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中文摘要
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描述(申请人提供):细胞间黏附是多细胞系统的基本特征。这项建议的目标是分析单个上皮细胞如何识别邻近细胞,以形成相互的细胞-细胞黏附,同时拒绝自我接触。两个相对细胞上的亲水性粘附性受体迅速结合,形成细胞间的粘附性,而来自同一细胞表面的两个薄突起上的相同受体则不会。这种对单个细胞的自我意识表明,细胞可以区分相邻细胞与自己细胞在化学上相同的表面。我们假设自我识别机制是机械调节的,钙粘附素复合体是一个检测外力的机械传感复合体,从而为相互细胞黏附提供信号提示。在没有外力的情况下,机械信号关闭,并导致自我接触的消除。使用创新的微制造基板来控制自接触事件,我们将分析自接触的形成和随后自接触点的消除。此外,我们还开发了微型力传感器来检测粘合剂接触处的力,并直接验证我们的假设。我们的发现还将强调相邻细胞之间如何形成相互的细胞-细胞黏附。一旦我们了解了细胞自我和其他识别的基本过程,我们的目标是开发能够改变细胞间黏附并可用于防止癌细胞入侵或病原体感染的治疗剂。 公共卫生相关性:细胞-细胞黏附的调节在多细胞生物体的发育和动态平衡中起着关键作用。这项提议的目标是分析单个上皮细胞如何识别邻近细胞,从而在拒绝自我接触的同时形成相互的细胞-细胞黏附。这项拟议研究的一个潜在结果将是开发先进的治疗药物,以防止癌细胞入侵或病原体感染。
英文摘要
DESCRIPTION (provided by applicant): Cell-cell adhesion is a fundamental feature of multi-cellular systems. The goal of this proposal is to analyze how individual epithelial cells recognize neighboring cells to form mutual cell-cell adhesion while rejecting self-contact. Homophilic adhesive receptors on two opposing cells rapidly bind to form a cell-cell adhesion, yet the same receptors on two thin protrusions originating from the same cell surface do not. This self-awareness of individual cells suggests that cells can distinguish the chemically identical surface of neighboring cells from their own. We hypothesize that the self-recognition mechanism is mechanically regulated, and that the cadherin complex is a mechano-sensing complex that detects external forces, thereby providing a signaling cue for mutual cell adhesion. In the absence of external forces, the mechano-signal is off, and leads to the elimination of self-contacts. Using innovative micro-fabricated substrates to control self-contacting events, we will analyze the formation of self-contacts and the subsequent elimination of self-contacting sites. Furthermore, we have developed miniature force sensors to detect forces at the adhesive contacts and directly test our hypothesis. Our findings will also highlight how mutual cell-cell adhesion forms between neighboring cells. Once we understand the fundamental processes of self and other recognition by cells, our goal is to develop therapeutic agents that alter cell- cell adhesion and can be used to prevent cancer cell invasion or pathogen infection. PUBLIC HEALTH RELEVANCE: Regulation of cell-cell adhesion plays critical roles in development and homeostasis of multi-cellular organisms. The goal of this proposal is to analyze how individual epithelial cells recognize neighboring cells to form mutual cell-cell adhesions while rejecting self-contact. One potential outcome of the proposed research will be the development of advanced therapeutic agents that prevent cancer cell invasion or pathogen infection.
期刊论文(13)
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会议论文
DOI: 10.1371/journal.pone.0122886
发表时间: 2015
期刊: PloS one
影响因子: 3.7
作者: [Ueda S, Blee AM, Macway KG, Renner DJ, Yamada S]
通讯作者: Yamada S
DOI: 10.4161/cam.21766
发表时间: 2012-11
期刊: Cell adhesion & migration
影响因子: 3.2
作者: [Shih W, Yamada S]
通讯作者: Yamada S
Live-cell imaging of migrating cells expressing fluorescently-tagged proteins in a three-dimensional matrix.
在三维矩阵中表达荧光标记蛋白的迁移细胞的活细胞成像。
DOI: 10.3791/3589
发表时间: 2011
期刊: Journal of visualized experiments : JoVE
影响因子: --
作者: [Shih,Wenting, Yamada,Soichiro]
通讯作者: Yamada,Soichiro
Self-contact elimination by membrane fusion.
通过膜融合消除自接触。
DOI: 10.1073/pnas.1311135110
发表时间: 2013
期刊: Proceedings of the National Academy of Sciences of the United States of America
影响因子: 11.1
作者: [Sumida,GrantM, Yamada,Soichiro]
通讯作者: Yamada,Soichiro
共 7 条
    Molecular basis of force-sensing by the keratin network
    • 批准号:
      10566716
    • 项目类别:
    • 资助金额:
      $44.71万
    • 财政年份:
      2023
    • 负责人:
      Soichiro Yamada
    • 依托单位:
    Identification of stretch-induced biotinylation at cadherin junctions
    Cell adhesion mediated self-recognition
    Cell adhesion mediated self-recognition
    海外基金