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CXCL14增强脂肪细胞中胰岛素依赖的葡萄糖摄取,并与高脂饮食诱导的肥胖有关。

CXCL14 enhances insulin-dependent glucose uptake in adipocytes and is related to high-fat diet-induced obesity.

作者信息

Takahashi Michiko, Takahashi Yutaka, Takahashi Kenichi, Zolotaryov Fyodor N, Hong Kyoung Su, Iida Keiji, Okimura Yasuhiko, Kaji Hidesuke, Chihara Kazuo

机构信息

Division of Diabetes, Metabolism and Endocrinology, Department of Internal Medicine, Kobe University Graduate School of Medicine, 7-5-2, Kusunoki-cho, Chu-o-ku, Kobe 650-0017, Japan.

出版信息

Biochem Biophys Res Commun. 2007 Dec 28;364(4):1037-42. doi: 10.1016/j.bbrc.2007.10.120. Epub 2007 Oct 29.

Abstract

Accumulating evidence suggests an association between obesity and adipose tissue inflammation. Chemokines are involved in the regulation of inflammation status. Chemokine (C-X-C motif) ligand 14 (CXCL14) is known to be a chemoattractant for monocyte and dendritic cells. Recently, it was reported that CXCL14-deficient mice show resistance to high-fat diet-induced obesity. In this study, we identified CXCL14 as a growth hormone (GH)-induced gene in HepG2 hepatoma cells. Substantial in vivo expression of CXCL14 was detected in the adipose tissue and liver. Its expression and secretion were strikingly increased by insulin administration and high-fat diet. Intriguingly, incubation of 3T3-L1 adipocytes with CXCL14 stimulated insulin-dependent glucose uptake. Further, this effect was associated with enhanced insulin signaling. CXCL14 enhanced the insulin-induced tyrosine phosphorylation of insulin receptors and insulin receptor substrate-1. These results suggest that CXCL14 plays a causal role in high-fat diet-induced obesity.

摘要

越来越多的证据表明肥胖与脂肪组织炎症之间存在关联。趋化因子参与炎症状态的调节。趋化因子(C-X-C基序)配体14(CXCL14)已知是单核细胞和树突状细胞的趋化剂。最近,有报道称CXCL14缺陷型小鼠对高脂饮食诱导的肥胖具有抗性。在本研究中,我们确定CXCL14是HepG2肝癌细胞中生长激素(GH)诱导的基因。在脂肪组织和肝脏中检测到CXCL14在体内大量表达。胰岛素给药和高脂饮食显著增加了其表达和分泌。有趣的是,用CXCL14孵育3T3-L1脂肪细胞可刺激胰岛素依赖性葡萄糖摄取。此外,这种作用与增强的胰岛素信号传导有关。CXCL14增强了胰岛素诱导的胰岛素受体和胰岛素受体底物-1的酪氨酸磷酸化。这些结果表明CXCL14在高脂饮食诱导的肥胖中起因果作用。

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