首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Sarco(endo)plasmic reticulum Ca2+-ATPase 2b is a major regulator of endoplasmic reticulum stress and glucose homeostasis in obesity
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Sarco(endo)plasmic reticulum Ca2+-ATPase 2b is a major regulator of endoplasmic reticulum stress and glucose homeostasis in obesity

机译:sarco(内质网)质网Ca2 + -ATPase 2b是肥胖中内质网应激和葡萄糖稳态的主要调节剂

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摘要

Increased endoplasmic reticulum (ER) stress is one of the central mechanisms that lead to dysregulated metabolic homeostasis in obesity. It is thus crucial to understand the underpinnings of the mechanisms that lead to the development of ER stress. A high level of ER Ca2+ is imperative for maintenance of normal ER function and this high Ca2+ concentration of ER is maintained by sarco(endo)plasmic reticulum Ca2+-ATPase (SERCA). Here, we show that SERCA2b protein and mRNA levels are dramatically reduced in the liver of obese mice and restoration of SERCA2b in the liver of obese and diabetic mice alleviates ER stress, increases glucose tolerance, and significantly reduces the blood glucose levels. Furthermore, overexpression of SERCA2b in the liver of obese mice significantly reduces the lipogenic gene expression and the triglyceride content in the liver. Our results document the importance of SERCA2b in dysregulated glucose and lipid homeostasis in the liver of obese mice and suggest development of drugs to increase SERCA2b activity for treatment of type 2 diabetes and nonalcoholic steatohepatitis.
机译:内质网(ER)压力增加是导致肥胖患者体内代谢稳态失调的主要机制之一。因此,至关重要的是要了解导致内质网应激的机制的基础。维持正常的ER功能势在必行,而高水平的ER Ca 2 + 必不可少,肌浆网内膜Ca 2 + 的高浓度ER得以维持。 sup> 2 + -ATPase(SERCA)。在这里,我们显示肥胖小鼠肝脏中的SERCA2b蛋白和mRNA水平显着降低,肥胖和糖尿病小鼠肝脏中SERCA2b的恢复减轻了ER应激,增加了糖耐量,并显着降低了血糖水平。此外,肥胖小鼠肝脏中SERCA2b的过表达显着降低了脂肪形成基因的表达和肝脏中甘油三酯的含量。我们的结果证明了SERCA2b在肥胖小鼠肝脏中葡萄糖和脂质稳态失调中的重要性,并建议开发可增加SERCA2b活性的药物来治疗2型糖尿病和非酒精性脂肪性肝炎。

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