Systematic Characterization of an Aging Stem Cell Niche

衰老干细胞生态位的系统表征

• 批准号: 8885417
• 负责人: Michael Buszczak
• 金额: $ 33.11万
• 依托单位: UT SOUTHWESTERN MEDICAL CENTER
• 依托单位国家: 美国
• 财政年份: 2015
• 资助国家: 美国
• 起止时间: 2015-04-15 至 2020-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8885417
• 关键词: Adult; Age; Aging; Aging-Related Process; Bioinformatics; Biological Models; Cell Aging; Cell Maintenance; Cell physiology; Cells; Colony-Forming Units Assay; Complex; Data; Daughter; Development; Drosophila genus; Drug Metabolic Detoxication; Enzymes; Equilibrium; Evaluation; Female; Fostering; Gene Expression; Gene Expression Profile; Genes; Goals; Health; Homeostasis; Injury; Invertebrates; Life; Maintenance; Massive Parallel Sequencing; Medical; Messenger RNA; Methods; Microbe; Modeling; Molecular Genetics; Molecular Probes; Molecular Target; Natural Immunity; Natural regeneration; Normal tissue morphology; Organism; Output; Ovarian; Ovary; Pathway interactions; Phenotype; Population; Protocols documentation; RNA; Route; Science; Set protein; Signal Transduction; Signaling Molecule; Stem cells; Superoxide Dismutase; System; Techniques; Testing; Time; Tissues; Work; age related; aged; antimicrobial; base; biological adaptation to stress; cell age; gain of function; gene function; germline stem cells; human disease; in vivo; insight; loss of function; prevent; programs; protein function; public health relevance; repaired; research study; response; self-renewal; stem; stem cell biology; stem cell differentiation; stem cell niche; therapy design/development; transcriptome sequencing

 DESCRIPTION (provided by applicant): The inability of stem cells to support tissue homeostasis and repair underlies many age- related phenotypes. Specialized microenvironments called niches help maintain proper tissue homeostasis by controlling the balance between stem cell self-renewal and the differentiation of their daughters. However, the mechanisms that govern the formation, size and signaling output of in vivo niches remain poorly understood. Our long-term goal is to identify and characterize the factors that regulate niche function in vivo. Stem cells and their supportive microenvironments have often proven difficult to identify in vivo in many mammalian tissues. As a result, much of our current understanding of niches stems from the study of invertebrate models. In this proposal, we seek to build upon previous efforts that have established the Drosophila ovary as a powerful system with which to study stem cell niche aging. We propose to use state of the art cell purification and massive parallel sequencing techniques to systematically characterize the transcriptional profile of niche cells and their immediate neighbors. Moreover, we seek to genetically test the functional relevance of gene expression changes that occur within the niche during aging by using powerful cell-specific loss-of-function and gain-of- function techniques. We have established an operational pipeline for conducting all the experiments outlined under this proposal. Already, our preliminary data suggests that niches carry out previously unrecognized functions that are likely to be important for stem cell health and maintenance over time. In Aim 1, we seek to comprehensively and quantitatively assess changes in gene expression within the Drosophila ovarian germline stem cell niche during aging. In Aim 2, we will build upon our preliminary data and test whether niches help to protect stem cells from microbes that can be introduced through natural routes or via injury. Finally in Aim 3, we probe the molecular mechanisms by which a superoxide dismutase helps to prolong proper niche function late in life. We believe this comprehensive analysis of in vivo niche function during the course of aging will provide key insights into why stem cell activity declines with age and will reveal new molecular targets for the development of therapies designed to foster continued tissue homeostasis and regeneration in aging organisms.

 描述(由申请者提供)：干细胞不能支持组织动态平衡和修复是许多年龄相关表型的基础。专门的微环境被称为生态位，通过控制干细胞自我更新和子代分化之间的平衡，帮助维持适当的组织动态平衡。然而，控制体内生态位的形成、大小和信号输出的机制仍然知之甚少。我们的长期目标是识别和表征体内调节利基功能的因素。干细胞及其支持微环境经常被证明在许多哺乳动物组织中很难在体内识别。因此，我们目前对生态位的大部分理解都源于对无脊椎动物模型的研究。在这项建议中，我们寻求建立在以前的努力的基础上，建立了果蝇卵巢作为一个强大的系统，用来研究干细胞的生态位老化。我们建议使用最先进的细胞纯化和大规模并行测序技术来系统地表征利基细胞及其近邻的转录图谱。此外，我们试图通过使用强大的细胞特异性功能丧失和功能获得技术来测试在衰老过程中发生的利基内基因表达变化的功能相关性。我们已经为进行这项提议中概述的所有实验建立了一条可操作的管道。我们的初步数据已经表明，随着时间的推移，壁龛执行着以前未被认识到的功能，这些功能可能对干细胞的健康和维持很重要。在目标1中，我们试图全面和定量地评估果蝇卵巢生殖系干细胞在衰老过程中基因表达的变化。在目标2中，我们将以我们的初步数据为基础，测试生态位是否有助于保护干细胞免受可通过自然途径或通过伤害进入的微生物的侵袭。最后，在目标3中，我们探索了超氧化物歧化酶帮助延长生命后期适当的生态位功能的分子机制。我们相信，这种对衰老过程中体内生态位功能的全面分析将为干细胞活性随着年龄增长而下降的原因提供关键的见解，并将揭示新的分子靶点，用于开发旨在促进衰老生物体持续组织动态平衡和再生的治疗方法。