. Radiolabeling experiments in hepatocytes indicated that neither the mitochondrial import nor the subsequent metabolism of phosphatidylserine was grossly affected in mnd/mnd mice. However, 3 proteins (cytochrome b5, NADH:cytochrome b5 reductase and mitochondrial F1Fzero-ATP synthase c subunit) which are normally present in mitochondria were partially redistributed to microsomes in mnd/mnd mouse liver. These studies indicate that MAM are defective in the mnd/mnd mutant mouse in which the biochemical phenotype includes an abnormal accumulation of lipids and proteins in storage bodies.
与线粒体相关的内质网样膜(MAM)被认为是脂质(尤其是磷脂酰丝氨酸)从内质网导入线粒体过程中的中间体(万斯,J.E.(1990年)《生物化学杂志》265卷,7248 - 7256页;肖,Y.-J.等人(1995年)《生物化学杂志》270卷,11190 - 11198页)。我们现在利用mnd/mnd小鼠(一种人类退行性疾病神经元蜡样脂褐质沉积症的模型)进一步研究了MAM在脂质代谢中的作用。mnd/mnd突变小鼠(在受影响组织的细胞中,脂质和蛋白质异常积聚在储存体中)的生化表型表明,该突变可能由于MAM与线粒体之间的连接缺陷而导致脂质和蛋白质的线粒体导入受损。因此,我们研究了mnd/mnd小鼠肝脏中MAM和磷脂代谢的状况。从年龄较大而非较年轻的mnd/mnd小鼠肝脏中分离出的MAM出现异常。此外,所有年龄段的mnd/mnd小鼠肝脏匀浆和MAM中,MAM特异性蛋白磷脂酰乙醇胺N - 甲基转移酶 - 2(PEMT2)的量大幅减少,尽管PEMT2 mRNA丰度正常。而且,mnd/mnd小鼠MAM中的PEMT活性比对照小鼠低60%。mnd/mnd微粒体中另外两种磷脂生物合成酶——CTP:磷酸胆碱胞苷转移酶和磷脂酰丝氨酸合酶的活性也降低了50%以上。肝细胞中的放射性标记实验表明,mnd/mnd小鼠中磷脂酰丝氨酸的线粒体导入及其后续代谢均未受到严重影响。然而,通常存在于线粒体中的3种蛋白质(细胞色素b5、NADH:细胞色素b5还原酶和线粒体F1F零 - ATP合酶c亚基)在mnd/mnd小鼠肝脏中部分重新分布到了微粒体中。这些研究表明,在mnd/mnd突变小鼠中MAM存在缺陷,其生化表型包括储存体中脂质和蛋白质的异常积聚。