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Mol Vis. 2019 Nov 11;25:663-678. eCollection 2019.
2
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3
Improved Retinal Organoid Differentiation by Modulating Signaling Pathways Revealed by Comparative Transcriptome Analyses with Development In Vivo.通过与体内发育的比较转录组分析揭示的信号通路调控,提高视网膜类器官的分化。
Stem Cell Reports. 2019 Nov 12;13(5):891-905. doi: 10.1016/j.stemcr.2019.09.009. Epub 2019 Oct 17.
4
Clinical-grade stem cell-derived retinal pigment epithelium patch rescues retinal degeneration in rodents and pigs.临床级别的干细胞衍生的视网膜色素上皮贴片可挽救啮齿动物和猪的视网膜变性。
Sci Transl Med. 2019 Jan 16;11(475). doi: 10.1126/scitranslmed.aat5580.
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Reproducibility of Molecular Phenotypes after Long-Term Differentiation to Human iPSC-Derived Neurons: A Multi-Site Omics Study.长期分化为人诱导多能干细胞源性神经元后的分子表型再现性:多中心组学研究。
Stem Cell Reports. 2018 Oct 9;11(4):897-911. doi: 10.1016/j.stemcr.2018.08.013. Epub 2018 Sep 20.
6
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Nutrients. 2018 Sep 1;10(9):1211. doi: 10.3390/nu10091211.
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9
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Invest Ophthalmol Vis Sci. 2018 Jun 1;59(7):2808-2817. doi: 10.1167/iovs.17-22069.
10
Regenerating Eye Tissues to Preserve and Restore Vision.再生眼部组织以保存和恢复视力。
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用于人诱导多能干细胞衍生的视网膜色素上皮均匀成熟的大豆蛋白纳米纤维支架。

Soy Protein Nanofiber Scaffolds for Uniform Maturation of Human Induced Pluripotent Stem Cell-Derived Retinal Pigment Epithelium.

机构信息

Neurobiology, Neurodegeneration and Repair Laboratory, National Eye Institute, National Institutes of Health, Bethesda, Maryland, USA.

Integrated Laboratory for Cellular Tissue Engineering and Regenerative Medicine, Department of Bioengineering, College of Engineering, Temple University, Philadelphia, Pennsylvania, USA.

出版信息

Tissue Eng Part C Methods. 2020 Aug;26(8):433-446. doi: 10.1089/ten.TEC.2020.0072.

DOI:10.1089/ten.TEC.2020.0072
PMID:32635833
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7462036/
Abstract

Retinal pigment epithelium (RPE) differentiated from human induced pluripotent stem cells, called induced retinal pigment epithelium (iRPE), is being explored as a cell-based therapy for the treatment of retinal degenerative diseases, especially age-related macular degeneration. The success of RPE implantation is linked to the use of biomimetic scaffolds that simulate Bruch's membrane and promote RPE maturation and integration as a functional tissue. Due to difficulties associated with animal protein-derived scaffolds, including sterility and pro-inflammatory responses, current practices favor the use of synthetic polymers, such as polycaprolactone (PCL), for generating nanofibrous scaffolds. In this study, we tested the hypothesis that plant protein-derived fibrous scaffolds can provide favorable conditions permissive for the maturation of RPE tissue sheets . Our natural, soy protein-derived nanofibrous scaffolds exhibited a J-shaped stress-strain curve that more closely resembled the mechanical properties of native tissues than PCL with significantly higher hydrophilicity of the natural scaffolds, favoring implantation. We then demonstrate that iRPE sheets growing on these soy protein scaffolds are equivalent to iRPE monolayers cultured on synthetic PCL nanofibrous scaffolds. Immunohistochemistry demonstrated RPE-like morphology and functionality with appropriate localization of RPE markers RPE65, PMEL17, Ezrin, and ZO1 and with anticipated histotypic polarization of vascular endothelial growth factor and pigment epithelium-derived growth factor as indicated by enzyme-linked immunosorbent assay. Scanning electron microscopy revealed dense microvilli on the cell surface and homogeneous tight junctional contacts between the cells. Finally, comparative transcriptome analysis in conjunction with principal component analysis demonstrated that iRPE on nanofibrous scaffolds, either natural or synthetic, matured more consistently than on nonfibrous substrates. Taken together, our studies suggest that the maturation of cultured iRPE sheets for subsequent clinical applications might benefit from the use of nanofibrous scaffolds generated from natural proteins. Impact statement Induced retinal pigment epithelium (iRPE) from patient-derived induced pluripotent stem cells (iPSCs) may yield powerful treatments of retinal diseases, including age-related macular degeneration. Recent studies, including early human clinical trials, demonstrate the importance of selecting appropriate biomaterial scaffolds to support tissue-engineered iRPE sheets during implantation. Electrospun scaffolds show particular promise due to their similarity to the structure of the native Bruch's membrane. In this study, we describe the use of electroprocessed nanofibrous soy protein scaffolds to generate polarized sheets of human iPSC-derived iRPE sheets. Our evaluation, including RNA-seq transcriptomics, indicates that these scaffolds are viable alternatives to scaffolds electrospun from synthetic polymers.

摘要

视网膜色素上皮(RPE)由人诱导多能干细胞分化而来,称为诱导视网膜色素上皮(iRPE),目前正在作为细胞疗法探索用于治疗视网膜退行性疾病,尤其是年龄相关性黄斑变性。RPE 移植的成功与仿生支架的使用有关,这些支架模拟布鲁赫膜并促进 RPE 成熟和整合为功能性组织。由于动物蛋白衍生支架存在与无菌和促炎反应相关的困难,目前的实践倾向于使用合成聚合物,如聚己内酯(PCL),来生成纳米纤维支架。在这项研究中,我们检验了这样一个假设,即植物蛋白衍生的纤维支架可以为 RPE 组织片的成熟提供有利条件。我们的天然、大豆蛋白衍生的纳米纤维支架表现出 J 形的应力-应变曲线,更接近天然组织的机械性能,而 PCL 具有明显更高的亲水性,有利于植入。然后,我们证明在这些大豆蛋白支架上生长的 iRPE 片与在合成 PCL 纳米纤维支架上培养的 iRPE 单层相当。免疫组织化学显示 RPE 样形态和功能,适当定位 RPE 标志物 RPE65、PMEL17、Ezrin 和 ZO1,并通过酶联免疫吸附试验预期表现出血管内皮生长因子和色素上皮衍生生长因子的组织型极化。扫描电子显微镜显示细胞表面有密集的微绒毛,细胞之间有均匀的紧密连接。最后,结合主成分分析的比较转录组分析表明,在天然或合成纳米纤维支架上培养的 iRPE 比在非纤维基质上更一致地成熟。总之,我们的研究表明,用于后续临床应用的培养 iRPE 片的成熟可能受益于使用天然蛋白生成的纳米纤维支架。