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Mitochondrial adaptation in steatotic mice.
Einer, Claudia; Hohenester, Simon; Wimmer, Ralf; Wottke, Lena; Artmann, Renate; Schulz, Sabine; Gosmann, Christian; Simmons, Alisha; Leitzinger, Christin; Eberhagen, Carola; Borchard, Sabine; Schmitt, Sabine; Hauck, Stefanie M; von Toerne, Christine; Jastroch, Martin; Walheim, Ellen; Rust, Christian; Gerbes, Alexander L; Popper, Bastian; Mayr, Doris; Schnurr, Max; Vollmar, Angelika M; Denk, Gerald; Zischka, Hans.
Affiliation
  • Einer C; Institute of Molecular Toxicology and Pharmacology, Helmholtz Center Munich, German Research Center for Environmental Health, 85764 Neuherberg, Germany.
  • Hohenester S; Department of Medicine II, Liver Center Munich, University Hospital LMU Munich, 81377 Munich, Germany.
  • Wimmer R; Department of Medicine II, Liver Center Munich, University Hospital LMU Munich, 81377 Munich, Germany.
  • Wottke L; Department of Medicine II, Liver Center Munich, University Hospital LMU Munich, 81377 Munich, Germany.
  • Artmann R; Department of Medicine II, Liver Center Munich, University Hospital LMU Munich, 81377 Munich, Germany.
  • Schulz S; Institute of Molecular Toxicology and Pharmacology, Helmholtz Center Munich, German Research Center for Environmental Health, 85764 Neuherberg, Germany.
  • Gosmann C; Institute of Molecular Toxicology and Pharmacology, Helmholtz Center Munich, German Research Center for Environmental Health, 85764 Neuherberg, Germany.
  • Simmons A; Institute of Molecular Toxicology and Pharmacology, Helmholtz Center Munich, German Research Center for Environmental Health, 85764 Neuherberg, Germany.
  • Leitzinger C; Institute of Molecular Toxicology and Pharmacology, Helmholtz Center Munich, German Research Center for Environmental Health, 85764 Neuherberg, Germany.
  • Eberhagen C; Institute of Molecular Toxicology and Pharmacology, Helmholtz Center Munich, German Research Center for Environmental Health, 85764 Neuherberg, Germany.
  • Borchard S; Institute of Molecular Toxicology and Pharmacology, Helmholtz Center Munich, German Research Center for Environmental Health, 85764 Neuherberg, Germany.
  • Schmitt S; Institute of Toxicology and Environmental Hygiene, Technical University of Munich, 80802 Munich, Germany.
  • Hauck SM; Research Unit Protein Science, Helmholtz Center Munich, German Research Center for Environmental Health, 85764 Neuherberg, Germany.
  • von Toerne C; Research Unit Protein Science, Helmholtz Center Munich, German Research Center for Environmental Health, 85764 Neuherberg, Germany.
  • Jastroch M; Institute of Diabetes and Obesity, Helmholtz Center Munich, German Research Center for Environmental Health, 85764 Neuherberg, Germany.
  • Walheim E; Institute of Diabetes and Obesity, Helmholtz Center Munich, German Research Center for Environmental Health, 85764 Neuherberg, Germany.
  • Rust C; Department of Medicine I, Krankenhaus Barmherzige Brüder, 80639 Munich, Germany.
  • Gerbes AL; Department of Medicine II, Liver Center Munich, University Hospital LMU Munich, 81377 Munich, Germany.
  • Popper B; Biomedical Center, Department of Anatomy and Cell biology, LMU Munich, 82152, Planegg-Martinsried, Germany.
  • Mayr D; Department of Pathology, LMU Munich, 80337 Munich, Germany.
  • Schnurr M; Division of Clinical Pharmacology & Center for Integrated Protein Science Munich (CIPSM), Klinikum der Universität München, 80337 Munich, Germany.
  • Vollmar AM; Department of Pharmacy, Center for Drug Research, Pharmaceutical Biology, LMU Munich, 81377 Munich, Germany.
  • Denk G; Department of Medicine II, Liver Center Munich, University Hospital LMU Munich, 81377 Munich, Germany.
  • Zischka H; Institute of Molecular Toxicology and Pharmacology, Helmholtz Center Munich, German Research Center for Environmental Health, 85764 Neuherberg, Germany; Institute of Toxicology and Environmental Hygiene, Technical University of Munich, 80802 Munich, Germany. Electronic address: zischka@helmholtz-mue
Mitochondrion ; 40: 1-12, 2018 05.
Article in En | MEDLINE | ID: mdl-28935446
ABSTRACT
Western lifestyle-associated malnutrition causes steatosis that may progress to liver inflammation and mitochondrial dysfunction has been suggested as a key factor in promoting this disease. Here we have molecularly, biochemically and biophysically analyzed mitochondria from steatotic wild type and immune-compromised mice fed a Western diet (WD) - enriched in saturated fatty acids (SFAs). WD-mitochondria demonstrated lipidomic changes, a decreased mitochondrial ATP production capacity and a significant sensitivity to calcium. These changes preceded hepatocyte damage and were not associated with enhanced ROS production. Thus, WD-mitochondria do not promote steatohepatitis per se, but demonstrate bioenergetic deficits and increased sensitivity to stress signals.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hepatocytes / Fatty Liver / Mitochondria Type of study: Prognostic_studies Limits: Animals Language: En Journal: Mitochondrion Year: 2018 Document type: Article Affiliation country: Germany

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hepatocytes / Fatty Liver / Mitochondria Type of study: Prognostic_studies Limits: Animals Language: En Journal: Mitochondrion Year: 2018 Document type: Article Affiliation country: Germany