神经系统疾病的潜在治疗方法综述:人类胚胎干细胞治疗。

IF 1.5 Q4 CELL BIOLOGY
American journal of stem cells Pub Date : 2017-04-15 eCollection Date: 2017-01-01
Geeta Shroff, Jyoti Dhanda Titus, Rhea Shroff
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引用次数: 0

摘要

第一个人类胚胎干细胞(hESC)系是在90年代末开发的。hESCs能够无限增殖并分化为所有三种胚胎胚层。此外,hESC细胞系分化为神经前体细胞和神经元、星形胶质细胞和少突胶质细胞,在治疗脊髓损伤(SCI)、脑瘫(CP)、帕金森病(PD)等多种无法治愈的神经系统疾病方面显示出潜力。在这篇综述中,我们将讨论hESCs在神经系统疾病治疗中的研究和治疗应用的全球情况。接下来,我们将讨论一种独特的hESC细胞系的发展,它与其他可用的hESC细胞系有何不同,以及它在治疗神经系统疾病中的应用。hESCs是在符合良好实验室规范、良好组织规范和良好生产规范的实验室中从处于前祖细胞状态的神经元和非神经元祖细胞混合物中分离出来的。卵裂球细胞是hESCs的来源,无异种培养在hESCs的临床治疗应用中被证明是更安全有效的。所有患者的病情均有显著改善,无严重不良事件发生。本研究得出结论,hESC系可扩展并可用于治疗各种神经系统疾病,如SCI、CP和PD。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A review of the emerging potential therapy for neurological disorders: human embryonic stem cell therapy.

A review of the emerging potential therapy for neurological disorders: human embryonic stem cell therapy.

A review of the emerging potential therapy for neurological disorders: human embryonic stem cell therapy.

A review of the emerging potential therapy for neurological disorders: human embryonic stem cell therapy.

The first human embryonic stem cell (hESC) line was developed in the late nineties. hESCs are capable of proliferating indefinitely and differentiate into all the three embryonic germ layers. Further, the differentiation of hESC lines into neural precursor cells and neurons, astrocytes and oligodendrocytes showed their potential in treating several incurable neurological disorders such as spinal cord injury (SCI), cerebral palsy (CP), Parkinson's disease (PD). In this review, we will discuss the global scenario of research and therapeutic use of hESCs in the treatment of neurological disorders. Following this, we will discuss the development of a unique hESC line, how it differs from the other available hESC lines and its use in the treatment of neurological disorders. hESCs were isolated from mixture of neuronal and non-neuronal progenitor cells in their pre progenitor state in a Good Laboratory Practices, Good Tissue Practices and Good Manufacturing Practices compliant laboratory. Blastomere cells have served as a source to derive the hESCs and the xeno-free culture was demonstrated to be more safe and effective in clinical therapeutic application of hESCs. All the patients showed a remarkable improvement in their conditions and no serious adverse events were reported. This study concluded that hESC lines could be scalable and used in the treatment of various neurological disorders such as SCI, CP, and PD.

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