PICOT and Cardiac Hypertrophy

PICOT 和心脏肥大

• 批准号: 7028769
• 负责人: Roger J. Hajjar
• 金额: $ 40.62万
• 依托单位: MASSACHUSETTS GENERAL HOSPITAL
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-02-01 至 2006-12-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7028769
• 关键词: binding proteins; binding sites; biological signal transduction; disease /disorder model; enzyme feedback; gene targeting; heart failure; kinase inhibitor; laboratory mouse; laboratory rat; protein isoforms; protein kinase C; transfection /expression vector; ventricular hypertrophy; yeast two hybrid system

DESCRIPTION (provided by applicant): Pressure overload-induced cardiac hypertrophy is one of the most common causes of heart failure. Many intracellular signal transduction pathways have been implicated in the development of cardiac hypertrophy and the progression of hypertrophy to heart failure, among which the protein kinase C (PKC) signaling pathway is the focus of this proposal. In preliminary studies, we found that 1) a PKC binding protein, PICOT (PKC-lnteracting Cousin Of Thioredoxin), is up-regulated during the development of cardiac hypertrophy and 2) enforced expression of PICOT in the neonatal rat ventricular myocyte (NRVM) and rat hearts abrogates the development of cardiac hypertrophy. These results suggest that PICOT is a key negative feedback regulator of cardiac hypertrophy, and thus provides a novel strategy to block the development of cardiac hypertrophy and heart failure. The goal of this proposal is to define the molecular mechanism of PKC inhibition by PICOT, and to evaluate the beneficial effects of PICOT overexpression in the rodent models of cardiac hypertrophy and heart failure. We propose the following specific aims: 1) Defining the molecular mechanism of PICOT activity and its interactions with other PKC isoforms, 2) Characterizing the PICOT complex by proteomic approaches, and 3) Defining the physiological consequences of PICOT overexpression in the hearts in vivo. Accomplishing these three specific aims will provide a greater understanding of the negative feedback mechanism of cardiac hypertrophy exerted by inhibiting PKC activity, and will allow for the design of novel therapeutic strategies for the management of cardiac hypertrophy and heart failure.

描述（由申请人提供）：压力超载引起的心脏肥厚是心力衰竭最常见的原因之一。许多细胞内信号转导通路涉及心脏肥厚的发生和肥厚向心力衰竭的进展，其中蛋白激酶C （PKC）信号通路是本研究的重点。在初步研究中，我们发现1)PKC结合蛋白PICOT （PKC- interinteracting Cousin Of Thioredoxin）在心肌肥厚的发展过程中被上调，2)新生大鼠心室肌细胞（NRVM）和大鼠心脏中PICOT的强制表达消除了心肌肥厚的发展。这些结果表明，PICOT是心脏肥厚的关键负反馈调节器，从而为阻止心脏肥厚和心力衰竭的发展提供了一种新的策略。本研究的目的是明确PICOT抑制PKC的分子机制，并评估PICOT过表达在心脏肥厚和心力衰竭啮齿动物模型中的有益作用。我们提出以下具体目标：1)确定PICOT活性的分子机制及其与其他PKC异构体的相互作用；2)通过蛋白质组学方法表征PICOT复合物；3)确定PICOT在体内心脏过表达的生理后果。实现这三个特定目标将有助于更好地理解通过抑制PKC活性产生的心脏肥厚的负反馈机制，并将允许设计新的治疗策略来管理心脏肥厚和心力衰竭。