Determinants of Self-Renewal, Differentiation, and Reprogramming of hESCs
Determinants of Self-Renewal, Differentiation, and Reprogramming of hESCs
批准号:
7515174
负责人:
James Alexander Thomson
金额:
$170.12万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-08-01 至 2013-07-31
中文摘要
产品说明:(申请人提供):了解人类胚胎干细胞(ES)如何能够无限制地增殖,同时保持分化为任何细胞类型的能力,是将本提案的三个单独项目联系起来的主题。项目1将使用一种新的质谱技术鉴定人类ES细胞中的新组蛋白修饰,该技术具有前所未有的鉴定和绘制翻译后蛋白修饰的能力。人类ES细胞中的组蛋白修饰将在启动子和由关键多能性因子直接调控的选定基因处进行全面鉴定。我们还将研究组蛋白H3变体在建立长期表观遗传记忆中的作用。这些研究将确定多能细胞中是否存在新的组蛋白密码,并确定组蛋白修饰在分化过程中如何动态变化。项目2研究了在人类ES细胞将eprogram分化的细胞转化为多能状态的时间窗口中发生的关键事件。我们以前曾报道,当骨髓细胞与人ES细胞融合时,骨髓细胞核重编程为ES细胞状态,表明ES细胞中的反式作用因子足以介导核重编程。我们的初步结果表明,过度表达的人ES细胞富集基因组合可以重编程骨髓细胞,该项目将优化这种重编程。这些项目的结合将提供对多能状态和细胞可以离开或返回该状态的基本过程的更多理解。这样的理解将是重要的移植和再生医学。
人类胚胎干细胞是特殊的,因为它们可以无限制地生长,并可以产生所有其他类型的细胞。在这里,我们将试图了解为什么人类ES细胞具有这种显着的发育潜力,并开发条件将具有更有限潜力的细胞转化为ES细胞。这种重新编程对移植和再生医学有影响。
英文摘要
DESCRIPTION: (provided by applicant): Understanding how human embryonic stem (ES) cells can proliferate without limit and yet retain the ability to differentiate to any cell type is the theme that links the three individual projects of this proposal. Project 1 will identify novel histone modifications in human ES cells using a new mass spectrometry technique that allows an unprecedented ability to identify and map posttranslational protein modifications. Histone modifications in human ES cells will be identified globally, at promoters, and at select genes directly regulated by critical pluripotency factors. We will also examine the role of histone H3 variants in establishing long-term epigenetic memory. These studies will determine whether there is a novel histone code in pluripotent cells and determine how histone modifications change dynamically during differentiation. Project 2 examines the critical events that occur in the window of time during which human ES cells commit eprogram differentiated cells to a pluripotent state. We have previously reported that when myeloid cells are fused with human ES cells, the myeloid nucleus is reprogrammed to an ES cell state, indicating that transacting factors in ES cells are sufficient to mediate nuclear reprogramming. Our preliminary results suggest that over expressing combinations of human ES cell-enriched genes can reprogram myeloid cells, and this project will optimize this reprogramming. The combination of these projects will provide an increased understanding of the pluripotent state and the basic processes by which a cell can leave or return to that state. Such an understanding will be important to transplantation and regenerative medicine.
Lay Description: Human ES cells are special because they can grow without limit and can give rise to all other cell types. Here we will try to understand why human ES cells have this remarkable developmental potential, and develop conditions to convert a cell with a more limited potential to an ES cell. Such reprogramming has implications for transplantation and regenerative medicine.
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Human iPS/ES Cell-Based Models for Predictive Neural Toxicity and Teratogenicity
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Self-Renewal and Differentiation: Molecular Events that Commit ES Cells to Exit t
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批准号:8381275
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Human iPS/ES Cell-Based Models for Predictive Neural Toxicity and Teratogenicity
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WNPRC STEM CELL RESOURCE
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批准号:8173102
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资助金额:$10.33万
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批准号:8323131
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负责人:James Alexander Thomson
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依托单位:
Midwest Progenitor Cell Consortium
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批准号:8661226
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资助金额:$114.23万
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财政年份:2009
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负责人:James Alexander Thomson
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依托单位:
Midwest Progenitor Cell Consortium
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项目类别:
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资助金额:$105.88万
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财政年份:2009
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负责人:James Alexander Thomson
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依托单位:
Midwest Progenitor Cell Consortium
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批准号:8722409
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项目类别:
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资助金额:$5.27万
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财政年份:2009
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负责人:James Alexander Thomson
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依托单位:
Midwest Progenitor Cell Consortium
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批准号:7939693
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资助金额:$107.45万
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财政年份:2009
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负责人:James Alexander Thomson
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依托单位:
Determinants of Self-Renewal, Differentiation, and Reprogramming of hESCs
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批准号:7932409
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项目类别:
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资助金额:$43.55万
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Midwest Progenitor Cell Consortium
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Midwest Progenitor Cell Consortium
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批准号:7820075
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资助金额:$110.13万
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负责人:James Alexander Thomson
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IMPROVED LENTIVIRAL VECTORS FOR PRIMATE EMBRYONIC STEM CELLS
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