Adiponectin Enhances Insulin Sensitivity by Increasing Hepatic IRS-2 Expression via a Macrophage-Derived IL-6-Dependent Pathway

被引:250
作者
Awazawa, Motoharu [1 ]
Ueki, Kohjiro [1 ,2 ]
Inabe, Kazunori [1 ]
Yamauchi, Toshimasa [1 ]
Kubota, Naoto [1 ,2 ,3 ]
Kaneko, Kazuma [1 ]
Kobayashi, Masatoshi [1 ]
Iwane, Aya [1 ]
Sasako, Takayoshi [1 ]
Okazaki, Yukiko [1 ]
Ohsugi, Mitsuru [1 ]
Takamoto, Iseki [1 ]
Yamashita, Satoshi [4 ]
Asahara, Hiroshi [4 ]
Akira, Shizuo [5 ]
Kasuga, Masato [6 ]
Kadowaki, Takashi [1 ,2 ]
机构
[1] Univ Tokyo, Grad Sch Med, Dept Diabet & Metab Dis, Tokyo 1138655, Japan
[2] Univ Tokyo, TSBMI, Tokyo 1138655, Japan
[3] Natl Inst Hlth & Nutr, Clin Nutr Program, Tokyo 1628636, Japan
[4] Natl Res Inst Child Hlth & Dev, Dept Syst BioMed, Tokyo 1578535, Japan
[5] Osaka Univ, WPI Immunol Frontier Res Ctr, Host Def Lab, Suita, Osaka 5650871, Japan
[6] Int Med Ctr Japan, Res Inst, Tokyo 1620052, Japan
关键词
COMPLEMENT-RELATED PROTEIN; HIGH-MOLECULAR-WEIGHT; FATTY-ACID OXIDATION; C-REACTIVE PROTEIN; ADIPOSE-TISSUE; T-CADHERIN; KAPPA-B; GLOBULAR ADIPONECTIN; RECEPTOR SUBSTRATE-1; GLUCOSE-HOMEOSTASIS;
D O I
10.1016/j.cmet.2011.02.010
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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 alpha (PPAR alpha). 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 NF kappa B 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.
引用
收藏
页码:401 / 412
页数:12
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