Mechanisms of skeletal muscle repair and satellite cell regulation

骨骼肌修复和卫星细胞调节机制

基本信息

  • 批准号:
    RGPIN-2016-05747
  • 负责人:
  • 金额:
    $ 1.82万
  • 依托单位:
  • 依托单位国家:
    加拿大
  • 项目类别:
    Discovery Grants Program - Individual
  • 财政年份:
    2022
  • 资助国家:
    加拿大
  • 起止时间:
    2022-01-01 至 2023-12-31
  • 项目状态:
    已结题

项目摘要

Skeletal muscle displays incredible complexity and is comprised of many diverse cell types including muscle fibers, vasculature, stroma and neural cells. This cellular multiplicity endows muscle tissue with significant plasticity and the ability to remodel these cellular constituents in response to varied forms of muscle contraction. Additionally, skeletal muscle is one of the few adult organs with the remarkable ability to regenerate de novo tissue following trauma or strenuous muscle contraction. As muscle fibers are terminally differentiated (and not capable of cell division), this process is accomplished, at least in part, by the activity of muscle resident stem cells termed “satellite cells” (SCs). SCs respond to contraction or myotrauma by enhancing their activity through cell proliferation and ultimately fuse with existing muscle fibres to supply nuclei capable of synthesizing or repairing damaged muscle proteins. However, our understanding of the factors that influence SCs and their relationship to muscle physiology is incomplete, especially in human muscle.My research program strives to gain an understanding of the fundamental mechanisms that underpin SC function to lend insight into skeletal muscle homeostasis, and tissue remodeling. Since SCs are largely influenced by the environment in which they reside (known as the SC “niche”) a major goal of this research is to dissect the complexities of this specialized compartment. It is now appreciated that muscle contraction can alter the composition of the SC niche by stimulating the secretion of growth factor (GF) ligands that trigger the activation of SCs. Our work will utilize novel proteomic methods to uncover the function of new GFs and unidentified signaling receptors expressed by SC. Due to the complexity of skeletal muscle, we plan to take a systems biology approach with a focus on understanding the contribution of the non-myocellular components (e.g. stromal cells, vasculature, nervous system) of skeletal muscle in SC regulation. Utilizing the skeletal muscle microenvironment as a model system, we aim to gain a greater understanding of the cell intrinsic (autocrine) and cell-to-cell (paracrine) communication between SCs, muscle fibres and niche cells. Moreover, since contraction of muscle fibers induces acute perturbations to this muscle microenvironment while altering SC activity, our research will probe the synergies that underpin these events.Collectively, the information generated from this research program has the potential to impact our fundamental understanding of human SC regulation, muscle remodeling and skeletal muscle physiology. By utilizing many cutting-edge techniques and approaching questions from physiological, mechanistic, and systems biology angles our results will be relevant to a wide audience and will provide excellent training opportunities for highly qualified personnel.
骨骼肌表现出令人难以置信的复杂性,由许多不同的细胞类型组成,包括肌纤维、脉管系统、基质和神经细胞,这种细胞多样性赋予肌肉组织显着的可塑性以及重塑这些细胞成分以响应不同形式的肌肉收缩的能力。此外,骨骼肌是少数具有在创伤或剧烈肌肉收缩后从头再生组织的能力的成人器官之一,因为肌纤维是终末分化的(并且不能进行细胞分裂),这一过程至少部分是通过称为“卫星细胞”(SC) 的肌肉驻留干细胞的活性来完成的,SC 通过细胞增殖增强其活性并最终与现有的肌肉纤维融合以提供细胞核,从而对收缩或肌外伤作出反应。然而,我们对影响 SC 的因素及其与肌肉生理学的关系的了解并不完整,尤其是在人类肌肉中。我的研究项目致力于了解支持 SC 功能的基本机制。借由于 SC 在很大程度上受到其所处环境(称为 SC“利基”)的影响,因此这项研究的主要目标是剖析这种特殊隔室的复杂性。认识到肌肉收缩可以通过刺激生长因子 (GF) 配体的分泌来改变 SC 生态位的组成,从而触发 SC 的激活,我们的工作将利用新的蛋白质组学方法来揭示新 GF 的功能和未识别的信号传导。由于骨骼肌的复杂性,我们计划采用系统生物学方法,重点了解骨骼肌的非肌细胞成分(例如基质细胞、脉管系统、神经系统)在 SC 调节中的贡献。利用骨骼肌微环境作为模型系统,我们的目标是更好地了解 SC、肌肉之间的细胞内在(自分泌)和细胞间(旁分泌)通讯。此外,由于肌纤维的收缩会引起肌肉微环境的剧烈扰动,同时改变 SC 活动,因此我们的研究将探讨支撑这些事件的协同作用。总的来说,该研究项目产生的信息有可能影响我们的研究。对人类 SC 调节、肌肉重塑和骨骼肌生理学的基本了解通过利用许多尖端技术并从生理、机械和系统生物学角度解决问题,我们的结果将与广大受众相关,并将提供出色的培训。高素质人才的机会。

