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胚胎干细胞与蛋白质诱导多能干细胞多巴胺能神经元分化效率的比较研究。

Comparative study of efficacy of dopaminergic neuron differentiation between embryonic stem cell and protein-based induced pluripotent stem cell.

作者信息

Kwon Yoo-Wook, Chung Yeon-Ju, Kim Joonoh, Lee Ho-Jae, Park Jihwan, Roh Tae-Young, Cho Hyun-Jai, Yoon Chang-Hwan, Koo Bon-Kwon, Kim Hyo-Soo

机构信息

National Research Laboratory for Stem Cell Niche, Seoul National University Hospital, Seoul, Korea ; Innovative Research Institute for Cell Therapy, Seoul National University Hospital, Seoul, Korea.

Division of Molecular and Life Sciences,Pohang University of Science and Technology, Pohang, Korea.

出版信息

PLoS One. 2014 Jan 22;9(1):e85736. doi: 10.1371/journal.pone.0085736. eCollection 2014.

Abstract

In patients with Parkinson's disease (PD), stem cells can serve as therapeutic agents to restore or regenerate injured nervous system. Here, we differentiated two types of stem cells; mouse embryonic stem cells (mESCs) and protein-based iPS cells (P-iPSCs) generated by non-viral methods, into midbrain dopaminergic (mDA) neurons, and then compared the efficiency of DA neuron differentiation from these two cell types. In the undifferentiated stage, P-iPSCs expressed pluripotency markers as ES cells did, indicating that protein-based reprogramming was stable and authentic. While both stem cell types were differentiated to the terminally-matured mDA neurons, P-iPSCs showed higher DA neuron-specific markers' expression than ES cells. To investigate the mechanism of the superior induction capacity of DA neurons observed in P-iPSCs compared to ES cells, we analyzed histone modifications by genome-wide ChIP sequencing analysis and their corresponding microarray results between two cell types. We found that Wnt signaling was up-regulated, while SFRP1, a counter-acting molecule of Wnt, was more suppressed in P-iPSCs than in mESCs. In PD rat model, transplantation of neural precursor cells derived from both cell types showed improved function. The present study demonstrates that P-iPSCs could be a suitable cell source to provide patient-specific therapy for PD without ethical problems or rejection issues.

摘要

在帕金森病(PD)患者中,干细胞可作为治疗剂来恢复或再生受损的神经系统。在此,我们将两种类型的干细胞,即小鼠胚胎干细胞(mESCs)和通过非病毒方法产生的基于蛋白质的诱导多能干细胞(P-iPSCs),分化为中脑多巴胺能(mDA)神经元,然后比较这两种细胞类型向DA神经元分化的效率。在未分化阶段,P-iPSCs与ES细胞一样表达多能性标志物,表明基于蛋白质的重编程是稳定且真实的。虽然两种干细胞类型都分化为终末成熟的mDA神经元,但P-iPSCs显示出比ES细胞更高的DA神经元特异性标志物表达。为了研究与ES细胞相比,在P-iPSCs中观察到的对DA神经元的优越诱导能力的机制,我们通过全基因组ChIP测序分析及其在两种细胞类型之间的相应微阵列结果分析了组蛋白修饰。我们发现Wnt信号通路在P-iPSCs中上调,而Wnt的拮抗分子SFRP1在P-iPSCs中比在mESCs中受到更强烈的抑制。在PD大鼠模型中,移植源自这两种细胞类型的神经前体细胞显示出功能改善。本研究表明,P-iPSCs可能是一种合适的细胞来源,可为PD提供针对患者的治疗,而不存在伦理问题或排斥问题。

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