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Adiponectin enhances insulin sensitivity by increasing hepatic IRS-2 expression via a macrophage-derived IL-6-dependent pathway.
Awazawa, Motoharu; Ueki, Kohjiro; Inabe, Kazunori; Yamauchi, Toshimasa; Kubota, Naoto; Kaneko, Kazuma; Kobayashi, Masatoshi; Iwane, Aya; Sasako, Takayoshi; Okazaki, Yukiko; Ohsugi, Mitsuru; Takamoto, Iseki; Yamashita, Satoshi; Asahara, Hiroshi; Akira, Shizuo; Kasuga, Masato; Kadowaki, Takashi.
Afiliación
  • Awazawa M; Department of Diabetes and Metabolic Diseases, Graduate School of Medicine, University of Tokyo, Tokyo 113-8655, Japan.
  • Ueki K; Department of Diabetes and Metabolic Diseases, Graduate School of Medicine, University of Tokyo, Tokyo 113-8655, Japan; Translational Systems Biology and Medicine Initiative (TSBMI), University of Tokyo, Tokyo 113-8655, Japan. Electronic address: ueki-tky@umin.ac.jp.
  • Inabe K; Department of Diabetes and Metabolic Diseases, Graduate School of Medicine, University of Tokyo, Tokyo 113-8655, Japan.
  • Yamauchi T; Department of Diabetes and Metabolic Diseases, Graduate School of Medicine, University of Tokyo, Tokyo 113-8655, Japan.
  • Kubota N; Department of Diabetes and Metabolic Diseases, Graduate School of Medicine, University of Tokyo, Tokyo 113-8655, Japan; Translational Systems Biology and Medicine Initiative (TSBMI), University of Tokyo, Tokyo 113-8655, Japan; Clinical Nutrition Program, National Institute of Health and Nutrition, T
  • Kaneko K; Department of Diabetes and Metabolic Diseases, Graduate School of Medicine, University of Tokyo, Tokyo 113-8655, Japan.
  • Kobayashi M; Department of Diabetes and Metabolic Diseases, Graduate School of Medicine, University of Tokyo, Tokyo 113-8655, Japan.
  • Iwane A; Department of Diabetes and Metabolic Diseases, Graduate School of Medicine, University of Tokyo, Tokyo 113-8655, Japan.
  • Sasako T; Department of Diabetes and Metabolic Diseases, Graduate School of Medicine, University of Tokyo, Tokyo 113-8655, Japan.
  • Okazaki Y; Department of Diabetes and Metabolic Diseases, Graduate School of Medicine, University of Tokyo, Tokyo 113-8655, Japan.
  • Ohsugi M; Department of Diabetes and Metabolic Diseases, Graduate School of Medicine, University of Tokyo, Tokyo 113-8655, Japan.
  • Takamoto I; Department of Diabetes and Metabolic Diseases, Graduate School of Medicine, University of Tokyo, Tokyo 113-8655, Japan.
  • Yamashita S; Department of Systems BioMedicine, National Research Institute of Child Health and Development, Tokyo 157-8535, Japan.
  • Asahara H; Department of Systems BioMedicine, National Research Institute of Child Health and Development, Tokyo 157-8535, Japan.
  • Akira S; Laboratory of Host Defense, WPI Immunology Frontier Research Center, Osaka University, Osaka 565-0871, Japan.
  • Kasuga M; Research Institute, International Medical Center of Japan, Tokyo 162-0052, Japan.
  • Kadowaki T; Department of Diabetes and Metabolic Diseases, Graduate School of Medicine, University of Tokyo, Tokyo 113-8655, Japan; Translational Systems Biology and Medicine Initiative (TSBMI), University of Tokyo, Tokyo 113-8655, Japan. Electronic address: kadowaki-3im@h.u-tokyo.ac.jp.
Cell Metab ; 13(4): 401-412, 2011 Apr 06.
Article en En | MEDLINE | ID: mdl-21459325
ABSTRACT
Insulin resistance is often associated with impeded insulin signaling due either to decreased concentrations or functional modifications of crucial signaling molecules including insulin receptor substrates (IRS) in the liver. Many actions of adiponectin, a well-recognized antidiabetic adipokine, are currently attributed to the activation of two critical molecules downstream of AdipoR1 and R2 AMP-activated kinase (AMPK) and peroxisome proliferator-activated receptor α (PPARα). However, the direct effects of adiponectin on insulin signaling molecules remain poorly understood. We show here that adiponectin upregulates IRS-2 through activation of signal transducer and activator of transcription-3 (STAT3). Surprisingly, this activation is associated with IL-6 production from macrophages induced by adiponectin through NFκB activation independent of its authentic receptors, AdipoR1 and AdipoR2. These data have unraveled an insulin-sensitizing action initiated by adiponectin leading to upregulation of hepatic IRS-2 via an IL-6 dependent pathway through a still unidentified adiponectin receptor.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Interleucina-6 / Adiponectina / Proteínas Sustrato del Receptor de Insulina / Hígado / Macrófagos Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Animals Idioma: En Revista: Cell Metab Asunto de la revista: METABOLISMO Año: 2011 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Interleucina-6 / Adiponectina / Proteínas Sustrato del Receptor de Insulina / Hígado / Macrófagos Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Animals Idioma: En Revista: Cell Metab Asunto de la revista: METABOLISMO Año: 2011 Tipo del documento: Article País de afiliación: Japón