Chair of Pharmacology, Jagiellonian University Medical College, Poland.
J Proteomics. 2011 May 16;74(6):887-93. doi: 10.1016/j.jprot.2011.03.003. Epub 2011 Mar 23.
The involvement of both apolipoprotein E (apoE) and mitochondria in lipid metabolism is widely recognized, however there is surprisingly scarce data about the putative mitochondrial action(s) of this protein. The aim of the study was to screen the alterations in liver mitochondrial proteome caused by apoE deficiency. We applied 2DE-LC-MS/MS methodology to investigate the changes in liver mitochondrial protein expression in 6-months old apoE(-/-) mice as compared to C57BL/6J controls. ApoE(-/-), but not C57BL/6J mice developed visible atherosclerotic changes in aorta and mild, diffuse steatosis of the liver. Collectively, 18 differentially expressed proteins were identified in mitochondria, related to apoptosis, antioxidant and detoxifying mechanisms of mitochondria, as well as lipid metabolism and transport. In conclusion, differential proteomic approach revealed several lines of proteomic evidence that mitochondrial function in the liver of apoE(-/-) mice could be altered as a result of overlapping of pathological and compensatory changes in expression of proteins.
载脂蛋白 E (apoE) 和线粒体都广泛参与脂质代谢,然而关于该蛋白在细胞器中的作用(多种作用)的数据却少之又少。本研究旨在筛选 apoE 缺乏导致的肝线粒体蛋白质组的改变。我们应用 2DE-LC-MS/MS 方法,比较了 6 月龄 apoE(-/-) 小鼠与 C57BL/6J 对照组之间肝线粒体蛋白表达的变化。结果显示,apoE(-/-)小鼠出现明显的主动脉粥样硬化改变,而 C57BL/6J 小鼠则出现轻度弥漫性肝脂肪变性。总的来说,在肝线粒体中鉴定到 18 个差异表达蛋白,与凋亡、抗氧化和细胞器解毒机制以及脂质代谢和转运有关。结论:差异蛋白质组学方法揭示了一些蛋白质组学证据,apoE(-/-) 小鼠肝脏线粒体功能可能发生改变,这是由于病理和代偿性改变导致蛋白表达重叠的结果。