Micropatterned scaffold-free liver tissue

微图案无支架肝组织

• 批准号: 8058999
• 负责人: Kelly R Stevens
• 金额: $ 5.13万
• 依托单位: MASSACHUSETTS INSTITUTE OF TECHNOLOGY
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-02-05 至 2014-02-04
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8058999
• 关键词: Architecture; Artificial Organs; Biocompatible Materials; Biology; Blood Vessels; Cardiac; Cells; Centrifugation; Clinical; Communities; Development; Disease model; Endothelial Cells; Engineering; Engraftment; Exhibits; Extracellular Matrix; Face; Fibroblasts; Future; Hepatocyte; Human; Immune response; In Vitro; Indium; Knowledge; Label; Liver; Mesenchymal; Methods; Microscopy; Modeling; Molds; Morphogenesis; Movement; Nature; Necrosis; Organ; Organ Transplantation; Organ failure; Patients; Pattern; Pharmacologic Substance; Poison; Polymers; Population; Process; Research; Role; Signal Transduction; Stromal Cells; Structure; System; Techniques; Technology; Testing; Time; Tissue Engineering; Tissues; Transplantation; Work; angiogenesis; base; bile canaliculus structure; cell type; density; design; drug development; human tissue; in vivo; novel; novel strategies; scaffold; systems research; time use; tool

DESCRIPTION (provided by applicant): Severe lack of functional human tissue and organ-substitutes precludes clinical transplantation for most patients suffering from organ failure. Additionally, robust human models are needed for research and pharmaceutical development. Engineered artificial organs and tissues could provide alternatives or bridges to organ transplant and in vitro systems for drug development or disease modeling. "Classical" biomaterial- and extracellular matrix-based tissue engineering faces several challenges, such as the unfavorable host response to biomaterials, toxic substances released by scaffold degradation products, and low cellular density. Scaffold- free tissue engineering seeks to create dense 3D tissues only from cells and the matrix they secrete (without the use of polymers and exogenous matrix). To date, such multi-cellular scaffold-free "tissues" have been created by random mixing of multiple cell types, and any organization has been the result of cellular self- organization1-5. These systems frequently exhibit highly variable cellular morphogenesis (e.g., variable endothelial cell network formation) as well as necrosis at the tissue core. Controlled assembly has been largely unexplored in scaffold-free systems. Indeed, a central unanswered question in tissue engineering is the degree to which engineers will need to control absolute architecture versus "coax" biology to self-organize into tissues via morphogenesis. We hypothesize that pre-determined spatial organization of cells within engineered tissues will facilitate cellular organization and maximize tissue function, which we define as "guided morphogenesis". In this proposal, we will study how spatial signals drive emergent morphogenesis and tissue organization between communities of cells by spatially controlling the initial architecture of engineered scaffold-free multi-cellular tissues. We will develop a platform to micropattern 3D multi-cellular scaffold-free tissues and then study how pre-defined tissue architecture dictates both tissue function and vascular morphogenesis. We will specifically apply these methods to study how modulation of 3D multi-cellular tissue architecture impacts differentiated hepatocyte function and organization as well as microvascular morphogenesis in engineered scaffold-free liver tissue. The ultimate objective of this work is to develop platforms that enable the study of spatially-controlled multicellular interactions in 3D tissue development and function in order to establish architectural "design specifications" for engineering liver tissue. We expect that such technologies will greatly facilitate the design of future cell-based technologies and engineered tissues. ) PUBLIC HEALTH RELEVANCE: Artificially engineered tissues (e.g., liver) could serve as organ-substitutes for clinical transplantation as well as test systems for research and pharmaceutical development. Here, we will develop novel engineering tools to study how nature organizes different types of "cellular building blocks" in building three-dimensional tissues. This knowledge could be applied in building functional tissues for human therapies. )

描述（由申请人提供）：严重缺乏功能性人体组织和器官掩埋可以排除大多数患有器官衰竭的患者的临床移植。此外，需要强大的人类模型来进行研究和药物开发。设计的人造器官和组织可以为器官移植和体外系统提供药物开发或疾病建模的替代方案或桥梁。 “经典”的生物材料和基于细胞外基质的组织工程面临着几个挑战，例如对生物材料的不利宿主反应，脚手架降解产物释放的有毒物质以及低细胞密度。脚手架 - 无组织工程旨在仅通过细胞和分泌的基质创建致密的3D组织（不使用聚合物和外源基质）。迄今为止，这种多细胞脚手架的“组织”是通过多种细胞类型的随机混合而创建的，任何组织都是细胞自组织1-5的结果。这些系统经常表现出高度可变的细胞形态发生（例如，可变的内皮细胞网络形成）以及组织核的坏死。在不含脚手架的系统中，受控组件在很大程度上没有探索。的确，组织工程中的一个中心未解决的问题是工程师需要控制绝对结构与“哄骗”生物学的程度，以通过形态发生自我组织到组织中。我们假设工程组织内的细胞的预定空间组织将促进细胞组织并最大化组织功能，我们将其定义为“指导的形态发生”。在此提案中，我们将研究空间信号如何通过空间控制工程无支架的多细胞组织的初始体系结构，如何在细胞社区之间驱动新兴的形态发生和组织组织。我们将开发一个平台为Micropatern 3D多细胞支架组织，然后研究预定义的组织结构如何决定组织功能和血管形态发生。我们将专门应用这些方法来研究3D多细胞组织结构的调节如何影响分化的肝细胞功能和组织以及工程无支架肝组织中的微血管形态发生。这项工作的最终目标是开发平台，以研究3D组织开发和功能中空间控制的多细胞相互作用，以建立工程肝组织的建筑“设计规范”。我们预计，这样的技术将极大地促进未来基于细胞的技术和工程组织的设计。 ） 公共卫生相关性：人工设计的组织（例如，肝脏）可以作为临床移植的器官取代以及研究和药物开发的测试系统。在这里，我们将开发新颖的工程工具，以研究自然在建造三维组织中如何组织不同类型的“蜂窝构建块”。这些知识可以应用于用于人类疗法的功能组织。 ）