Wang Min, Zhao Shuiping, Tan Mingyue
Department of Cardiology, The Second Xiangya Hospital, Central South University, Changsha, Hunan 410000, P.R. China.
Mol Med Rep. 2016 Feb;13(2):1455-62. doi: 10.3892/mmr.2015.4749. Epub 2015 Dec 30.
The cyclic adenosine monophosphate (cAMP)-responsive element-binding protein H (CREBH) is a transcription factor localized to the endoplasmic reticulum (ER) membrane. Previous studies have demonstrated that CREBH is activated by ER stress, hepatic glucose and lipid metabolism signaling, and inflammation. Thus, it may be critical in the regulation of various physiological functions associated with the development of non-alcoholic fatty liver disease (NAFLD), which results from inflammation and disorder of hepatic glucose and lipid metabolism. Therefore, CREBH may have potential as a pharmacological target for NAFLD. This review summarizes recent scientific developments and the biological actions of CREBH with a particular focus on its involvement in NAFLD.
环磷酸腺苷(cAMP)反应元件结合蛋白H(CREBH)是一种定位于内质网(ER)膜的转录因子。先前的研究表明,CREBH可被内质网应激、肝脏葡萄糖和脂质代谢信号以及炎症激活。因此,它可能在调节与非酒精性脂肪性肝病(NAFLD)发展相关的各种生理功能中起关键作用,NAFLD是由肝脏葡萄糖和脂质代谢的炎症和紊乱引起的。因此,CREBH可能具有作为NAFLD药物靶点的潜力。本综述总结了CREBH的最新科学进展及其生物学作用,特别关注其在NAFLD中的作用。