Boehringer Ingelheim Pharma GmbH & Co. KG, Biberach an der Riss, Germany.
J Neurol Sci. 2010 Aug 15;295(1-2):46-52. doi: 10.1016/j.jns.2010.05.013. Epub 2010 Jun 8.
Point mutations in the mitochondrial genome are associated with a variety of metabolic disorders. The myopathy, encephalopathy, lactic acidosis, stroke-like episodes syndrome (MELAS), is most frequently associated with an A to G transition at position 3243 of the mitochondrial tRNA(Leu(UUR)) gene, and is characterized by biochemical and structural alterations of mitochondria. In the present study, we analyzed proteomic changes in an immortalized B-cell line harbouring the MELAS A3243G mutation by two-dimensional difference gel electrophoresis and immunoblot analysis. Although the cell line contained only 10% mutated mitochondrial genomes, we detected significant alterations in numerous proteins associated with the actin cytoskeleton and in nuclear-encoded subunits of mitochondrial respiratory chain complexes. Notably, mitochondrial Lon protease and Hsp60 were deregulated in MELAS cells, indicating an effect on the mitochondrial protein quality control system. By immunofluorescence microscopy, we detected mitochondrial Lon protease accumulation and changes in actin-binding proteins preferentially in MELAS cells containing numerous mitochondria with mutated genomes. Enzymatic assays revealed that Lon protease activity is increased in MELAS cell lysates. Although Lon protease has been shown to degrade misfolded proteins and to stabilize respiratory chain complexes within mitochondria, our MELAS cell line exhibited a higher sensitivity to mitochondrial stress. These findings provide novel insights into the cellular response to dysfunctional mitochondria containing mutated genomes.
线粒体基因组点突变与多种代谢紊乱有关。肌病、脑病、乳酸酸中毒、卒中样发作综合征(MELAS)最常与线粒体 tRNA(Leu(UUR))基因 3243 位的 A 到 G 转换有关,其特征是线粒体的生化和结构改变。在本研究中,我们通过二维差异凝胶电泳和免疫印迹分析,分析了携带 MELAS A3243G 突变的永生化 B 细胞系中的蛋白质组变化。尽管该细胞系仅含有 10%的突变线粒体基因组,但我们检测到与肌动蛋白细胞骨架相关的许多蛋白质以及线粒体呼吸链复合物的核编码亚基发生了显著改变。值得注意的是,MELAS 细胞中线粒体 Lon 蛋白酶和 Hsp60 失调,表明对线粒体蛋白质量控制系统有影响。通过免疫荧光显微镜,我们检测到线粒体 Lon 蛋白酶在含有大量突变基因组线粒体的 MELAS 细胞中积累和肌动蛋白结合蛋白发生变化。酶促测定显示 Lon 蛋白酶活性在 MELAS 细胞裂解物中增加。尽管 Lon 蛋白酶已被证明可降解错误折叠的蛋白质并稳定线粒体内的呼吸链复合物,但我们的 MELAS 细胞系对线粒体应激的敏感性更高。这些发现为了解含有突变基因组的功能失调线粒体的细胞反应提供了新的见解。