Midkine, a potential link between obesity and insulin resistance.

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 obesit...

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Main Authors: Nengguang Fan, Haiyan Sun, Yifei Wang, Lijuan Zhang, Zhenhua Xia, Liang Peng, Yanqiang Hou, Weiqin Shen, Rui Liu, Yongde Peng
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3917881?pdf=render
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spelling doaj-02afbf7570fa462d8c6654306a25b6cb2020-11-25T00:12:41ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0192e8829910.1371/journal.pone.0088299Midkine, a potential link between obesity and insulin resistance.Nengguang FanHaiyan SunYifei WangLijuan ZhangZhenhua XiaLiang PengYanqiang HouWeiqin ShenRui LiuYongde PengObesity 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.http://europepmc.org/articles/PMC3917881?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Nengguang Fan
Haiyan Sun
Yifei Wang
Lijuan Zhang
Zhenhua Xia
Liang Peng
Yanqiang Hou
Weiqin Shen
Rui Liu
Yongde Peng
spellingShingle Nengguang Fan
Haiyan Sun
Yifei Wang
Lijuan Zhang
Zhenhua Xia
Liang Peng
Yanqiang Hou
Weiqin Shen
Rui Liu
Yongde Peng
Midkine, a potential link between obesity and insulin resistance.
PLoS ONE
author_facet Nengguang Fan
Haiyan Sun
Yifei Wang
Lijuan Zhang
Zhenhua Xia
Liang Peng
Yanqiang Hou
Weiqin Shen
Rui Liu
Yongde Peng
author_sort Nengguang Fan
title Midkine, a potential link between obesity and insulin resistance.
title_short Midkine, a potential link between obesity and insulin resistance.
title_full Midkine, a potential link between obesity and insulin resistance.
title_fullStr Midkine, a potential link between obesity and insulin resistance.
title_full_unstemmed Midkine, a potential link between obesity and insulin resistance.
title_sort midkine, a potential link between obesity and insulin resistance.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description 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.
url http://europepmc.org/articles/PMC3917881?pdf=render
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