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Advances in human stem cell therapies: pre-clinical studies and the outlook for central nervous system regeneration

机译:人体干细胞疗法的进展:临床前研究和中枢神经系统再生的前景

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摘要

Cell transplantation has come to the forefront of regenerative medicine alongside the discovery and application of stem cells in both research and clinical settings. There are several types of stem cells currently being used for pre-clinical regenerative therapies, each with unique characteristics, benefits and limitations. This brief review will focus on recent basic science advancements made with embryonic stem cells and induced pluripotent stem cells. Both embryonic stem cells and induced pluripotent stem cells provide platforms for new neurons to replace dead and/or dying cells following injury. Due to their capacity for reprogramming and differentiation into any neuronal type, research in preclinical rodent models has shown that embryonic stem cells and induced pluripotent stem cells can integrate, survive and form connections in the nervous system similar to de novo cells. Going forward however, there are some limitations to consider with the use of either stem cell type. Ethically, embryonic stem cells are not an ideal source of cells, genetically, induced pluripotent stem cells are not ideal in terms of personalized treatment for those with certain genetic diseases the latter of which may guide regenerative medicine away from personalized stem cell based therapies and into optimized stem cell banks. Nonetheless, the potential of these stem cells in central nervous system regenerative therapy is only beginning to be appreciated. For example, through genetic modification, stem cells serve as ideal platforms to reintroduce missing or downregulated molecules into the nervous system to further induce regenerative growth. In this review, we highlight the limitations of stem cell based therapies whilst discussing some of the means of overcoming these limitations.
机译:在研究和临床环境中发现和应用干细胞的发现和应用,细胞移植伴有再生医学的最前沿。目前有几种类型的干细胞用于临床前再生疗法,每个干细胞具有独特的特征,益处和限制。本简要综述将重点关注近期用胚胎干细胞和诱导多能干细胞进行的基础科学进步。胚胎干细胞和诱导多能干细胞均为新神经元提供损伤后造成死亡和/或染色细胞的平台。由于它们对任何神经元类型的重新编程和分化的能力,临床前啮齿动物模型的研究表明,胚胎干细胞和诱导多能干细胞可以整合,存活和形成与De Novo细胞类似的神经系统中的连接。然而,通过使用干细胞类型需要考虑一些局限性。道德上,胚胎干细胞不是理想的细胞来源,遗传上,在具有某些遗传疾病的人的个性化治疗方面,诱导多能干细胞的理想下降可能导致再生药物远离个性化的干细胞的疗法和进入优化的干细胞库。尽管如此,这些干细胞在中枢神经系统中的潜力才能开始欣赏疗法。例如,通过遗传修饰,干细胞用作将缺失或下调分子重新引入神经系统的理想平台,以进一步诱导再生生长。在本综述中,我们突出了基于干细胞的疗法的局限性,同时讨论了一些克服了这些限制的手段。

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