日本語
 
Help Privacy Policy ポリシー/免責事項
  詳細検索ブラウズ

アイテム詳細


公開

学術論文

Heme Oxygenase-1 Drives Metaflammation and Insulin Resistance in Mouse and Man

MPS-Authors
/persons/resource/persons198938

Jais,  Alexander
Department of Epigenetics, Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society;

Einwallner,  Elisa
Max Planck Society;

/persons/resource/persons198926

Tsai-Hsiu Lu,  Tess
Department of Epigenetics, Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society;

/persons/resource/persons198939

Medgyesi,  David
Research Group and Chair of Molecular Immunology of the University of Freiburg, Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society;

/persons/resource/persons198924

Dalgaard,  Kevin
Department of Epigenetics, Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society;

/persons/resource/persons198873

Pospisilik,  J. Andrew
Department of Epigenetics, Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society;

External Resource
There are no locators available
Fulltext (restricted access)
There are currently no full texts shared for your IP range.
フルテキスト (公開)
公開されているフルテキストはありません
付随資料 (公開)
There is no public supplementary material available
引用

Jais, A., Einwallner, E., Sharif, O., Gossens, K., Tsai-Hsiu Lu, T., Soyal, S. M., Medgyesi, D., Neureiter, D., Paier-Pourani, J., Dalgaard, K., Duvigneau, J. C., Lindroos-Christensen, J., Zapf, T.-C., Amann, S., Saluzzo, S., Jantscher, F., Stiedl, P., Todoric, J., Martins, R., Oberkofler, H., Müller, S., Hauser-Kronberger, C., Kenner, L., Casanova, E., Sutterlüty-Fall, H., Bilban, M., Miller, K., Kozlov, A. V., Krempler, F., Knapp, S., Lumeng, C. N., Patsch, W., Wagner, O., Pospisilik, J. A., & Esterbauer, H. (2014). Heme Oxygenase-1 Drives Metaflammation and Insulin Resistance in Mouse and Man. Cell, 158, 25-40.


引用: https://hdl.handle.net/11858/00-001M-0000-002B-884B-D
要旨
Obesity and diabetes affect more than half a billion individuals worldwide. Interestingly, the two conditions do not always coincide and the molecular determinants of "healthy" versus "unhealthy" obesity remain ill-defined. Chronic metabolic inflammation (metaflammation) is believed to be pivotal. Here, we tested a hypothesized anti-inflammatory role for heme oxygenase-1 (HO-1) in the development of metabolic disease. Surprisingly, in matched biopsies from "healthy" versus insulin-resistant obese subjects we find HO-1 to be among the strongest positive predictors of metabolic disease in humans. We find that hepatocyte and macrophage conditional HO-1 deletion in mice evokes resistance to diet-induced insulin resistance and inflammation, dramatically reducing secondary disease such as steatosis and liver toxicity. Intriguingly, cellular assays show that HO-1 defines prestimulation thresholds for inflammatory skewing and NF-κB amplification in macrophages and for insulin signaling in hepatocytes. These findings identify HO-1 inhibition as a potential therapeutic strategy for metabolic disease.