课题基金 / 基金详情

Stem cells and phenotype specification in neural lineage development - Regulation of growth and differentiation in human stem cell systems

Stem cells and phenotype specification in neural lineage development - Regulation of growth and differentiation in human stem cell systems
神经谱系发育中的干细胞和表型规范 - 人类干细胞系统生长和分化的调节
批准号:
188562905
负责人:
Professor Dr. Jan Pruszak
金额:
$0.0万
依托单位国家:
德国
项目类别:
Independent Junior Research Groups
财政年份:
2011
资助国家:
德国
项目状态:
已结题
起止时间:
2010-12-31 至 2016-12-31

项目摘要

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中文摘要
翻译
在这个建议中概述的实验将显着提高目前的知识谱系规范和细胞间的相互作用在人类神经发育。神经谱系的发育(神经生成)包括许多高度微调的阶段和过渡。主要的研究工作旨在将多能干细胞(PSC)分化为生物医学相关的表型。然而,总的来说,我们对神经形态发生和表型特异性的信号通路和调控网络的理解仍然非常有限。目前的PSC定向分化的方法导致不适当的表型和异质性,控制不良的培养物,表明目前的体外方案忽视了细胞-细胞相互作用的方面,以及它们与适当的模式化,位置规范和形态发生的相关性。为了阐明这种自组织发育系统的细胞间通信的性质,有必要调查神经表面分子和分泌因子以及它们各自在神经表型的规范中的相互作用。我们假设,对hPSC衍生的神经细胞之间通过其各自的差异细胞表面特征与分泌因子/可扩散形态发生素组合的通信的机制理解将增强来自人胚胎和诱导多能干细胞的生理细胞类型的分化,这将使新的假设在神经胚胎学领域的制定和测试,并优化神经细胞的产生,用于生物医学。包括细胞治疗在内的应用。
英文摘要
The experiments outlined in this proposal will significantly enhance present knowledge of lineage specification and cell-cell interactions in human neural development. The development of the neural lineage (neuropoiesis) encompasses a number of highly fine-tuned stages and transitions. Major research efforts are aimed at the differentiation of pluripotent stem cells (PSCs) into biomedically relevant phenotypes. However, overall, our understanding of signaling pathways and regulatory networks underlying neural morphogenesis and phenotype specification has remained very limited. Current approaches of directed differentiation of PSCs result in inappropriate phenotypes and heterogenous, poorly controlled cultures, indicating that current in vitro protocols neglect the aspect of cell-cell interactions, and their relevance for appropriate patterning, positional specification and morphogenesis. To elucidate the nature of intercellular communication of such self-organized developmental systems, there is a need for investigating neural surface molecules and secreted factors as well as their respective interplay in the specification of neural phenotypes. We hypothesize that a mechanistic understanding of the communication between hPSC-derived neural cells via their respective differential cell surface signature in combination with secreted factors/diffusible morphogens will enhance the differentiation of physiological cell types from human embryonic and induced pluripotent stem cells, which will enable the formulation and testing of novel hypotheses in the fields of neuroembryology and optimized generation of neural cells for biomedical applications including cell therapy.
期刊论文(8)
专著(0)
科研奖励(0)
会议论文
DOI: 10.1371/journal.pone.0068519
发表时间: 2013-06-24
期刊: PLOS ONE
影响因子: 3.7
作者: [Turac, Gizem, Hindley, Christopher J., Pruszak, Jan]
通讯作者: Pruszak, Jan
DOI: 10.3727/096368912x654984
发表时间: 2013-01-01
期刊: CELL TRANSPLANTATION
影响因子: 3.3
作者: [Rath, Anika, Klein, Alexander, Nikkhah, Guido]
通讯作者: Nikkhah, Guido
国内基金
海外基金
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  • 项目类别:
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  • 资助金额:
    47.00万元
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    2023
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  • 批准号:
    82371634
  • 项目类别:
    面上项目
  • 资助金额:
    49.00万元
  • 批准年份:
    2023
  • 负责人:
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  • 批准号:
    82371379
  • 项目类别:
    面上项目
  • 资助金额:
    49.00万元
  • 批准年份:
    2023
  • 负责人:
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