Suppr超能文献

内视网膜的移植前景。

Transplantation prospects for the inner retina.

机构信息

Centre for Brain Repair, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.

出版信息

Eye (Lond). 2009 Oct;23(10):1980-4. doi: 10.1038/eye.2008.376. Epub 2008 Dec 19.

Abstract

Transplantation of stem or progenitor cells is an attractive new approach for treating neurodegenerative conditions of the central nervous system, which aims to protect or replace neurons and improve function. Proof of principle has already been shown in the retina that photoreceptors may be replaced by transplantation of neural progenitor cells. However, the task of retinal ganglion cell replacement is much more complex, as new cells will need to establish complex connections within the retina and also extend axons to precise targets in the brain. Although progress has been made in this field, it is likely that neuroprotective clinical applications will be established more quickly. Our laboratory has focused on the intraocular transplantation of cells to treat inner retinal disease, either by neuronal replacement or neuroprotection of existing cells. We have investigated the efficacy and effects of transplanting a variety of cell types, including human Müller stem cells (MIO-M1), oligodendrocyte precursor cells (OPCs), and bone marrow-derived mesenchymal stromal cells (MSCs) in a rat model of experimentally induced glaucoma. We also have developed and characterized a novel in vitro organotypic retinal explant culture system for exploring the methods of enhancing the efficacy of cell transplantation for the inner retina. In this review, we discuss the potentially beneficial effects of intraocular cell injections, identify current shortcomings of retinal stem cell therapy, and suggest directions for future research.

摘要

干细胞或祖细胞移植是一种治疗中枢神经系统神经退行性疾病的有吸引力的新方法,旨在保护或替代神经元并改善功能。在视网膜中已经证明了原理,即通过移植神经祖细胞可以替代光感受器。然而,视网膜神经节细胞替代的任务要复杂得多,因为新细胞需要在视网膜内建立复杂的连接,并将轴突延伸到大脑中的精确靶标。尽管在该领域已经取得了进展,但神经保护的临床应用可能会更快地建立。我们的实验室专注于通过细胞的眼内移植来治疗内视网膜疾病,无论是通过神经元替代还是对现有细胞的神经保护。我们已经研究了移植各种细胞类型的功效和影响,包括人 Müller 干细胞(MIO-M1)、少突胶质前体细胞(OPCs)和骨髓来源的间充质基质细胞(MSCs),以在实验性诱导性青光眼的大鼠模型中。我们还开发并表征了一种新型的体外器官型视网膜器官培养系统,用于探索增强内视网膜细胞移植功效的方法。在这篇综述中,我们讨论了眼内细胞注射的潜在有益效果,确定了视网膜干细胞治疗的当前不足之处,并提出了未来研究的方向。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验