Systems Approach to Understanding Cardiovascular Disease and Arrhythmias - Cell diversity in the cardiovascular system, cell-autonomous and cell-cell signaling

了解心血管疾病和心律失常的系统方法 - 心血管系统中的细胞多样性、细胞自主和细胞间信号传导

基本信息

  • 批准号:
    10386681
  • 负责人:
  • 金额:
    $ 3万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2021
  • 资助国家:
    美国
  • 起止时间:
    2021-11-23 至 2022-10-31
  • 项目状态:
    已结题

项目摘要

UC Davis Cardiovascular Symposium Systems Approach to Understanding Cardiovascular Disease and Arrhythmias -Cell diversity in the cardiovascular system, cell-autonomous and cell-cell signaling- Cardiovascular diseases, including hypertension, heart failure, arrhythmias and stroke, are the number one killer in the developed world. In order to develop better and more effective therapies to treat heart diseases, it is critically important for scientists and physicians to obtain in-depth and accurate understanding of the mechanisms underlying heart and vascular function and dysfunction. In recent decades, researchers studying heart and vascular diseases have been accumulating more and more experimental data from molecular, to cellular, and to tissue and organ levels. However, there is a critical need to integrate these data into mechanistic and quantitative models to understand emergent properties of complex biological system such as arrhythmias and vasospasms that are often counterintuitive (due to non-linear dynamics interactions). Moreover, it is important to understand how different cells of the cardiovascular system may interact with each other in physiology and disease. Here we propose to take the necessary step forward to integrate experimental data into quantitative models that enable using mathematical tools and computational power to understand the complex interactions of the cells and molecules in the cardiovascular system. The unique design of this conference series is to combine experimental study and mathematical modeling to achieve in-depth understanding of the dynamic systems that control cardiovascular function and diseases. The proposed interdisciplinary conference is the 7th in this series. This new installment of the conference will integrate, for the first time, studies in cardiac and vascular tissue. The previous conferences have received overwhelmingly positive evaluations from attendees and resulted in high impact publications. The proposed conference will combine experimental and modeling studies in the field of cardiac and vascular physiology, with topics focused on cell diversity in the cardiovascular system, as it is becoming increasingly evident that a complex interplay of abnormal signaling events among various cell types, including myocytes, fibroblasts, endothelial, neuronal, immune cells, etc. plays a central role in cardiovascular disease. The emphasis of this conference will be on (1) summarizing current state of research in the focus area, (2) identifying consensus and controversy that warrant more investigation, and (3) exchanging ideas, data, and information among the experimentalists and modelers to facilitate interdisciplinary collaborations. The conference results will be summarized in the form of comprehensive review papers, which will be published in leading scientific journals that have broad impact on the research community, as before.
加州大学戴维斯分校心血管研讨会 了解心血管疾病和心律失常的系统方法 - 心血管系统中的细胞多样性,细胞自主和细胞间信号传导- 包括高血压、心力衰竭、心律失常和中风在内的心血管疾病是头号杀手 in the developed发达world世界.为了开发更好更有效的治疗心脏病的方法, 对科学家和医生来说,深入和准确地了解 心脏和血管功能和功能障碍的潜在机制。近几十年来,研究人员 心脏和血管疾病已经积累了越来越多的实验数据,从分子, 细胞水平,以及组织和器官水平。然而,迫切需要将这些数据集成到机械化的 和定量模型,以了解复杂生物系统的涌现特性,如心律失常 以及通常违反直觉的血管痉挛(由于非线性动力学相互作用)。而且是 重要的是要了解心血管系统的不同细胞如何相互作用, 生理学和疾病。在这里,我们建议采取必要的步骤,将实验数据整合到 定量模型,使使用数学工具和计算能力,以了解复杂的 心血管系统中细胞和分子的相互作用。本次会议系列的独特设计 是将联合收割机的实验研究和数学建模相结合, 控制心血管功能和疾病的系统。本次跨学科会议是第七届 在这个系列中。会议的这一新的分期付款将首次整合心脏和心脏病的研究, 血管组织前几届会议得到了与会者压倒性的积极评价 并出版了影响深远的出版物。拟议的会议将结合联合收割机实验和建模 心脏和血管生理学领域的研究,主题集中在心血管系统中的细胞多样性 系统,因为越来越明显,异常信号事件之间的复杂相互作用 各种类型的细胞,包括肌细胞、成纤维细胞、内皮细胞、神经细胞、免疫细胞等,都起着核心作用 在心血管疾病中。本次会议的重点将是(1)总结研究现状 在重点领域,(2)确定需要更多调查的共识和争议,(3)交换 想法,数据和信息之间的实验和建模,以促进跨学科的合作。 会议成果将以综合评论论文的形式进行总结,并予以发表 在领先的科学期刊,有广泛的影响力的研究界,像以前一样。

项目成果

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Donald M Bers其他文献

The Difference of Calmodulin-Ryanodine Receptor Affinity Between N-terminal, Central and C-terminal RyR2-CPVT Knock-in Mice
N端、中央端和C端RyR2-CPVT敲入小鼠钙调蛋白-兰尼定受体亲和力的差异
  • DOI:
  • 发表时间:
    2019
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Hitoshi Uchinoumi;Xiaoqiong Dong;Ivanita Stefanon;Mena Said;Rogerio Faustino;Razvan L Cornea;Univ of Minnesota;Xander H.t. Wehrens; Takeshi Yamamoto;Masafumi Yano;Donald M Bers
  • 通讯作者:
    Donald M Bers
Beyond beta blockers
超越β受体阻滞剂
  • DOI:
    10.1038/nm0405-379
  • 发表时间:
    2005-04-01
  • 期刊:
  • 影响因子:
    50.000
  • 作者:
    Donald M Bers
  • 通讯作者:
    Donald M Bers

