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Self-Organogenesis from 2D Micropatterns to 3D Biomimetic Biliary Trees

机译:从 2D 微模式到 3D 仿生胆树的自器官发生

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摘要

Background and Aims: Globally, liver diseases account for 2 million deaths per year. For those with advanced liver disease the only curative approach is liver transplantation. However, less than 10% of those in need get a liver transplant due to limited organ availability. To circumvent this challenge, there has been a great focus in generating a bioengineered liver. Despite its essential role in liver functions, a functional biliary system has not yet been developed. In this framework, exploration of epithelial cell self-organogenesis and microengineering-driven geometrical cell confinement allow to envision the bioengineering of a functional biomimetic intrahepatic biliary tract. Approach: three-dimensional (3D) bile ducts were built in vitro by restricting cell adhesion to two-dimensional (2D) patterns to guide cell self-organization. Tree shapes mimicking the configuration of the human biliary system were micropatterned on glass slides, restricting cell attachment to these areas. Different tree geometries and culture conditions were explored to stimulate self-organogenesis of normal rat cholangiocytes (NRCs) used as a biliary cell model, either alone or in co-culture with human umbilical endothelial cells (HUVECs). Results: Pre-seeding the micropatterns with HUVECs promoted luminogenesis with higher efficiency to yield functional branched biliary tubes. Lumen formation, apico-basal polarity, and preservation of the cholangiocyte phenotype were confirmed. Moreover, intact and functional biliary structures were detached from the micropatterns for further manipulation. Conclusion: This study presents physiologically relevant 3D biliary duct networks built in vitro from 2D micropatterns. This opens opportunities for investigating bile duct organogenesis, physiopathology, and drug testing.
机译:背景和目标: 在全球范围内,肝病每年导致 200 万人死亡。对于晚期肝病患者,唯一的治疗方法是肝移植。然而,由于器官可用性有限,只有不到 10% 的有需要的人接受了肝移植。为了规避这一挑战,人们一直非常重视生成生物工程肝脏。尽管它在肝功能中起着重要作用,但功能性胆道系统尚未开发出来。在这个框架中,对上皮细胞自身器官发生的探索和微工程驱动的几何细胞限制允许设想功能性仿生肝内胆道的生物工程。方法:通过将细胞粘附限制为二维 (2D) 模式来指导细胞自组织,在体外构建三维 (3D) 胆管。模拟人类胆道系统配置的树形在载玻片上被微图案化,限制细胞附着在这些区域。探索了不同的树木几何形状和培养条件,以刺激用作胆汁细胞模型的正常大鼠胆管细胞 (NRC) 的自身器官发生,无论是单独使用还是与人脐带内皮细胞 (HUVEC) 共培养。结果: 用 HUVECs 预接种微模式以更高的效率促进发光,从而产生功能性分支胆管。证实了管腔形成、顶端-基底极性和胆管细胞表型的保留。此外,完整和功能性的胆道结构从微模式中分离出来,以便进一步操作。结论: 本研究提出了从 2D 微模式体外构建的生理相关的 3D 胆管网络。这为研究胆管器官发生、生理病理学和药物检测提供了机会。

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