Literature DB >> 27130033

Influence of the APOE genotype on hepatic stress response: Studies in APOE targeted replacement mice and human liver cells.

Janina Dose1, Almut Nebel2, Stefanie Piegholdt3, Gerald Rimbach4, Patricia Huebbe5.   

Abstract

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.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  ATP; Apolipoprotein E isoform; Apoptosis; Autophagy; Endoplasmic reticulum stress; Hepatocytes; Mitochondrial function; Proteasome activity

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Year:  2016        PMID: 27130033     DOI: 10.1016/j.freeradbiomed.2016.04.031

Source DB:  PubMed          Journal:  Free Radic Biol Med        ISSN: 0891-5849            Impact factor:   7.376


  3 in total

1.  The effect of dietary fish oil on weight gain and insulin sensitivity is dependent on APOE genotype in humanized targeted replacement mice.

Authors:  Kenna E Slim; David Vauzour; Noemi Tejera; Peter J Voshol; Aedin Cassidy; Anne Marie Minihane
Journal:  FASEB J       Date:  2016-11-28       Impact factor: 5.191

Review 2.  Functional diversity of apolipoprotein E: from subcellular localization to mitochondrial function.

Authors:  Johanna Rueter; Gerald Rimbach; Patricia Huebbe
Journal:  Cell Mol Life Sci       Date:  2022-08-26       Impact factor: 9.207

3.  Autocrine Effects of Brain Endothelial Cell-Produced Human Apolipoprotein E on Metabolism and Inflammation in vitro.

Authors:  Felecia M Marottoli; Troy N Trevino; Xue Geng; Zarema Arbieva; Pinal Kanabar; Mark Maienschein-Cline; James C Lee; Sarah E Lutz; Leon M Tai
Journal:  Front Cell Dev Biol       Date:  2021-06-10
  3 in total

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