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Pharmacologic fibroblast reprogramming into photoreceptors restores vision.药物诱导成纤维细胞重编程为光感受器可恢复视力。
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Glia-to-Neuron Conversion by CRISPR-CasRx Alleviates Symptoms of Neurological Disease in Mice.通过 CRISPR-CasRx 实现胶质细胞向神经元的转化可缓解小鼠神经疾病症状。
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Replacing what's lost: a new era of stem cell therapy for Parkinson's disease.替代所失之物:帕金森病干细胞治疗的新时代。
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Transcriptome-based molecular staging of human stem cell-derived retinal organoids uncovers accelerated photoreceptor differentiation by 9-cis retinal.基于转录组的人类干细胞衍生视网膜类器官分子分期揭示了9-顺式视黄醛加速光感受器分化。
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Patterning the Vertebrate Retina with Morphogenetic Signaling Pathways.用形态发生信号通路对脊椎动物视网膜进行模式化。
Neuroscientist. 2020 Apr;26(2):185-196. doi: 10.1177/1073858419874016. Epub 2019 Sep 11.
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Engineering universal cells that evade immune detection.工程通用细胞,逃避免疫检测。
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Using transcription factors for direct reprogramming of neurons .利用转录因子直接重编程神经元。
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8
Photoreceptor cell replacement in macular degeneration and retinitis pigmentosa: A pluripotent stem cell-based approach.黄斑变性和视网膜色素变性中的光感受器细胞替代:基于多能干细胞的方法。
Prog Retin Eye Res. 2019 Jul;71:1-25. doi: 10.1016/j.preteyeres.2019.03.001. Epub 2019 Mar 16.
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Concise Review: Update on Retinal Pigment Epithelium Transplantation for Age-Related Macular Degeneration.简明综述:年龄相关性黄斑变性的视网膜色素上皮移植更新。
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10
Chemical Conversion of Human Fetal Astrocytes into Neurons through Modulation of Multiple Signaling Pathways.通过调控多个信号通路将人胎儿星形胶质细胞化学转化为神经元。
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神经重编程用于组织修复和神经再生。

Neuronal Reprogramming for Tissue Repair and Neuroregeneration.

机构信息

Centre for Eye Research Australia, Royal Victorian Eye and Ear Hospital, Melbourne, VIC 3002, Australia.

Ophthalmology, Department of Surgery, University of Melbourne, Melbourne, VIC 3002, Australia.

出版信息

Int J Mol Sci. 2020 Jun 16;21(12):4273. doi: 10.3390/ijms21124273.

DOI:10.3390/ijms21124273
PMID:32560072
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7352898/
Abstract

Stem cell and cell reprogramming technology represent a rapidly growing field in regenerative medicine. A number of novel neural reprogramming methods have been established, using pluripotent stem cells (PSCs) or direct reprogramming, to efficiently derive specific neuronal cell types for therapeutic applications. Both in vitro and in vivo cellular reprogramming provide diverse therapeutic pathways for modeling neurological diseases and injury repair. In particular, the retina has emerged as a promising target for clinical application of regenerative medicine. Herein, we review the potential of neuronal reprogramming to develop regenerative strategy, with a particular focus on treating retinal degenerative diseases and discuss future directions and challenges in the field.

摘要

干细胞和细胞重编程技术代表了再生医学中一个快速发展的领域。已经建立了许多新的神经重编程方法,使用多能干细胞(PSCs)或直接重编程,以有效地衍生出特定的神经元细胞类型用于治疗应用。体外和体内细胞重编程为神经疾病和损伤修复的模型提供了多种治疗途径。特别是,视网膜已成为再生医学临床应用的一个很有前途的靶点。在此,我们综述了神经元重编程在开发再生策略方面的潜力,特别是在治疗视网膜退行性疾病方面,并讨论了该领域的未来方向和挑战。