Role of aberrant regulation of organelle stress responses in alcohol-induced live

细胞器应激反应异常调节在酒精诱导的生活中的作用

• 批准号: 7932875
• 负责人: CHENG JI
• 金额: $ 38.09万
• 依托单位: UNIVERSITY OF SOUTHERN CALIFORNIA
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-09-15 至 2013-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7932875
• 关键词: Acetylation; Alcohol consumption; Alcoholic Liver Diseases; Alcohols; Animal Feed; Animal Model; Apoptosis; Biological Assay; CREB1 gene; Cell Death; Cessation of life; Chronic; Cirrhosis; Complex; DNA Polymerase II; Data; EP300 gene; Environmental Risk Factor; Epigenetic Process; Evolution; Fatty Liver; Fibrosis; Functional disorder; General Transcription Factors; Genes; Goals; Hepatic; Hepatocyte; In Situ Nick-End Labeling; Injury; Injury to Liver; Intracellular Accumulation of Lipids; Knockout Mice; Lead; Life; Link; Lipids; Liver; Liver diseases; Measures; Methylation; Mitochondria; Mus; Organelles; Oxidative Stress; Pathogenesis; Pathway interactions; Plasmids; Process; Regulation; Research; Research Personnel; Role; Serum; Staining method; Stains; Steatohepatitis; Stress; System; Testing; Tetanus Helper Peptide; Transgenic Mice; Transplantation; United States; Work; advanced system; biological adaptation to stress; calreticulin; cell injury; chronic alcohol ingestion; feeding; in vivo; injury and repair; knockout animal; mitochondrial dysfunction; novel strategies; oil red O; prevent; promoter; public health relevance; recombinase; response; transcription factor

DESCRIPTION (provided by applicant): The pathogenesis of alcohol-induced liver injury is very complex and undoubtedly involves the interplay of multiple mechanisms and pathways, dysfunction of cellular organelles, and interactions of intrinsic and environmental factors. The chronic feeding of alcohol leads to even more complexity as these processes of intracellular and intercellular injury and repair progress. We have focused our research on role of mitochondrial and ER stress responses in the evolution of alcohol-induced liver disease. We have obtained considerable data indicating that both mitochondria and ER are damaged by chronic alcohol consumption and that prolonged mitochondrial and ER stress responses contribute to liver injury including hepatic necroinflammation and cell death and severe fatty liver leading to fibrosis and cirrhosis. How alcohol regulates genetically and epigenetically the stress response genes of the two organelles is not known. To define the mechanisms by which alcohol consumption derails the mitochondrial and ER protective responses into injury promoting processes, we hypothesize that alcohol causes aberrant recruitment of transcription factors and epigenetic changes on the mitochondrial and ER stress response gene promoters which lead to liver injury. We propose to test the possibilities. The specific aims are: 1. Using quantitative PCR (qPCR) and ChIP assays, we will study the recruitment of promoter specific transcription factors (XBP-1, CHOP, ATF6, ATF4, CREB, TORC3, PGC-1a), general transcription factors (Pol II, NF-Y, NFR, Sp1, TBP and p300) and epigenetic marks (methylation of H3-K4 and H3-K79 and acetylation of H3 and H4) in promoters of mitochondrial and ER stress response genes (Grp78, Grp94, PDI, Calreticulin, HSP10, and HSP 60) by treating primary mouse hepatocytes with respective mitochondria and ER stress inducing agents; 2. We will perform in vivo study and measure the same parameters as described in Aim 1 with qPCR and ChIP assays by feeding mice alcohol compared to pair-fed control; 3. We will utilize Lox-Cre system as well as Dox-Tet advanced system to create and characterize liver specific Grp78 gene knockout mice; 4. We will determine effects of Grp78 deletion on the transcription factor recruitment and epigenetic changes on the two organelle gene promoters in the liver of mice fed alcohol, couple ER stress to mitochondrial dysfunction, and assess specific contribution of ER stress to alcohol-induced liver injury. Our overall goal is to reveal transcriptional and epigenetic abnormal regulation of the two organelle stress responses by alcohol in relation to the pathogenesis of alcoholic liver disease. We anticipate that this work will lead to new approaches to prevent or treat alcoholic liver disease and will be widely applicable in other types of liver disease. PUBLIC HEALTH RELEVANCE: Chronic excessive alcohol use leads to severe fatty liver and injury and is a leading cause of liver-related death and transplantation in the United States. We have identified links between liver disease and prolonged mitochondrial and ER stress responses caused by alcohol in animal models. This research is to understand how alcohol promotes injury processes in the two organelles and how organelle damages contribute to liver disease which will open new avenues for preventing and treating liver disease.

描述（申请人提供）：酒精性肝损伤的发病机制非常复杂，无疑涉及多种机制和途径的相互作用、细胞器功能障碍、内在因素和环境因素的相互作用。随着细胞内和细胞间损伤和修复过程的进展，慢性摄入酒精会导致更加复杂的过程。我们的研究重点是线粒体和内质网应激反应在酒精性肝病演变中的作用。我们获得的大量数据表明，线粒体和内质网都因慢性饮酒而受损，线粒体和内质网长期的应激反应会导致肝损伤，包括肝坏死、炎症和细胞死亡，以及导致纤维化和肝硬化的严重脂肪肝。酒精如何从遗传和表观遗传上调节这两种细胞器的应激反应基因尚不清楚。为了确定饮酒将线粒体和内质网保护反应详细描述为损伤促进过程的机制，我们假设酒精导致转录因子的异常募集和线粒体和内质网应激反应基因启动子的表观遗传变化，从而导致肝损伤。我们建议测试这些可能性。具体目标是：1。利用定量PCR （qPCR）和ChIP技术，我们将研究启动子特异性转录因子（XBP-1、CHOP、ATF6、ATF4、CREB、TORC3、PGC-1a）、一般转录因子（Pol II、NF-Y、NFR、Sp1、TBP和p300）和表观遗传标记（H3- k4和H3- k79甲基化和H3和H4乙酰化）在线粒体和内质网应激反应基因(Grp78、Grp94、PDI、Calreticulin、HSP10、和hsp60)分别用线粒体和内质网应激诱导剂处理原代小鼠肝细胞；2. 我们将进行体内研究，并通过qPCR和ChIP测定方法测量目标1中描述的相同参数，通过给小鼠喂食酒精与配对喂养对照组进行比较；3. 我们将利用Lox-Cre系统和Dox-Tet高级系统来创建和表征肝脏特异性Grp78基因敲除小鼠；4. 我们将确定Grp78缺失对酒精小鼠肝脏中转录因子募集和两种细胞器基因启动子表观遗传变化的影响，将内质网应激与线粒体功能障碍结合起来，并评估内质网应激对酒精诱导的肝损伤的具体贡献。我们的总体目标是揭示酒精对两种细胞器应激反应的转录和表观遗传异常调节与酒精性肝病的发病机制有关。我们预计这项工作将为预防或治疗酒精性肝病提供新的方法，并将广泛应用于其他类型的肝病。