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一种人源化骨桥蛋白小鼠模型及其在免疫代谢性肥胖研究中的应用。

A humanized osteopontin mouse model and its application in immunometabolic obesity studies.

作者信息

Grün Nicole G, Zeyda Karina, Moreno-Viedma Veronica, Strohmeier Karin, Staffler Günther, Zeyda Maximilian, Stulnig Thomas M

机构信息

Christian Doppler Laboratory for Cardio-Metabolic Immunotherapy and Clinical Division of Endocrinology and Metabolism, Department of Medicine III, Medical University of Vienna, Vienna, Austria.

Christian Doppler Laboratory for Cardio-Metabolic Immunotherapy and Clinical Division of Endocrinology and Metabolism, Department of Medicine III, Medical University of Vienna, Vienna, Austria; FH Campus Wien, University of Applied Sciences, Department Health, Section Biomedical Science, Vienna, Austria.

出版信息

Transl Res. 2016 Dec;178:63-73.e2. doi: 10.1016/j.trsl.2016.07.009. Epub 2016 Jul 18.

Abstract

Osteopontin (OPN) is a multifunctional protein involved in several inflammatory processes and pathogeneses including obesity-related disorders and cancer. OPN binds to a variety of integrin receptors and CD44 resulting in a proinflammatory stimulus. Therefore, OPN constitutes a novel interesting target to develop new therapeutic strategies, which counteract OPN's proinflammatory properties. We established a humanized SPP1 (hSPP1) mouse model and evaluated its suitability as a model for obesity and insulin resistance. Unchallenged hSPP1 animals did not significantly differ in body weight and gross behavioral properties compared to wild-type (WT) animals. High-fat diet-challenged hSPP1 similarly developed obesity and inflammation, whereas insulin resistance was markedly changed. However, OPN expression profile in tissues was significantly altered in hSPP1 compared to WT depending on the diet. In conclusion, we developed a versatile humanized model to study the action of OPN in vivo and to develop strategies that target human OPN in a variety of pathologies.

摘要

骨桥蛋白(OPN)是一种多功能蛋白质,参与多种炎症过程和发病机制,包括与肥胖相关的疾病和癌症。OPN与多种整合素受体和CD44结合,产生促炎刺激。因此,OPN构成了一个开发新治疗策略的有趣新靶点,这些策略可抵消OPN的促炎特性。我们建立了一种人源化SPP1(hSPP1)小鼠模型,并评估了其作为肥胖和胰岛素抵抗模型的适用性。与野生型(WT)动物相比,未经刺激的hSPP1动物在体重和总体行为特性方面没有显著差异。高脂饮食刺激的hSPP1同样会发生肥胖和炎症,而胰岛素抵抗则有明显变化。然而,与WT相比,hSPP1中组织中的OPN表达谱根据饮食情况有显著改变。总之,我们开发了一种通用的人源化模型,用于研究OPN在体内的作用,并制定针对多种病理情况下人OPN的策略。

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