Mechanisms of Bile Duct Morphogenesis

胆管形态发生的机制

• 批准号: 8274748
• 负责人: BEN Z STANGER
• 金额: $ 33.44万
• 依托单位: UNIVERSITY OF PENNSYLVANIA
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-07-01 至 2014-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8274748
• 关键词: Address; Adult; Architecture; Bile fluid; Biliary; Biology; Cell Polarity; Cell Survival; Cell Therapy; Cells; Communication; Congenital Abnormality; Development; Drug Metabolic Detoxication; Ductal; Ductal Epithelial Cell; Embryo; Embryonic Development; Epithelial Cells; Event; Experimental Models; Extrahepatic; Extrahepatic Bile Ducts; Fibrosis; Functional disorder; Goals; Hepatobiliary; Hepatocyte; Human; Image; In Vitro; Injury; Intestines; Intrahepatic bile duct; Life; Liver; Liver Failure; Liver Regeneration; Liver diseases; Maintenance; Mediator of activation protein; Molecular; Morbidity - disease rate; Morphogenesis; Morphology; Mus; Natural regeneration; Normal tissue morphology; Obstruction; Organ; Pathway interactions; Patients; Play; Process; Recovery; Regulation; Research; Role; Signal Transduction; Source; Staging; Structure; Technology; Testing; Time; Transplantation; Trees; abstracting; bile duct; biliary tract; chronic liver disease; effective therapy; in vivo; insight; intrahepatic; liver function; mortality; notch protein; postnatal; programs; research study; response; response to injury; three dimensional structure

Abstract 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.

摘要 这项建议的重点是胆管系统的形态发生，胆管系统是一个管道， 胆汁从肝细胞到肠的转运。任何时候的胆管功能障碍 点沿着其复杂的分支结构可以是发病率和死亡率的来源， 并且重建正常的胆道完整性对于损伤的恢复是必要的。的 本提案中描述的实验将提供有关连通性如何 沿着整个胆道树建立，描述了 Notch --一种其缺陷导致人类胆管缺陷的途径--调节 肝脏发育，并确定这一途径在成人胆汁功能中的作用 管道 这项研究的长期目标是了解肝脏如何实现和 保持其三维结构。拟议的实验将采用 Cre/lox技术和实时成像检查胆道的多个参数 体内形态发生：肝外-肝内胆管连接的形成， 胆管-小管连接处的形成和胆管细胞极性的建立 和小管形成。该提案的一个中心目标是检验Notch 信号传导通过启动细胞的“管生成程序”来控制胆管发育， 这一进程的具体候选调解人将接受测试，以确定他们在以下方面的作用： 体外小管形成。此外，还将进行研究，以检查Notch 信号与胆管发育的其他已知调节因子（例如， HNF 1b、HNF 6、TGFb）。最后，实验提出，将测试的假设 Notch信号在整个生命过程中继续对肝脏生物学产生影响， 维持导管细胞的完整性并在空间上组织对损伤的反应。