Isolation and Characterization of Intestinal Stem Cells

描述(由申请人提供)：小肠为成人干细胞的研究提供了一个最优雅的系统--这些细胞为再生医学带来了巨大的希望。遗传学研究揭示了几个在肠道干细胞(ISCs)调节中发挥作用的关键信号通路。这为理解ISCs的更新、自我修复和分化为多种肠道细胞类型的能力提供了重要的见解。然而，由于无法在体内(在活组织内)或体外(在活组织外的受控环境中)分离和移植ISCs以进行深入研究，进一步的进展受到阻碍。本研究项目旨在解决ISC研究中的这一障碍，包括开发新的可靠的ISC分离、体外培养和体内功能鉴定方法。 ISC的分离将通过使用荧光标记蛋白和其他膜表面蛋白来分类和验证已知在肠道干细胞中表达的基因来完成。体外培养将通过添加对支持ISC增殖至关重要的关键因素到Matrigel或隐窝球体的三维培养来完成。功能鉴定将通过将分离的ISCs注射到照射后的隐窝球中，然后将嵌合球移植到体内微环境中来完成，以表征ISC的存活、自我更新、增殖和血统承诺。 如果这一目标能够实现，它不仅将为推进对ISC行为的研究开辟道路，也将为治疗肠道疾病开辟道路，在肠道疾病中，ISC驱动的组织再生是必不可少的，并将为筛选针对癌症干细胞的药物开辟道路。识别、分离和鉴定ISCs的能力对于治疗的进步，特别是组织替代，以及对了解癌症的发展、预防和治疗至关重要。 与公共健康相关：在美国，消化系统疾病的直接费用总计超过850亿美元，间接费用超过230亿美元。有证据表明，肠道干细胞(ISCs)参与了许多病例--从克罗恩病到结肠炎再到癌症。这项研究将增加对ISC生物学的了解，这些知识可用于提高治疗效果，改善患者预后，并最终影响消化系统疾病的公共健康负担

DESCRIPTION (provided by applicant): The small intestine provides a most elegant system for the study of adult stem cells -- cells which hold great promise for regenerative medicine. Genetic studies have revealed several key signaling pathways that play a role in the regulation of intestinal stem cells (ISCs). This has provided important insight into understanding the capacity of ISCs for renewal and self-repair and differentiation into multiple intestinal cell types. However, further progress is impeded by the inability to isolate and transplant ISCs for advanced study either in vivo (within living tissue) or in vitro (within a controlled environment outside of a living organism). This research project proposes to address this barrier to ISC research, including the development of novel and reliable methods for ISC isolation, in vitro culture, and in vivo functional characterization. ISC isolation will be accomplished by using fluorescent label protein and other membrane surface proteins to sort and verify cells by genes known to be expressed in intestinal stem cells. In vitro culture will be accomplished by adding key factors that are important for supporting ISC proliferation into Matrigel or 3-dimensional culture of crypt sphere. Functional characterization will be accomplished by injecting isolated ISCs into the irradiated crypt sphere and then transplanting the chimeric sphere to an in vivo microenvironment to characterize ISC survival, self-renewal, proliferation, and lineage commitment. If this goal can be achieved, it will open avenues not only for advancing the study of ISC behavior, but also for treating intestinal disorders in which ISC-driven tissue regeneration is essential and for screening drugs to target on cancer stem cells. The ability to identify and isolate and characterize ISCs is critical for therapeutic advancements, especially tissue replacement, and for understanding cancer development, prevention and cure. PUBLIC HEALTH RELEVANCE: The cost of digestive diseases in the U.S. collectively exceeds $85 billion in direct and $23 billion in indirect expenses. Evidence indicates intestinal stem cells (ISCs) are involved in many cases -- from Crohn's to colitis to cancer. This research will increase knowledge of ISC biology, which can be applied to enhance treatment efficacies, improve patient outcomes, and ultimately, impact the public health burden of digestive diseases