Dose Janina, Nebel Almut, Piegholdt Stefanie, Rimbach Gerald, Huebbe Patricia
Institute of Human Nutrition and Food Science, University of Kiel, Hermann-Rodewald-Str. 6, 24118 Kiel, Germany.
Institute of Clinical Molecular Biology, University of Kiel, University Hospital Schleswig-Holstein, Schittenhelmstr. 12, 24105 Kiel, Germany.
Free Radic Biol Med. 2016 Jul;96:264-72. doi: 10.1016/j.freeradbiomed.2016.04.031. Epub 2016 Apr 26.
Apolipoprotein E (APOE) is a multifunctional plasma protein mainly acting in lipid metabolism. Human APOE is polymorphic with three major isoforms (APOE2, APOE3 and APOE4). Up to 75% of the body's APOE is produced by the liver. There is increasing evidence from studies in brain-derived cells that APOE4 affects mitochondrial function and biogenesis as well as stress and inflammatory responses - processes, whose disturbances are considered hallmarks of the ageing process. However, although the liver is the main production site of APOE, knowledge about the impact of the APOE genotype on hepatic stress response-related processes is rather limited. Therefore, we studied biomarkers of oxidative status (glutathione levels, 3-nitrotyrosine adducts, protein carbonyl concentration), ER stress (XBP1(S), BiP, DDIT3), proteasome activity, mitochondrial function (respiratory complexes, ATP levels and mitochondrial membrane potential as well as biomarkers of mitochondrial biogenesis, fission and fusion), autophagy (LC3, LAMP2A), apoptosis (BCL2, BAX, CYCS) and DNA damage in the liver of APOE targeted replacement (TR) mice and in Huh7 hepatocytes overexpressing the APOE3 and the APOE4 isoform, respectively. APOE4 mice exhibited a lower chymotrypsin-like and a higher trypsin-like proteasome activity. Levels of protein carbonyls were moderately higher in liver tissue of APOE4 vs. APOE3 mice. Other biomarkers of oxidative stress were similar between the two genotypes. Under basal conditions, the stress-response pathways investigated appeared largely unaffected by the APOE genotype. However, upon stress induction, APOE4 expressing cells showed lower levels of adenosine triphosphate (ATP) and lower mRNA levels of the ATP-generating complex V of the mitochondrial respiratory chain. Overall, our findings provide evidence for a rather low influence of the APOE genotype on the hepatic stress response processes investigated in this study.
载脂蛋白E(APOE)是一种主要参与脂质代谢的多功能血浆蛋白。人类APOE具有多态性,有三种主要异构体(APOE2、APOE3和APOE4)。人体高达75%的APOE由肝脏产生。来自脑源性细胞研究的证据越来越多,表明APOE4会影响线粒体功能和生物发生以及应激和炎症反应——这些过程的紊乱被认为是衰老过程的标志。然而,尽管肝脏是APOE的主要产生部位,但关于APOE基因型对肝脏应激反应相关过程影响的知识相当有限。因此,我们研究了氧化状态(谷胱甘肽水平、3-硝基酪氨酸加合物、蛋白质羰基浓度)、内质网应激(XBP1(S)、BiP、DDIT3)、蛋白酶体活性、线粒体功能(呼吸复合物、ATP水平和线粒体膜电位以及线粒体生物发生、裂变和融合的生物标志物)、自噬(LC3、LAMP2A)、凋亡(BCL2、BAX、CYCS)和DNA损伤的生物标志物,分别在APOE靶向替换(TR)小鼠的肝脏以及分别过表达APOE3和APOE4异构体的Huh7肝细胞中进行研究。APOE4小鼠表现出较低的胰凝乳蛋白酶样和较高的胰蛋白酶样蛋白酶体活性。与APOE3小鼠相比,APOE4小鼠肝脏组织中的蛋白质羰基水平略高。两种基因型之间氧化应激的其他生物标志物相似。在基础条件下,所研究的应激反应途径在很大程度上似乎不受APOE基因型的影响。然而,在应激诱导后,表达APOE4的细胞显示出较低的三磷酸腺苷(ATP)水平以及线粒体呼吸链中产生ATP的复合物V的较低mRNA水平。总体而言,我们的研究结果表明APOE基因型对本研究中所研究的肝脏应激反应过程影响较小。