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Cell Viability of Human Embryonic Stem Cells Stored for a Period of 9 Years.储存9年的人类胚胎干细胞的细胞活力
Exp Clin Transplant. 2017 Jun;15(3):344-349. doi: 10.6002/ect.2016.0097. Epub 2016 Dec 12.
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Morphogenesis of human embryonic stem cells into mature neurons under culture conditions.在培养条件下人类胚胎干细胞向成熟神经元的形态发生
World J Exp Med. 2016 Nov 20;6(4):72-79. doi: 10.5493/wjem.v6.i4.72.
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Human embryonic stem cells in the treatment of patients with spinal cord injury.人类胚胎干细胞在脊髓损伤患者治疗中的应用。
Ann Neurosci. 2015 Oct;22(4):208-16. doi: 10.5214/ans.0972.7531.220404.
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Safety of human embryonic stem cells in patients with terminal/incurable conditions- a retrospective analysis.终末期/无法治愈疾病患者中人类胚胎干细胞的安全性——一项回顾性分析
Ann Neurosci. 2015 Jul;22(3):132-8. doi: 10.5214/ans.0972.7531.220303.
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Human embryonic stem cell cultivation: historical perspective and evolution of xeno-free culture systems.人类胚胎干细胞培养:无血清培养系统的历史回顾与演变
Reprod Biol Endocrinol. 2015 Feb 22;13:9. doi: 10.1186/s12958-015-0005-4.
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X chromosome inactivation in human parthenogenetic embryonic stem cells following prolonged passaging.长时间传代后人孤雌生殖胚胎干细胞中的X染色体失活
Int J Mol Med. 2015 Mar;35(3):569-78. doi: 10.3892/ijmm.2014.2044. Epub 2014 Dec 18.
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Therapeutic potential of human embryonic stem cell transplantation in patients with cerebral palsy.人胚胎干细胞移植治疗脑瘫患者的潜力。
J Transl Med. 2014 Dec 12;12:318. doi: 10.1186/s12967-014-0318-7.
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Wrongful termination: lessons from the Geron clinical trial.不当解雇:来自杰龙公司临床试验的教训。
Stem Cells Transl Med. 2014 Dec;3(12):1398-401. doi: 10.5966/sctm.2014-0147. Epub 2014 Oct 8.
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SDF-1/CXCR4 axis in Tie2-lineage cells including endothelial progenitor cells contributes to bone fracture healing.SDF-1/CXCR4 轴在包括内皮祖细胞在内的 Tie2 谱系细胞中促进骨骨折愈合。
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A 3D sphere culture system containing functional polymers for large-scale human pluripotent stem cell production.一种含有功能聚合物的 3D 球型培养体系,用于大规模生产人类多能干细胞。
Stem Cell Reports. 2014 Apr 24;2(5):734-45. doi: 10.1016/j.stemcr.2014.03.012. eCollection 2014 May 6.

神经疾病新兴潜在疗法综述:人类胚胎干细胞疗法

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

作者信息

Shroff Geeta, Dhanda Titus Jyoti, Shroff Rhea

机构信息

Department of Stem Cell Therapy, Nutech Mediworld, H-8, Green Park ExtensionNew Delhi 110016, India.

Department of Administration, Nutech Mediworld, H-8, Green Park ExtensionNew Delhi 110016, India.

出版信息

Am J Stem Cells. 2017 Apr 15;6(1):1-12. eCollection 2017.

PMID:28533935
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5435646/
Abstract

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.

摘要

第一条人类胚胎干细胞(hESC)系于九十年代后期建立。hESC能够无限增殖,并分化为所有三个胚胎胚层。此外,hESC系向神经前体细胞、神经元、星形胶质细胞和少突胶质细胞的分化显示出其在治疗多种无法治愈的神经系统疾病(如脊髓损伤(SCI)、脑瘫(CP)、帕金森病(PD))方面的潜力。在本综述中,我们将讨论hESC在神经系统疾病治疗中的研究和治疗应用的全球情况。在此之后,我们将讨论一种独特的hESC系的建立、它与其他现有hESC系的不同之处以及它在神经系统疾病治疗中的应用。hESC是在一个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,从处于祖细胞前期状态的神经元和非神经元祖细胞混合物中分离出来的。卵裂球细胞已作为获取hESC的来源,并且无动物源培养在hESC的临床治疗应用中被证明更安全有效。所有患者的病情都有显著改善,且未报告严重不良事件。本研究得出结论,hESC系可进行规模化培养,并用于治疗各种神经系统疾病,如SCI、CP和PD。