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本文引用的文献

1
Preterm human amnion epithelial cells have limited reparative potential.人羊膜上皮细胞的再生潜力有限。
Placenta. 2013 Jun;34(6):486-92. doi: 10.1016/j.placenta.2013.03.010. Epub 2013 Apr 15.
2
Amniotic fluid and placental membranes: unexpected sources of highly multipotent cells.羊膜和胎盘膜:具有多能性的细胞的意外来源。
Semin Reprod Med. 2013 Jan;31(1):62-8. doi: 10.1055/s-0032-1331799. Epub 2013 Jan 17.
3
Human amnion epithelial cells mediate lung repair by directly modulating macrophage recruitment and polarization.人羊膜上皮细胞通过直接调节巨噬细胞募集和极化来介导肺修复。
Cell Transplant. 2014 Mar;23(3):319-28. doi: 10.3727/096368912X661409. Epub 2013 Jan 2.
4
Human amnion epithelial cells induced to express functional cystic fibrosis transmembrane conductance regulator.诱导人羊膜上皮细胞表达功能性囊性纤维化跨膜电导调节剂。
PLoS One. 2012;7(9):e46533. doi: 10.1371/journal.pone.0046533. Epub 2012 Sep 28.
5
Human amniotic epithelial cell transplantation induces markers of alternative macrophage activation and reduces established hepatic fibrosis.人羊膜上皮细胞移植诱导替代型巨噬细胞活化标志物的产生,并减轻已建立的肝纤维化。
PLoS One. 2012;7(6):e38631. doi: 10.1371/journal.pone.0038631. Epub 2012 Jun 14.
6
Amnion epithelial cells as a candidate therapy for acute and chronic lung injury.羊膜上皮细胞作为急性和慢性肺损伤的候选治疗方法。
Stem Cells Int. 2012;2012:709763. doi: 10.1155/2012/709763. Epub 2012 Apr 11.
7
Human amnion epithelial cells do not abrogate pulmonary fibrosis in mice with impaired macrophage function.人羊膜上皮细胞不能减轻巨噬细胞功能受损的小鼠的肺纤维化。
Cell Transplant. 2012;21(7):1477-92. doi: 10.3727/096368911X601028.
8
Human amnion epithelial cells prevent bleomycin-induced lung injury and preserve lung function.人羊膜上皮细胞可预防博来霉素诱导的肺损伤并维持肺功能。
Cell Transplant. 2011;20(6):909-23. doi: 10.3727/096368910X543385. Epub 2010 Nov 19.
9
Amnion epithelial cell isolation and characterization for clinical use.用于临床的羊膜上皮细胞分离与鉴定
Curr Protoc Stem Cell Biol. 2010 Apr;Chapter 1:Unit 1E.6. doi: 10.1002/9780470151808.sc01e06s13.
10
Novel neurotrophic factor secreted by amniotic epithelial cells.羊膜上皮细胞分泌的新型神经营养因子。
Biocell. 2009 Aug;33(2):81-9.

用于临床应用的人羊膜上皮细胞的分离、冷冻保存及培养

Isolation, cryopreservation and culture of human amnion epithelial cells for clinical applications.

作者信息

Murphy Sean V, Kidyoor Amritha, Reid Tanya, Atala Anthony, Wallace Euan M, Lim Rebecca

机构信息

Wake Forest Institute for Regenerative Medicine, Wake Forest University Health Sciences;

Wake Forest Institute for Regenerative Medicine, Wake Forest University Health Sciences.

出版信息

J Vis Exp. 2014 Dec 21(94):52085. doi: 10.3791/52085.

DOI:10.3791/52085
PMID:25548905
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4356357/
Abstract

Human amnion epithelial cells (hAECs) derived from term or pre-term amnion membranes have attracted attention from researchers and clinicians as a potential source of cells for regenerative medicine. The reason for this interest is evidence that these cells have highly multipotent differentiation ability, low immunogenicity, and anti-inflammatory functions. These properties have prompted researchers to investigate the potential of hAECs to be used to treat a variety of diseases and disorders in pre-clinical animal studies with much success. hAECs have found widespread application for the treatment of a range of diseases and disorders. Potential clinical applications of hAECs include the treatment of stroke, multiple sclerosis, liver disease, diabetes and chronic and acute lung diseases. Progressing from pre-clinical animal studies into clinical trials requires a higher standard of quality control and safety for cell therapy products. For safety and quality control considerations, it is preferred that cell isolation protocols use animal product-free reagents. We have developed protocols to allow researchers to isolate, cryopreserve and culture hAECs using animal product-free reagents. The advantage of this method is that these cells can be isolated, characterized, cryopreserved and cultured without the risk of delivering potentially harmful animal pathogens to humans, while maintaining suitable cell yields, viabilities and growth potential. For researchers moving from pre-clinical animal studies to clinical trials, these methodologies will greatly accelerate regulatory approval, decrease risks and improve the quality of their therapeutic cell population.

摘要

源自足月或早产羊膜的人羊膜上皮细胞(hAECs)作为再生医学的潜在细胞来源,已引起研究人员和临床医生的关注。这种兴趣的原因是有证据表明这些细胞具有高度多能分化能力、低免疫原性和抗炎功能。这些特性促使研究人员在临床前动物研究中研究hAECs用于治疗各种疾病和病症的潜力,并取得了很大成功。hAECs已在治疗一系列疾病和病症中得到广泛应用。hAECs的潜在临床应用包括治疗中风、多发性硬化症、肝病、糖尿病以及慢性和急性肺病。从临床前动物研究进展到临床试验需要对细胞治疗产品有更高的质量控制和安全标准。出于安全和质量控制考虑,细胞分离方案最好使用无动物产品的试剂。我们已经开发出方案,使研究人员能够使用无动物产品的试剂分离、冷冻保存和培养hAECs。这种方法的优点是可以分离、鉴定、冷冻保存和培养这些细胞,而不会有将潜在有害的动物病原体传播给人类 的风险,同时保持合适的细胞产量、活力和生长潜力。对于从临床前动物研究转向临床试验 的研究人员来说,这些方法将大大加快监管审批,降低风险并提高其治疗细胞群体的质量。