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染色质重塑蛋白BRG1通过激活肝细胞中SCAP的转录来调节SREBP成熟。

The Chromatin Remodeling Protein BRG1 Regulates SREBP Maturation by Activating SCAP Transcription in Hepatocytes.

作者信息

Kong Ming, Zhu Yuwen, Shao Jing, Fan Zhiwen, Xu Yong

机构信息

Key Laboratory of Targeted Intervention of Cardiovascular Disease and Collaborative Innovation Center for Cardiovascular Translational Medicine, Department of Pathophysiology, School of Basic Medical Sciences, Nanjing Medical University, Nanjing, China.

Wu Medical School, Jiangnan University, Wuxi, China.

出版信息

Front Cell Dev Biol. 2021 Feb 25;9:622866. doi: 10.3389/fcell.2021.622866. eCollection 2021.

Abstract

Sterol response element binding protein (SREBP) is a master regulator of cellular lipogenesis. One key step in the regulation of SREBP activity is its sequential cleavage and location by several different proteinases including SREBP cleavage activating protein (SCAP). We have previously reported that Brahma related gene 1 (BRG1) directly interacts with SREBP1c and SREBP2 to activate pro-lipogenic transcription in hepatocytes. We report here that BRG1 deficiency resulted in reduced processing and nuclear accumulation of SREBP in the murine livers in two different models of non-alcoholic steatohepatitis (NASH). Exposure of hepatocytes to lipopolysaccharide (LPS) and palmitate (PA) promoted SREBP accumulation in the nucleus whereas BRG1 knockdown or inhibition blocked SREBP maturation. Further analysis revealed that BRG1 played an essential role in the regulation of SCAP expression. Mechanistically, BRG1 interacted with Sp1 and directly bound to the SCAP promoter to activate SCAP transcription. Forced expression of exogenous SCAP partially rescued the deficiency in the expression of SREBP target genes in BRG1-null hepatocytes. In conclusion, our data uncover a novel mechanism by which BRG1 contributes to SREBP-dependent lipid metabolism.

摘要

固醇调节元件结合蛋白(SREBP)是细胞脂肪生成的主要调节因子。调节SREBP活性的一个关键步骤是其被包括SREBP裂解激活蛋白(SCAP)在内的几种不同蛋白酶进行顺序裂解和定位。我们之前报道过,与婆罗门相关基因1(BRG1)直接与SREBP1c和SREBP2相互作用,以激活肝细胞中的促脂肪生成转录。我们在此报告,在两种不同的非酒精性脂肪性肝炎(NASH)小鼠模型中,BRG1缺乏导致小鼠肝脏中SREBP的加工和核积累减少。将肝细胞暴露于脂多糖(LPS)和棕榈酸酯(PA)可促进SREBP在细胞核中的积累,而BRG1基因敲低或抑制则会阻断SREBP的成熟。进一步分析表明,BRG1在SCAP表达的调节中起重要作用。从机制上讲,BRG1与Sp1相互作用并直接结合到SCAP启动子上以激活SCAP转录。外源性SCAP的强制表达部分挽救了BRG1缺失肝细胞中SREBP靶基因表达的缺陷。总之,我们的数据揭示了一种新机制,通过该机制BRG1有助于SREBP依赖性脂质代谢。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4916/7947303/5f24414daf30/fcell-09-622866-g002.jpg

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