项目成果

期刊论文数量(0)
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Johnston, Adam其他文献

Combinatorial genetic analysis of a network of actin disassembly-promoting factors.
  • DOI:
    10.1002/cm.21231
  • 发表时间:
    2015-07
  • 期刊:
  • 影响因子:
    2.9
  • 作者:
    Ydenberg, Casey A.;Johnston, Adam;Weinstein, Jaclyn;Bellavance, Danielle;Jansen, Silvia;Goode, Bruce L.
  • 通讯作者:
    Goode, Bruce L.

Johnston, Adam的其他文献

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{{ truncateString('Johnston, Adam', 18)}}的其他基金

Mechanisms of skeletal muscle repair and satellite cell regulation
骨骼肌修复和卫星细胞调节机制
  • 批准号:
    RGPIN-2016-05747
  • 财政年份:
    2021
  • 资助金额:
    $ 1.82万
  • 项目类别:
    Discovery Grants Program - Individual
Mechanisms of skeletal muscle repair and satellite cell regulation
骨骼肌修复和卫星细胞调节机制
  • 批准号:
    RGPIN-2016-05747
  • 财政年份:
    2020
  • 资助金额:
    $ 1.82万
  • 项目类别:
    Discovery Grants Program - Individual
Mechanisms of skeletal muscle repair and satellite cell regulation
骨骼肌修复和卫星细胞调节机制
  • 批准号:
    RGPIN-2016-05747
  • 财政年份:
    2019
  • 资助金额:
    $ 1.82万
  • 项目类别:
    Discovery Grants Program - Individual
Mechanisms of skeletal muscle repair and satellite cell regulation
骨骼肌修复和卫星细胞调节机制
  • 批准号:
    RGPIN-2016-05747
  • 财政年份:
    2018
  • 资助金额:
    $ 1.82万
  • 项目类别:
    Discovery Grants Program - Individual
Mechanisms of skeletal muscle repair and satellite cell regulation
骨骼肌修复和卫星细胞调节机制
  • 批准号:
    RGPIN-2016-05747
  • 财政年份:
    2017
  • 资助金额:
    $ 1.82万
  • 项目类别:
    Discovery Grants Program - Individual
Mechanisms of skeletal muscle repair and satellite cell regulation
骨骼肌修复和卫星细胞调节机制
  • 批准号:
    RGPIN-2016-05747
  • 财政年份:
    2016
  • 资助金额:
    $ 1.82万
  • 项目类别:
    Discovery Grants Program - Individual
Satellite cell regulation by a local renin angiotensin system
局部肾素血管紧张素系统的卫星细胞调节
  • 批准号:
    363389-2008
  • 财政年份:
    2009
  • 资助金额:
    $ 1.82万
  • 项目类别:
    Postgraduate Scholarships - Doctoral
Satellite cell regulation by a local renin angiotensin system
局部肾素血管紧张素系统的卫星细胞调节
  • 批准号:
    363389-2008
  • 财政年份:
    2008
  • 资助金额:
    $ 1.82万
  • 项目类别:
    Postgraduate Scholarships - Doctoral

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    32301090
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    2023
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肌肉再生过程中骨骼肌干细胞内DNA G-四链体的功能和分子机制研究
  • 批准号:
    32300703
  • 批准年份:
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  • 资助金额:
    30 万元
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    青年科学基金项目
Gli1阳性肌肉干细胞在骨骼肌再生过程中的功能及机制研究
  • 批准号:
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  • 项目类别:
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探索乙二醛酶-1的调控机制
  • 批准号:
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  • 财政年份:
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  • 批准号:
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