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中文摘要
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描述(由申请方提供):该提案侧重于胆道系统的形态发生,胆道系统是将胆汁从肝细胞转运至肠道的管道。沿着沿着其复杂分支结构的任何点的胆管功能障碍都可能是发病率和死亡率的来源,并且重建正常的胆管完整性对于从损伤中恢复是必不可少的。本提案中描述的实验将深入了解如何沿着整个胆管树建立沿着连接,描绘Notch -一种其缺陷导致人类胆管缺陷的途径-调节肝脏发育的机制,并确定该途径在成人胆管功能中的作用。这项研究的长期目标是了解肝脏如何实现和维持其三维结构。拟议的实验将采用Cre/lox技术和实时成像检查几个参数的胆管形态发生在体内:形成的肝外肝内胆管连接,形成的导管小管连接,并建立胆管细胞极性和小管形成。该提案的一个中心目标是测试Notch信号通过启动细胞“tubulogenesis程序”控制胆管发育的假设,并测试该过程的特定候选介质在体外tubulogenesis中的作用。此外,还将进行研究以检查Notch信号如何与其他已知的胆管发育调节因子(例如HNF 1b,HNF 6,TGFb)协调。最后,实验提出,将测试的假设,Notch信号继续发挥作用,在整个生命的肝脏生物学,保持导管细胞的完整性和空间组织的响应损伤。公共卫生相关性:目前,终末期肝衰竭患者唯一有效的治疗方法是移植。替代方法开发的一个主要挑战是无法重现正常的肝细胞组织(形态发生)和体外功能。本研究的最终目标是描述指导肝脏正常分化和形态发生的事件,从而设计合理的肝脏再生和替代方法。
英文摘要
DESCRIPTION (provided by applicant): This proposal is focused on morphogenesis of the biliary system, the conduit for transport of bile from hepatocytes to the intestine. Dysfunction of the bile ducts at any point along its intricate branched structure can be a source of morbidity and mortality, and re-establishment of normal biliary integrity is essential for recovery from injury. The experiments described in this proposal will provide insight into how connectivity is established along the entirety of the biliary tree, delineate the mechanisms by which Notch - a pathway whose deficiency causes bile duct deficiency in humans - regulates liver development, and determine the role of this pathway in the function of adult bile ducts. The long-term objective of this research is to understand how the liver achieves and maintains its three dimensional architecture. The proposed experiments will employ Cre/lox technology and real-time imaging to examine several parameters of biliary morphogenesis in vivo: formation of the extrahepatic-intrahepatic biliary junction, formation of the ductal-canalicular junction, and the establishment of biliary cell polarity and tubule formation. A central goal of the proposal is to test the hypothesis that Notch signaling controls bile duct development by initiating a cellular "tubulogenesis program," and specific candidate mediators of this process will be tested for their role in tubulogenesis in vitro. In addition, studies will be performed to examine how Notch signals are coordinated with other known regulators of bile duct development (e.g. HNF1b, HNF6, TGFb). Finally, experiments are proposed that will test the hypothesis that Notch signaling continues to exert an effect on liver biology throughout life, by maintaining ductal cell integrity and spatially organizing the response to injury. PUBLIC HEALTH RELEVANCE: At present, the only effective treatment for patients with end-stage liver failure is transplantation. A major challenge to the development of alternative approaches is the inability to recapitulate normal liver cell organization (morphogenesis) and function outside of the body. The ultimate goal of this research is to delineate the events that guide differentiation and morphogenesis of the liver normally, and thereby devise rational approaches to liver regeneration and replacement.
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Molecular Determinants and Therapeutic Consequences of Immune Heterogeneity in Cancer
  • 批准号:
    10224134
  • 项目类别:
  • 资助金额:
    $65.73万
  • 财政年份:
    2018
  • 负责人:
    BEN Z STANGER
  • 依托单位:
Molecular Determinants and Therapeutic Consequences of Immune Heterogeneity in Cancer
  • 批准号:
    9754025
  • 项目类别:
  • 资助金额:
    $64.05万
  • 财政年份:
    2018
  • 负责人:
    BEN Z STANGER
  • 依托单位:
Molecular Determinants and Therapeutic Consequences of Immune Heterogeneity in Cancer
  • 批准号:
    10001329
  • 项目类别:
  • 资助金额:
    $82.01万
  • 财政年份:
    2018
  • 负责人:
    BEN Z STANGER
  • 依托单位:
Molecular Determinants and Therapeutic Consequences of Immune Heterogeneity in Cancer
  • 批准号:
    10532055
  • 项目类别:
  • 资助金额:
    $10.35万
  • 财政年份:
    2018
  • 负责人:
    BEN Z STANGER
  • 依托单位:
海外基金