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Midkine, a Potential Link between Obesity and Insulin Resistance
Author(s) -
Nengguang Fan,
Haiyan Sun,
Yifei Wang,
Lijuan Zhang,
Zhenhua Xia,
Liang Peng,
Yanqiang Hou,
Weiqin Shen,
Rui Liu,
Yongde Peng
Publication year - 2014
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0088299
Subject(s) - insulin resistance , medicine , endocrinology , glut4 , socs3 , adipose tissue , adipocyte , insulin receptor , insulin , protein kinase b , fgf21 , adipogenesis , midkine , irs1 , proinflammatory cytokine , glucose transporter , biology , signal transduction , inflammation , growth factor , microbiology and biotechnology , fibroblast growth factor , receptor , cancer , suppressor
Obesity is associated with increased production of inflammatory mediators in adipose tissue, which contributes to chronic inflammation and insulin resistance. Midkine (MK) is a heparin-binding growth factor with potent proinflammatory activities. We aimed to test whether MK is associated with obesity and has a role in insulin resistance. It was found that MK was expressed in adipocytes and regulated by inflammatory modulators (TNF-α and rosiglitazone). In addition, a significant increase in MK levels was observed in adipose tissue of obese ob/ob mice as well as in serum of overweight/obese subjects when compared with their respective controls. In vitro studies further revealed that MK impaired insulin signaling in 3T3-L1 adipocytes, as indicated by reduced phosphorylation of Akt and IRS-1 and decreased translocation of glucose transporter 4 (GLUT4) to the plasma membrane in response to insulin stimulation. Moreover, MK activated the STAT3-suppressor of cytokine signaling 3 (SOCS3) pathway in adipocytes. Thus, MK is a novel adipocyte-secreted factor associated with obesity and inhibition of insulin signaling in adipocytes. It may provide a potential link between obesity and insulin resistance.

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