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2
Pharmacological Modulation of Photoreceptor Outer Segment Degradation in a Human iPS Cell Model of Inherited Macular Degeneration.遗传性黄斑变性人诱导多能干细胞模型中光感受器外段降解的药理学调控
Mol Ther. 2015 Nov;23(11):1700-1711. doi: 10.1038/mt.2015.141. Epub 2015 Aug 24.
3
Stem cell based therapies for age-related macular degeneration: The promises and the challenges.基于干细胞的治疗方法治疗年龄相关性黄斑变性:承诺与挑战。
Prog Retin Eye Res. 2015 Sep;48:1-39. doi: 10.1016/j.preteyeres.2015.06.004. Epub 2015 Jun 23.
4
Using Stem Cells to Model Diseases of the Outer Retina.利用干细胞构建视网膜外层疾病模型。
Comput Struct Biotechnol J. 2015 May 6;13:382-9. doi: 10.1016/j.csbj.2015.05.001. eCollection 2015.
5
Chromosome microduplication in somatic cells decreases the genetic stability of human reprogrammed somatic cells and results in pluripotent stem cells.体细胞中的染色体微重复会降低人类重编程体细胞的遗传稳定性,并产生多能干细胞。
Sci Rep. 2015 May 12;5:10114. doi: 10.1038/srep10114.
6
Preferential gene expression and epigenetic memory of induced pluripotent stem cells derived from mouse pancreas.诱导多能干细胞来源于小鼠胰腺的基因表达偏爱和表观遗传记忆。
Genes Cells. 2015 May;20(5):367-81. doi: 10.1111/gtc.12227. Epub 2015 Feb 27.
7
Generation of highly enriched populations of optic vesicle-like retinal cells from human pluripotent stem cells.从人多能干细胞中生成高度富集的视泡样视网膜细胞群体。
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The generation of induced pluripotent stem cells for macular degeneration as a drug screening platform: identification of curcumin as a protective agent for retinal pigment epithelial cells against oxidative stress.将诱导多能干细胞用于黄斑变性的药物筛选平台:鉴定姜黄素作为一种保护性物质,用于抵抗视网膜色素上皮细胞的氧化应激。
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10
The use of induced pluripotent stem cells to reveal pathogenic gene mutations and explore treatments for retinitis pigmentosa.利用诱导多能干细胞揭示致病基因突变并探索视网膜色素变性的治疗方法。
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诱导多能干细胞与外层视网膜疾病

Induced Pluripotent Stem Cells and Outer Retinal Disease.

作者信息

Yang Jin, Cai Bingcui, Glencer Patrick, Li Zhiqing, Zhang Xiaomin, Li Xiaorong

机构信息

Tianjin Medical University Eye Hospital, Tianjin 300384, China.

Nova Southeastern College of Optometry, Fort Lauderdale, FL 33314, USA.

出版信息

Stem Cells Int. 2016;2016:2850873. doi: 10.1155/2016/2850873. Epub 2016 Jan 5.

DOI:10.1155/2016/2850873
PMID:26880948
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4736410/
Abstract

The retina, which is composed of multiple layers of differing cell types, has been considered the first choice for gene therapy, disease modeling, and stem cell-derived retinal cell transplant therapy. Because of its special characteristics, the retina, located in the posterior part of the eye, can be well observed directly after gene therapy or transplantation. The blood-retinal barrier is part of a specialized ocular microenvironment that is immune privileged. This protects transplanted cells and tissue. Having two eyes makes perfect natural control possible after a single eye receives gene or stem cell therapy. For this reason, research about exploring retinal diseases' underlying molecular mechanisms and potential therapeutic approach using stem cell technique has been developing rapidly. This review is to present an up-to-date summary of the iPSC's sources, variations, differentiation methods, and the wide-ranging application of iPSCs-RPCS or iPSCs-RPE on retinal disease modeling, diagnostics, and therapeutics.

摘要

视网膜由多层不同类型的细胞组成,一直被视为基因治疗、疾病建模和干细胞衍生视网膜细胞移植治疗的首选。由于其特殊特性,位于眼球后部的视网膜在基因治疗或移植后可直接被很好地观察到。血视网膜屏障是免疫特权的特殊眼部微环境的一部分。这保护了移植的细胞和组织。拥有双眼使得在单眼接受基因或干细胞治疗后进行完美的自然对照成为可能。因此,利用干细胞技术探索视网膜疾病潜在分子机制和潜在治疗方法的研究发展迅速。本综述旨在对诱导多能干细胞(iPSC)的来源、变体、分化方法以及iPSC来源的视网膜色素上皮细胞(iPSCs-RPE)或iPSC来源的视网膜祖细胞(iPSCs-RPC)在视网膜疾病建模、诊断和治疗方面的广泛应用进行最新总结。