Department of Physiology & Biophysics, National Defense Medical Center, Taipei, Taiwan, 114, Republic of China.
Institute of Preventive Medicine, National Defense Medical Center, New Taipei City, Taiwan, 114, Republic of China.
Cell Death Dis. 2018 May 1;9(5):525. doi: 10.1038/s41419-018-0596-8.
Grail is a crucial regulator of various biological processes, including the development of T-cell anergy, antiviral innate immune response, and cancer. However, the role of Grail in adipogenesis and obesity remains unclear. Here, we demonstrated that Grail knockdown in vitro leads to a decrease in PPARγ expression, resulting in adipogenesis inhibition. However, Grail overexpression induced the same effects. Grail was shown to interact with PPARγ, targeting it for degradation and modulating its adipogenic activity. PPARγ expression was shown to be considerably reduced in Grail knockout (KO) mice fed normal diet or high-fat diet (HFD). The administration of both normal diet or HFD to Grail KO mice led to lower adipose mass and body weight than those in the wild-type mice. HFD-fed Grail KO mice had improved glucose and insulin tolerance. Taken together, our results indicate that Grail plays a pivotal role in adipogenesis and diet-induced obesity by regulating PPARγ activity.
Grail 是各种生物过程的关键调节剂,包括 T 细胞失能、抗病毒先天免疫反应和癌症的发生。然而,Grail 在脂肪生成和肥胖中的作用尚不清楚。在这里,我们证明了体外敲低 Grail 会导致 PPARγ 表达减少,从而抑制脂肪生成。然而,过表达 Grail 会产生相同的效果。Grail 被证明与 PPARγ 相互作用,将其靶向降解并调节其脂肪生成活性。在正常饮食或高脂肪饮食喂养的 Grail 敲除 (KO) 小鼠中,PPARγ 的表达明显减少。给予正常饮食或 HFD 喂养的 Grail KO 小鼠的脂肪量和体重均低于野生型小鼠。HFD 喂养的 Grail KO 小鼠的葡萄糖和胰岛素耐量得到改善。综上所述,我们的研究结果表明,Grail 通过调节 PPARγ 活性在脂肪生成和饮食诱导的肥胖中发挥关键作用。