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趋化因子配体5(CXCL5)会导致肥胖,进而引发糖尿病,甚至更严重的后果。

CXCL5 drives obesity to diabetes, and further.

作者信息

Chavey Carine, Fajas Lluis

机构信息

IRCM, Institut de Recherche en Cancérologie de Montpellier, Montpellier, F-34298, France.

出版信息

Aging (Albany NY). 2009 Jul 2;1(7):674-7. doi: 10.18632/aging.100064.

Abstract

We have recently shown that the CXCL5 chemokine is secreted by adipose tissue in the obese state. We demonstrated that adipose tissue-derived CXCL5 mediates insulin resistance in muscle. We speculate in this paper that CXCL5 could also mediate other obesity, and diabetes-derived pathologies, such as cardiovascular disease, retinopathy, or inflammatory bowel disease. In this scenario CXCL5 targeted therapy would prevent not only the development of type II diabetes in obese subjects, but also several other obesity-related co morbidities. Finally we propose to analyze the CXCL5 gene to find particular polymorphisms that could predict the development of type II diabetes in obese subjects.

摘要

我们最近发现,肥胖状态下的脂肪组织会分泌CXCL5趋化因子。我们证明,脂肪组织来源的CXCL5可介导肌肉中的胰岛素抵抗。在本文中,我们推测CXCL5也可能介导其他肥胖及糖尿病相关病症,如心血管疾病、视网膜病变或炎症性肠病。在这种情况下,CXCL5靶向治疗不仅可以预防肥胖受试者患II型糖尿病,还可以预防其他几种与肥胖相关的合并症。最后,我们建议分析CXCL5基因,以寻找可预测肥胖受试者患II型糖尿病的特定多态性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f9b/2806041/12160b9d4c6f/aging-01-674-g001.jpg

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