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Regeneration of the damaged central nervous system through reprogramming technology: Basic concepts and potential application for cell replacement therapy

机译:通过重编程技术再生受损的中枢神经系统:细胞替代疗法的基本概念和潜在应用

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摘要

Neural stem cell (NSC) transplantation provides a new approach for the repair of damage to the central nervous system (CNS), including that resulting from cerebral infarction and spinal cord injury (SCI). In the past, there were no reputable means of converting non-neural somatic cells into neural cells. This status was overturned by the establishment of induced pluripotent stem (iPS) cells, which have pluripotency akin to that of embryonic stem (ES) cells and can differentiate into most cells of the three germ layers. If differentiated somatic cells could be reprogrammed into iPS cells, and if these iPS cells could be induced to differentiate once again, it would be theoretically possible to obtain a large number of neural cells. However, this is not yet feasible due to the limitations of existing stem cell technology. Induction of neural cells from iPS cells is currently hindered by two distinct problems: 1) the preparation of specific types of targeted neural cells requires extensive cell culture, and 2) tumors are likely to form due to the presence of residual undifferentiated cells following transplantation of the induced cells. By contrast, direct induction methods permit the generation of target cells from somatic cells without the transitional iPS cell stage. This review outlines the present-day status of research surrounding the direct induction of NSCs from somatic cells, as well as the perspectives for the future clinical application of this technique for cell replacement therapy following CNS injury. (C) 2012 Elsevier Inc. All rights reserved.
机译:神经干细胞(NSC)移植提供了一种修复中枢神经系统(CNS)损伤的新方法,其中包括由脑梗死和脊髓损伤(SCI)引起的损伤。过去,没有将非神经体细胞转化为神经细胞的著名方法。这种状态被诱导多能干(iPS)细胞的建立所推翻,该细胞具有与胚胎干(ES)细胞相似的多能性,并且可以分化为三个胚层的大多数细胞。如果可以将分化的体细胞重新编程为iPS细胞,并且如果可以诱导这些iPS细胞再次分化,那么理论上就有可能获得大量的神经细胞。然而,由于现有干细胞技术的局限性,这尚不可行。目前,从iPS细胞诱导神经细胞受到两个明显的问题的阻碍:1)制备特定类型的靶向神经细胞需要大量细胞培养,并且2)移植后由于存在未分化的残余细胞而可能形成肿瘤诱导细胞。相比之下,直接诱导方法允许从体细胞生成靶细胞而无需过渡iPS细胞阶段。这篇综述概述了从体细胞直接诱导NSC的研究现状,以及该技术在中枢神经系统损伤后进行细胞替代治疗的未来临床应用前景。 (C)2012 Elsevier Inc.保留所有权利。

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