共 49 条
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
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机构:
Univ Tokyo, Grad Sch Med, Dept Diabet & Metab Dis, Tokyo 1138655, Japan Univ Tokyo, Grad Sch Med, Dept Diabet & Metab Dis, Tokyo 1138655, Japan

Ueki, Kohjiro
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机构:
Univ Tokyo, Grad Sch Med, Dept Diabet & Metab Dis, Tokyo 1138655, Japan
Univ Tokyo, TSBMI, Tokyo 1138655, Japan Univ Tokyo, Grad Sch Med, Dept Diabet & Metab Dis, Tokyo 1138655, Japan

Inabe, Kazunori
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h-index: 0
机构:
Univ Tokyo, Grad Sch Med, Dept Diabet & Metab Dis, Tokyo 1138655, Japan Univ Tokyo, Grad Sch Med, Dept Diabet & Metab Dis, Tokyo 1138655, Japan

Yamauchi, Toshimasa
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Univ Tokyo, Grad Sch Med, Dept Diabet & Metab Dis, Tokyo 1138655, Japan Univ Tokyo, Grad Sch Med, Dept Diabet & Metab Dis, Tokyo 1138655, Japan

Kubota, Naoto
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Univ Tokyo, Grad Sch Med, Dept Diabet & Metab Dis, Tokyo 1138655, Japan
Univ Tokyo, TSBMI, Tokyo 1138655, Japan
Natl Inst Hlth & Nutr, Clin Nutr Program, Tokyo 1628636, Japan Univ Tokyo, Grad Sch Med, Dept Diabet & Metab Dis, Tokyo 1138655, Japan

Kaneko, Kazuma
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Univ Tokyo, Grad Sch Med, Dept Diabet & Metab Dis, Tokyo 1138655, Japan Univ Tokyo, Grad Sch Med, Dept Diabet & Metab Dis, Tokyo 1138655, Japan

Kobayashi, Masatoshi
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Univ Tokyo, Grad Sch Med, Dept Diabet & Metab Dis, Tokyo 1138655, Japan Univ Tokyo, Grad Sch Med, Dept Diabet & Metab Dis, Tokyo 1138655, Japan

Iwane, Aya
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Univ Tokyo, Grad Sch Med, Dept Diabet & Metab Dis, Tokyo 1138655, Japan Univ Tokyo, Grad Sch Med, Dept Diabet & Metab Dis, Tokyo 1138655, Japan

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Okazaki, Yukiko
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Univ Tokyo, Grad Sch Med, Dept Diabet & Metab Dis, Tokyo 1138655, Japan Univ Tokyo, Grad Sch Med, Dept Diabet & Metab Dis, Tokyo 1138655, Japan

Ohsugi, Mitsuru
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Univ Tokyo, Grad Sch Med, Dept Diabet & Metab Dis, Tokyo 1138655, Japan Univ Tokyo, Grad Sch Med, Dept Diabet & Metab Dis, Tokyo 1138655, Japan

Takamoto, Iseki
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Univ Tokyo, Grad Sch Med, Dept Diabet & Metab Dis, Tokyo 1138655, Japan Univ Tokyo, Grad Sch Med, Dept Diabet & Metab Dis, Tokyo 1138655, Japan

Yamashita, Satoshi
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机构:
Natl Res Inst Child Hlth & Dev, Dept Syst BioMed, Tokyo 1578535, Japan Univ Tokyo, Grad Sch Med, Dept Diabet & Metab Dis, Tokyo 1138655, Japan

Asahara, Hiroshi
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机构:
Natl Res Inst Child Hlth & Dev, Dept Syst BioMed, Tokyo 1578535, Japan Univ Tokyo, Grad Sch Med, Dept Diabet & Metab Dis, Tokyo 1138655, Japan

Akira, Shizuo
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h-index: 0
机构:
Osaka Univ, WPI Immunol Frontier Res Ctr, Host Def Lab, Suita, Osaka 5650871, Japan Univ Tokyo, Grad Sch Med, Dept Diabet & Metab Dis, Tokyo 1138655, Japan

Kasuga, Masato
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机构:
Int Med Ctr Japan, Res Inst, Tokyo 1620052, Japan Univ Tokyo, Grad Sch Med, Dept Diabet & Metab Dis, Tokyo 1138655, Japan

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h-index:
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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.
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收藏
页码:401 / 412
页数:12
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