Bai Danna, Zhang Yajun, Shen Mingzhi, Sun Yongfeng, Xia Qing, Zhang Yingmei, Liu Xuedong, Wang Haichang, Yuan Lijun
Department of Cardiology, Xijing Hospital, the Fourth Military Medical University, Xi'an 710032, China.
323 Hospital of PLA, Xi'an 710054, China.
Sci Rep. 2016 Feb 24;6:22068. doi: 10.1038/srep22068.
The leading cause of death in diabetic patients is diabetic cardiomyopathy, in which alteration of Akt signal plays an important role. Inpp5f is recently found to be a negative regulator of Akt signaling, while its expression and function in diabetic heart is largely unknown. In this study, we found that in both the streptozotocin (STZ) and high fat diet (HFD) induced diabetic mouse models, Inpp5f expression was coordinately regulated by insulin, blood glucose and lipid levels. Increased Inpp5f was inversely correlated with the cardiac function. Further studies revealed that Insulin transcriptionally activated Inpp5f in an Sp1 dependent manner, and increased Inpp5f in turn reduced the phosphorylation of Akt, forming a negative feedback loop. The negative feedback plays a protective role under diabetic condition. However, high blood glucose and lipid, which are characteristics of uncontrolled diabetes and type 2 diabetes, increased Inpp5f expression through activation of NF-κB, blunts the protective feedback. Thus, our study has revealed that Inpp5f provides as a negative feedback regulator of insulin signaling and downregulation of Inpp5f in diabetes is cardioprotective. Increased Inpp5f by hyperglycemia and hyperlipidemia is an important mediator of diabetic cardiomyopathy and is a promising therapeutic target for the disease.
糖尿病患者的主要死因是糖尿病性心肌病,其中Akt信号的改变起着重要作用。最近发现Inpp5f是Akt信号的负调节因子,但其在糖尿病心脏中的表达和功能尚不清楚。在本研究中,我们发现,在链脲佐菌素(STZ)和高脂饮食(HFD)诱导的糖尿病小鼠模型中,Inpp5f的表达受胰岛素、血糖和血脂水平的协同调节。Inpp5f的增加与心脏功能呈负相关。进一步研究表明,胰岛素以依赖Sp1的方式转录激活Inpp5f,而Inpp5f的增加反过来降低Akt的磷酸化,形成负反馈环。这种负反馈在糖尿病状态下起保护作用。然而,不受控制的糖尿病和2型糖尿病的特征性高血糖和高血脂通过激活NF-κB增加Inpp5f的表达,削弱了这种保护反馈。因此,我们的研究表明,Inpp5f作为胰岛素信号的负反馈调节因子,糖尿病中Inpp5f的下调具有心脏保护作用。高血糖和高血脂导致的Inpp5f增加是糖尿病性心肌病的重要介质,是该疾病有前景的治疗靶点。