Stretch-dependent X-ROS signaling: implications for cardiomyopathy

拉伸依赖性 X-ROS 信号传导：对心肌病的影响

• 批准号: 8354544
• 负责人: Benjamin Lears Prosser
• 金额: $ 13.47万
• 依托单位: UNIVERSITY OF MARYLAND BALTIMORE
• 依托单位国家: 美国
• 财政年份: 2012
• 资助国家: 美国
• 起止时间: 2012-08-20 至 2014-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8354544
• 关键词: Address; Adoption; Advisory Committees; Affect; Arrhythmia; Blood; Calcium; Calcium Signaling; Cardiac; Cardiology; Cardiomyopathies; Cell physiology; Cells; Clinical; Confocal Microscopy; Coupling; Development Plans; Diastole; Dilated Cardiomyopathy; Disease; Disease Progression; Disease model; Duchenne muscular dystrophy; Electrophysiology (science); Engineering; Enzymes; Equipment; Event; Faculty; Functional disorder; Generations; Goals; Growth; Heart; Heart Diseases; Heart failure; Homeostasis; Image; Knowledge; Lead; Length; Link; Maintenance; Maryland; Mentors; Mentorship; Modeling; Molecular; Mus; Muscle Cells; Myocardium; NADPH Oxidase; Oxidative Stress; Pathologic; Pathology; Phase; Phosphotransferases; Physiological; Physiology; Probability; Process; Production; Productivity; Reactive Oxygen Species; Regulation; Reporting; Research; Resources; Role; Ryanodine Receptors; Sarcoplasmic Reticulum; Science; Scientist; Signal Pathway; Signal Transduction; Source; Speed; Stretching; Surface; Techniques; Testing; Training; Training Support; Training Technics; Transgenic Mice; Translating; Universities; Ventricular; Work; base; calmodulin-dependent protein kinase II; career development; clinically relevant; defined contribution; experience; heart cell; heart rhythm; in vivo; inhibitor/antagonist; innovation; mdx mouse; medical schools; member; novel; novel therapeutics; patch clamp; pressure; professor; programs; research study; skills; small molecule

DESCRIPTION (provided by applicant): "Stretch-dependent X-ROS signaling: implications for cardiomyopathy" PI: Benjamin L. Prosser A novel signaling pathway in heart cells, termed X-ROS signaling, links the lengthening of a heart cell during diastole to the generation of reactive oxygen species (ROS) and subcellular Ca2+ signaling (Prosser et al., Science 2011). Discovered and characterized by the PI, X-ROS signaling regulates the release of Ca2+ from sarcoplasmic reticulum stores in heart cells. While X-ROS signaling is a normal physiological mechanism, it is upregulated in disease processes (e.g. Duchenne muscular dystrophy) and can trigger Ca2+-dependent arrhythmias. Using innovative techniques that combine the control of cell length with patch-clamp electrophysiology, the PI will characterize unknown critical biophysical features of this physiological generation of ROS, and investigate the signaling cascade that results. This biophysical characterization in single heart cells will be performed under the guidance of Dr. W.J. Lederer (mentor, University of Maryland), a world leader in cardiac cellular electrophysiology and calcium imaging. Through the adoption of new techniques and training, the PI will next move X-ROS signaling from the cellular level to that of the whole heart. The PI will image ROS and calcium signaling in intact, Langendorff-perfused hearts where diastolic length is modulated by a change in pre-load pressure. These examinations of length- dependent signaling will be conducted in both healthy and diseased hearts, as our recent evidence suggests that hyper-active X-ROS may be linked to calcium-dependent arrhythmia in disease. These studies will be guided by Dr. David Kass (co-mentor, Johns Hopkins School of Medicine), a translational cardiologist who specializes in the role of ROS signaling in cardiomyopathy. As a clinician scientist, Dr. Kass will broaden the perspective and skill set of the PI, which will allo the PI to take a more integrative approach to his work. The PI has assembled an excellent research advisory committee who will provide the training and support to facilitate the proposed studies and the growth of the PI. The PI will remain based at Maryland, but will work under the guidance of both Drs. Lederer and Kass during the entire period of work. Additionally, the PI has access to state-of-the-art equipment, as well as excellent resources for career development at the University of Maryland and at Johns Hopkins. The proposed work and development plan will enable the PI to characterize the physiological and pathophysiological actions of X-ROS signaling from the subcellular to the whole heart level, and will thus enable him to carve his niche as an independent faculty member. The proposed program is part of the PI's long term goal to investigate molecular mechanisms of cardiac function, with a particular focus on ROS and Ca2+ signaling, and to apply this knowledge to clinically relevant conditions.

描述（由申请人提供）：“Stretch-dependent X-ROS signaling：implications for cardiomyopathy”PI：Benjamin L. Prosser心脏细胞中的一种新的信号传导途径，称为X-ROS信号传导，将心肌细胞在心肌细胞中的延长与活性氧（ROS）和亚细胞Ca 2+信号传导的产生联系起来（Prosser等人，Science 2011）。由PI发现并表征的X-ROS信号调节心肌细胞中肌浆网储存的Ca 2+释放。虽然X-ROS信号传导是一种正常的生理机制，但它在疾病过程（例如杜氏肌营养不良症）中上调，并可触发Ca 2+依赖性心律失常。使用创新的技术，结合联合收割机的细胞长度与膜片钳电生理学的控制，PI将表征未知的关键生物物理特征的生理产生的ROS，并调查信号级联的结果。将在心脏细胞电生理学和钙成像领域的世界领先者W. J. Lederer博士（导师，马里兰州大学）的指导下，在单个心脏细胞中进行该生物物理表征。通过采用新技术和培训，PI下一步将把X-ROS信号从细胞水平转移到整个心脏的水平。PI将在完整的Langendorff灌注心脏中对ROS和钙信号进行成像，其中舒张长度由前负荷压力的变化调节。这些长度依赖性信号传导的检查将在健康和患病的心脏中进行，因为我们最近的证据表明，过度活跃的X-ROS可能与疾病中的钙依赖性心律失常有关。这些研究将由大卫卡斯博士（共同导师，约翰霍普金斯医学院）指导，他是一位翻译心脏病学家，专门研究ROS信号在心肌病中的作用。作为一名临床科学家，Kass博士将拓宽PI的视角和技能，这将使PI在工作中采取更加综合的方法。PI已经组建了一个优秀的研究咨询委员会，该委员会将提供培训和支持，以促进拟议的研究和PI的发展。主要研究者将留在马里兰州，但在整个工作期间将在Lederer博士和Kass博士的指导下工作。此外，PI还可以使用最先进的设备，以及马里兰州大学和约翰霍普金斯大学的职业发展资源。拟议的工作和发展计划将使PI能够表征从亚细胞到整个心脏水平的X-ROS信号传导的生理和病理生理作用，从而使他能够作为一名独立的教员开拓自己的利基。该计划是PI长期目标的一部分，旨在研究心脏功能的分子机制，特别关注ROS和Ca 2+信号传导，并将这些知识应用于临床相关疾病。