Donald M Bers的其他文献

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{{ truncateString('Donald M Bers', 18)}}的其他基金

Training Program in Pharmacology
药理学培训计划
  • 批准号:
    10656570
  • 财政年份:
    2022
  • 资助金额:
    $ 3万
  • 项目类别:
Project 2 (Bers)
项目2(Bers)
  • 批准号:
    10677715
  • 财政年份:
    2019
  • 资助金额:
    $ 3万
  • 项目类别:
Systems Approach to Understanding Cardiac Arrhythmias Mechanisms
了解心律失常机制的系统方法
  • 批准号:
    9763307
  • 财政年份:
    2019
  • 资助金额:
    $ 3万
  • 项目类别:
Project 2 (Bers)
项目2(Bers)
  • 批准号:
    10006341
  • 财政年份:
    2019
  • 资助金额:
    $ 3万
  • 项目类别:
Modelling structural and functional heterogeneity in heart failure reveals arrhythmic impact
心力衰竭的结构和功能异质性建模揭示了心律失常的影响
  • 批准号:
    10199780
  • 财政年份:
    2019
  • 资助金额:
    $ 3万
  • 项目类别:
Modelling structural and functional heterogeneity in heart failure reveals arrhythmic impact
心力衰竭的结构和功能异质性建模揭示了心律失常的影响
  • 批准号:
    10449125
  • 财政年份:
    2019
  • 资助金额:
    $ 3万
  • 项目类别:
Project 2 (Bers)
项目2(Bers)
  • 批准号:
    10249148
  • 财政年份:
    2019
  • 资助金额:
    $ 3万
  • 项目类别:
Project 2 (Bers)
项目2(Bers)
  • 批准号:
    10471339
  • 财政年份:
    2019
  • 资助金额:
    $ 3万
  • 项目类别:
CaMKII activation and regulation in adult cardiac myocytes
成人心肌细胞中 CaMKII 的激活和调节
  • 批准号:
    10687251
  • 财政年份:
    2018
  • 资助金额:
    $ 3万
  • 项目类别:
High-Throughput Screens to Discover Novel Inhibitors of Leaky RyR2 for Heart Failure Therapy
高通量筛选发现用于心力衰竭治疗的漏性 RyR2 新型抑制剂
  • 批准号:
    10064096
  • 财政年份:
    2018
  • 资助金额:
    $ 3万
  • 项目类别:

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开发人类干细胞衍生的心脏模型来表征新型心律失常综合征
  • 批准号:
    495592
  • 财政年份:
    2023
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Preliminary Study to Establish Heavy Ion Ablation Therapy for Lethal Ventricular Arrhythmia
重离子消融治疗致死性室性心律失常的初步研究
  • 批准号:
    23K14885
  • 财政年份:
    2023
  • 资助金额:
    $ 3万
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    Grant-in-Aid for Early-Career Scientists
Arrhythmia Mechanisms Modulated by Intercalated Disc Extracellular Nanodomains
闰盘细胞外纳米结构域调节心律失常的机制
  • 批准号:
    10668025
  • 财政年份:
    2023
  • 资助金额:
    $ 3万
  • 项目类别:
Development of a next-generation telemonitoring system for prognostic prediction of the onset of heart failure and arrhythmia
开发下一代远程监测系统,用于心力衰竭和心律失常发作的预后预测
  • 批准号:
    23K09597
  • 财政年份:
    2023
  • 资助金额:
    $ 3万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
The role of inflammation in the pathogenesis of atrial fibrillation: Implications for atrial remodeling pathophysiology and for early atrial arrhythmia recurrences following radiofrequency ablation and pulsed field ablation
炎症在心房颤动发病机制中的作用:对心房重塑病理生理学以及射频消融和脉冲场消融后早期房性心律失常复发的影响
  • 批准号:
    514892030
  • 财政年份:
    2023
  • 资助金额:
    $ 3万
  • 项目类别:
    WBP Fellowship
Improved arrhythmia ablation via MR-guided robotic catheterization and multimodal clinician feedback
通过 MR 引导的机器人导管插入术和多模式临床医生反馈改善心律失常消融
  • 批准号:
    10638497
  • 财政年份:
    2023
  • 资助金额:
    $ 3万
  • 项目类别:
Prototype development and validation of soft robotic sensor arrays for mapping cardiac arrhythmia
用于绘制心律失常的软机器人传感器阵列的原型开发和验证
  • 批准号:
    10722857
  • 财政年份:
    2023
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    $ 3万
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The role N-terminal acetylation in dilated cardiomyopathy and associated arrhythmia
N-末端乙酰化在扩张型心肌病和相关心律失常中的作用
  • 批准号:
    10733915
  • 财政年份:
    2023
  • 资助金额:
    $ 3万
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A novel regulator of Ca2+ homeostasis and arrhythmia susceptibility
Ca2 稳态和心律失常易感性的新型调节剂
  • 批准号:
    10724935
  • 财政年份:
    2023
  • 资助金额:
    $ 3万
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Novel Stellate Ganglia Chemo-ablation Approach to Treat Cardiac Arrhythmia and Cardiac Remodeling in Heart Failure
新型星状神经节化疗消融方法治疗心律失常和心力衰竭心脏重塑
  • 批准号:
    10727929
  • 财政年份:
    2023
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    $ 3万
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