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Stem cells, regenerative medicine, and animal models of disease

机译:干细胞,再生医学和疾病动物模型

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The field of stem cell biology and regenerative medicine is rapidly moving toward translation to clinical practice, and in doing so has become even more dependent on animal donors and hosts for generating cellular reagents and assaying their potential therapeutic efficacy in models of human disease. Advances in cell culture technologies have revealed a remarkable plasticity of stem cells from embryonic and adult tissues, and transplantation models are now needed to test the ability of these cells to protect at-risk cells and replace cells lost to injury or disease. With such a mandate, issues related to acceptable sources and controversial (e.g., chimeric) models have challenged the field to provide justification of their potential efficacy before the passage of new restrictions that may curb anticipated breakthroughs. Progress from the use of both in vitro and in vivo regenerative medicine models already offers hope both for the facilitation of stem cell phenotyping in recursive gene expression profile models and for the use of stem cells as powerful new therapeutic reagents for cancer, stroke, Parkinson's, and other challenging human diseases that result in movement disorders. This article describes research in support of the following three objectives: (1) To discover the best stem or progenitor cell in vitro protocols for isolating, expanding, and priming these cells to facilitate their massive propagation into just the right type of neuronal precursor cell for protection or replacement protocols for brain injury or disease, including those that affect movement such as Parkinson's disease and stroke; (2) To discover biogenic factors--compounds that affect stem/progenitor cells (e.g., from high-throughput screening and other bioassay approaches)--that will encourage reactive cell genesis, survival, selected differentiation, and restoration of connectivity in central nervous system movement and other disorders; and (3) To establish the best animal models of human disease and injury, using both small and large animals, for testing new regenerative medicine therapeutics.
机译:干细胞生物学和再生医学领域正迅速向翻译过渡到临床实践,并且在此过程中,它已越来越依赖于动物供体和宿主来产生细胞试剂并测定其在人类疾病模型中的潜在治疗功效。细胞培养技术的进步揭示了来自胚胎和成年组织的干细胞具有显着的可塑性,现在需要移植模型来测试这些细胞保护高危细胞并替换因损伤或疾病而丢失的细胞的能力。有了这样的授权,与可接受的来源和有争议的(例如,嵌合体)模型有关的问题已经挑战了该领域,在通过可能限制预期突破的新限制之前,提供其潜在效力的理由。利用体外和体内再生医学模型取得的进展已经为促进干细胞表型在递归基因表达谱模型中的应用以及将干细胞用作治疗癌症,中风,帕金森氏症的有力新药提供了希望。以及其他导致运动异常的具有挑战性的人类疾病。本文介绍了支持以下三个目标的研究:(1)发现最佳的干细胞或祖细胞体外实验方案,以分离,扩增和引发这些细胞,以促进其大规模繁殖,从而成为正确的神经元前体细胞。脑损伤或疾病的保护或替代方案,包括那些影响运动的方案,如帕金森氏病和中风; (2)发现生物因子-影响干/祖细胞的化合物(例如,通过高通量筛选和其他生物测定方法)-会鼓励反应性细胞的发生,存活,选择性分化以及中枢神经系统连接性的恢复。系统运动和其他障碍; (3)使用大小动物建立人类疾病和伤害的最佳动物模型,以测试新的再生医学疗法。

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