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Molecular mechanisms regulating cell fate

Molecular mechanisms regulating cell fate
调控细胞命运的分子机制
批准号:
402152-2011
负责人:
Christian, Sherri
金额:
$2.55万
依托单位国家:
加拿大
项目类别:
Discovery Grants Program - Individual
财政年份:
2014
资助国家:
加拿大
项目状态:
已结题
起止时间:
2014-01-01 至 2015-12-31

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中文摘要
翻译
细胞通过细胞表面的蛋白质与环境相互作用,这种蛋白质称为受体。通过多米诺骨牌效应,这些受体的激活导致细胞内一系列蛋白质的激活。这一系列蛋白质被称为信号通路。然后,这些通路指示细胞如何对环境做出反应。通过激活这些途径,细胞可以被指示分裂、发育或死亡,以及其他后果。有时,根据细胞类型或其他环境信号的不同,同一通路的激活可能会导致截然不同的后果。目前尚不清楚激活相同的途径如何会对细胞或细胞命运产生不同的后果。基督教实验室感兴趣的是,即使在共同的蛋白质、受体或通路被激活的情况下,指导不同细胞命运的机制也是如此。在开始这项工作之前,我们将重点放在一个模型系统上,在这个系统中,一种被称为CD24的受体根据细胞类型的不同而产生非常不同的影响。如果CD24被激活,注定要成为抗体产生细胞的细胞,即B细胞,将会死亡。相反,在一些癌细胞中,CD24指示细胞存活。我们的目标是确定决定特定细胞对CD24的反应是存活还是死亡的机制。这些研究将极大地提高我们对细胞如何决定其生存或死亡的理解。此外,对这些机制的表征可能会识别出可能以改变细胞生存或死亡能力为目标的蛋白质。
英文摘要
Cells interact with their environment through proteins at the cell surface, known as receptors. Through a domino effect, the activation of these receptors causes activation of a series of proteins inside in the cell. This series of proteins is known as a signalling pathway. These pathways then instruct the cell how to respond to its environment. By activating these pathways, a cell can be instructed to, among other consequences, divide, develop, or die. Sometimes activation of the same pathway can result in drastically different consequences depending on the cell type or other environmental signals. It is not clear how activation of the same pathway can result in different consequences for the cell, or cell fates. The Christian lab is interested in understanding the mechanisms that direct different cell fates even when common proteins, receptors or pathways are activated. To begin this work, we will focus on a model system where one receptor, known as CD24, causes very different effects depending on the cell type. Cells that are destined to become antibody-producing cells, known as B cells, will die if CD24 is activated. In contrast, in some cancer cells CD24 instructs the cell to survive. Our goal is to identify the mechanisms that determine if a specific cell will live or die in response to CD24. These studies will significantly improve our understanding of how cells decide if they will live or die. Furthermore, the characterization of these mechanisms may identify proteins that could be targeted to alter the ability of a cell to live or die.
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Role and regulation of extracellular vesicles generated in response to stimulation of CD24 on B lymphocytes
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    RGPIN-2022-03800
  • 项目类别:
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  • 财政年份:
    2022
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Characterization of extracellular microvesicles generated by immature B cell as mediators of cell-cell communication
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  • 项目类别:
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    $1.89万
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Characterization of extracellular microvesicles generated by immature B cell as mediators of cell-cell communication
  • 批准号:
    RGPIN-2017-04630
  • 项目类别:
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  • 资助金额:
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  • 财政年份:
    2020
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  • 依托单位:
Characterization of extracellular microvesicles generated by immature B cell as mediators of cell-cell communication
  • 批准号:
    RGPIN-2017-04630
  • 项目类别:
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  • 资助金额:
    $1.89万
  • 财政年份:
    2019
  • 负责人:
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Exploring the Intrinsic Mechanisms of CEO Turnover and Market Reaction: An Explanation Based on Information Asymmetry
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  • 项目类别:
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  • 项目类别:
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