Epigenetic Effect of the Microenvironment on Stem Cell Plasticity and Function

微环境对干细胞可塑性和功能的表观遗传效应

• 批准号: 7460702
• 负责人: MARY J.C. HENDRIX
• 金额: $ 33.1万
• 依托单位: LURIE CHILDREN'S HOSPITAL OF CHICAGO
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-07-03 至 2012-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7460702
• 关键词: 3-Dimensional; Affect; Biological; Blood Vessels; Cell Fate Control; Cell Line; Cells; Characteristics; Chick Embryo; Communication; Complex; Cues; Data; Development; Disease; Embryo; Epigenetic Process; Gene Expression; Gene Proteins; Genes; Genotype; Goals; Grant; Human; Image; In Situ; Knowledge; Laboratories; Limb structure; Maintenance; Malignant Neoplasms; Melanoma Cell; Metastatic Melanoma; Modeling; Molecular; Multipotent Stem Cells; Mus; Neural Crest; Neural Crest Cell; Neurons; Nodal; Notch Signaling Pathway; Nude Mice; Pathway interactions; Phenotype; Plastics; Play; Population; Process; Property; Qualifying; Research Personnel; Role; Signal Pathway; Signal Transduction; Stem cells; Study models; Testing; Tissues; Translating; Transplantation; Tumor Cell Line; UC06; WA01 cell line; WA09 Cell Line; Wound Healing; base; cancer cell; comparative; concept; design; extracellular; human embryonic stem cell; insight; laser capture microdissection; melanocyte; melanoma; neoplastic cell; notch protein; novel; novel therapeutics; precursor cell; programs; reconstitution; relating to nervous system; tumor; tumor progression

DESCRIPTION (provided by applicant): One of the most devastating diseases to manage is metastatic melanoma, where the evidence of stem cell subpopulations is starting to emerge. Comparative global gene analyses of aggressive human melanoma cell lines and tumors have revealed the expression of genes associated with multiple cellular phenotypes and precursor stem cells. These findings support the premise that aggressive melanoma cells revert to a multipotent, plastic phenotype. Key to identifying the molecular mechanisms underlying tumor cell plasticity is to elucidate the unique role the microenvironment plays in this process. Most noteworthy are the data we have generated showing the reprogramming of subpopulations (possibly the stem cells) of multipotent metastatic melanoma cells to a melanocyte-like phenotype by the embryonic microenvironment(s) of hESCs and chick neural crest-rich regions. Based on these observations, we propose to test the central hypothesis that the embryonic microenvironments associated with hESCs (Wa01. Wa09 and UC06) and chick neural crest-rich region(s) - contain informational cues with the potential to epigenetically reprogram the genotype and phenotype of human metastatic multipotent melanoma cells exposed to them. Our long term goal is to understand the biological mechanisms underlying the bi-directional communication between stem cells and their microenvironment(s) that ultimately result in cell fate determinations. Our short term goal is to identify the biological and molecular parameters associated with the epigenetic reprogramming of multipotent metastatic melanoma cells exposed to specific hESC environmental cues. Using unique, 3-D organotypic models and chick embryos, together with functional analysis, 4-D imaging, laser capture microdissection, and epigenetic analysis, we propose to: Unchanged Aim 1: Determine the epigenetic influence of the 3-D microenvironment(s) of hESCs for their potential to reprogram the genotype and phenotype of human metastatic multipotent melanoma cells. Revised Aim 2: Identify the molecular basis for the epigenetic reprogramming of the genotype and phenotype of the affected multipotent melanoma cell populations exposed to various hESC 3-D microenvironments, with particular focus on the Nodal signaling pathway. Revised Aim 3: Investigate the developmental plasticity of multipotent melanoma cell populations in an embryonic chick model - to determine the biological relevance of the Nodal signaling pathway involved in stem cell plasticity and the control of cell fate determination and reprogramming of the metastatic phenotype. Lay Summary: At the completion of these studies, we expect to gain new insights into the biological properties of human embryonic and multipotent metastatic melanoma cells with stem cell properties that could be translated for novel therapeutic applications.

描述(申请人提供)：转移性黑色素瘤是最具破坏性的疾病之一，干细胞亚群的证据开始出现。对侵袭性人类黑色素瘤细胞系和肿瘤的比较全球基因分析揭示了与多种细胞表型和前体干细胞相关的基因表达。这些发现支持侵袭性黑色素瘤细胞回复到多潜能的可塑性表型的前提。确定肿瘤细胞可塑性的分子机制的关键是阐明微环境在这一过程中所起的独特作用。最值得注意的是我们产生的数据显示，多潜能转移性黑色素瘤细胞的亚群(可能是干细胞)被胚胎微环境(S)重新编程为黑素细胞样表型。基于这些观察，我们建议检验中心假设，胚胎微环境与hESCs有关(Wa01。WA09和UC06)和鸡神经脊富集区(S)包含信息线索，有可能对暴露于它们的人转移性多潜能黑色素瘤细胞的基因型和表型进行表观遗传重新编程。我们的长期目标是了解干细胞及其微环境之间双向交流的生物学机制(S)，这最终导致细胞命运的决定。我们的短期目标是确定与暴露于特定hESC环境线索的多潜能转移性黑色素瘤细胞的表观遗传重编程相关的生物学和分子参数。使用独特的3-D器官模型和鸡胚，结合功能分析、4-D成像、激光捕获显微解剖和表观遗传学分析，我们建议：不变的目标1：确定hESCs的3-D微环境(S)对其重新编程人类转移性多潜能黑色素瘤细胞的基因和表型的潜力的表观遗传学影响。修订的目标2：确定暴露在不同hESC 3-D微环境中的受影响的多潜能黑色素瘤细胞群体的表观遗传重新编程的基因和表型的分子基础，特别关注Nodal信号通路。修订的目标3：在鸡胚胎模型中研究多潜能黑色素瘤细胞群体的发育可塑性-确定参与干细胞可塑性的Nodal信号通路的生物学相关性，以及控制细胞命运决定和转移表型的重新编程。Lay概要：在这些研究完成后，我们希望对具有干细胞特性的人类胚胎和多潜能转移性黑色素瘤细胞的生物学特性有新的见解，这些特性可以转化为新的治疗应用。