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骨桥蛋白缺失通过损害小鼠脂肪组织基质重塑以及减少脂肪组织和肝脏中的炎症和纤维化,预防肥胖和肝脂肪变性的发生。

Osteopontin deletion prevents the development of obesity and hepatic steatosis via impaired adipose tissue matrix remodeling and reduced inflammation and fibrosis in adipose tissue and liver in mice.

作者信息

Lancha Andoni, Rodríguez Amaia, Catalán Victoria, Becerril Sara, Sáinz Neira, Ramírez Beatriz, Burrell María A, Salvador Javier, Frühbeck Gema, Gómez-Ambrosi Javier

机构信息

Metabolic Research Laboratory, Clínica Universidad de Navarra, Pamplona, Spain; CIBER Fisiopatología de la Obesidad y Nutrición (CIBERobn), Instituto de Salud Carlos III, Madrid, Spain.

Metabolic Research Laboratory, Clínica Universidad de Navarra, Pamplona, Spain.

出版信息

PLoS One. 2014 May 28;9(5):e98398. doi: 10.1371/journal.pone.0098398. eCollection 2014.

Abstract

Osteopontin (OPN) is a multifunctional extracellular matrix (ECM) protein involved in multiple physiological processes. OPN expression is dramatically increased in visceral adipose tissue in obesity and the lack of OPN protects against the development of insulin resistance and inflammation in mice. We sought to unravel the potential mechanisms involved in the beneficial effects of the absence of OPN. We analyzed the effect of the lack of OPN in the development of obesity and hepatic steatosis induced by a high-fat diet (HFD) using OPN-KO mice. OPN expression was upregulated in epididymal white adipose tissue (EWAT) and liver in wild type (WT) mice with HFD. OPN-KO mice had higher insulin sensitivity, lower body weight and fat mass with reduced adipose tissue ECM remodeling and reduced adipocyte size than WT mice under a HFD. Reduced MMP2 and MMP9 activity was involved in the decreased ECM remodeling. Crown-like structure number in EWAT as well as F4/80-positive cells and Emr1 expression in EWAT and liver increased with HFD, while OPN-deficiency blunted the increase. Moreover, our data show for the first time that OPN-KO under a HFD mice display reduced fibrosis in adipose tissue and liver, as well as reduced oxidative stress in adipose tissue. Gene expression of collagens Col1a1, Col6a1 and Col6a3 in EWAT and liver, as well as the profibrotic cytokine Tgfb1 in EWAT were increased with HFD, while OPN-deficiency prevented this increase. OPN deficiency prevented hepatic steatosis via reduction in the expression of molecules involved in the onset of fat accumulation such as Pparg, Srebf1, Fasn, Mogat1, Dgat2 and Cidec. Furthermore, OPN-KO mice exhibited higher body temperature and improved BAT function. The present data reveal novel mechanisms of OPN in the development of obesity, pointing out the inhibition of OPN as a promising target for the treatment of obesity and fatty liver.

摘要

骨桥蛋白(OPN)是一种多功能细胞外基质(ECM)蛋白,参与多种生理过程。肥胖时内脏脂肪组织中OPN表达显著增加,而缺乏OPN可保护小鼠免受胰岛素抵抗和炎症的发展。我们试图阐明缺乏OPN产生有益作用的潜在机制。我们使用OPN基因敲除(KO)小鼠分析了缺乏OPN对高脂饮食(HFD)诱导的肥胖和肝脂肪变性发展的影响。在高脂饮食的野生型(WT)小鼠中,附睾白色脂肪组织(EWAT)和肝脏中OPN表达上调。与高脂饮食下的WT小鼠相比,OPN-KO小鼠具有更高的胰岛素敏感性、更低的体重和脂肪量,脂肪组织ECM重塑减少,脂肪细胞尺寸减小。MMP2和MMP9活性降低与ECM重塑减少有关。随着高脂饮食,EWAT中的冠状结构数量以及EWAT和肝脏中F4/80阳性细胞和Emr1表达增加,而OPN缺乏减弱了这种增加。此外,我们的数据首次表明,高脂饮食下的OPN-KO小鼠脂肪组织和肝脏中的纤维化减少,脂肪组织中的氧化应激也减少。随着高脂饮食,EWAT和肝脏中胶原蛋白Col1a1、Col6a1和Col6a3的基因表达以及EWAT中促纤维化细胞因子Tgfb1增加,而OPN缺乏阻止了这种增加。OPN缺乏通过减少参与脂肪积累起始的分子如Pparg、Srebf1、Fasn、Mogat1、Dgat2和Cidec的表达来预防肝脂肪变性。此外,OPN-KO小鼠表现出更高的体温和改善的棕色脂肪组织(BAT)功能。目前的数据揭示了OPN在肥胖发展中的新机制,指出抑制OPN作为治疗肥胖和脂肪肝的有前景的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/674e/4037189/c155d541c130/pone.0098398.g001.jpg

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