| Literature DB >> 21459325 |
Motoharu Awazawa1, Kohjiro Ueki2, Kazunori Inabe1, Toshimasa Yamauchi1, Naoto Kubota3, Kazuma Kaneko1, Masatoshi Kobayashi1, Aya Iwane1, Takayoshi Sasako1, Yukiko Okazaki1, Mitsuru Ohsugi1, Iseki Takamoto1, Satoshi Yamashita4, Hiroshi Asahara4, Shizuo Akira5, Masato Kasuga6, Takashi Kadowaki7.
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.Entities:
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Year: 2011 PMID: 21459325 DOI: 10.1016/j.cmet.2011.02.010
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287