移植干细胞前体减少青光眼神经退行性变

H. Tariq, A. Tariq, Uzma Yasmeen
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引用次数: 0

摘要

青光眼是一种常见的神经退行性疾病,目前的治疗方法往往不足。我们研究的目的是确定少突胶质前体细胞(OPCs),一种神经干细胞,是否可以保护视网膜神经节细胞(RGCs)免受青光眼损伤。方法:单侧对成年大鼠眼进行小梁激光治疗,慢性升高眼压。在体外分离OPCs,然后在损伤诱导前或与损伤诱导同时在玻璃体内移植。结果:移植的OPCs在眼内存活至少12周,且定位于rgc附近。此外,OPCs显著提高青光眼RGCs的存活,但仅在炎症同时激活的情况下。RGC死亡的改善不归因于炎症,而是依赖于炎症细胞和OPCs之间的相互作用。移植细胞在体内也表现出多能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reduction of Neuro degeneration in Glaucoma by Transplanted stems Cells Precursors
Introduction: Glaucoma is a common neurodegenerative disease for which current therapies are often insufficient. The purpose of our investigation was to determine whether Oligodendrocyte Precursor Cells (OPCs), a type of neural stem cell, can protect Retinal Ganglion Cells (RGCs) from glaucomatous damage in vivo. Methods: Intraocular pressure was chronically increased by trabecular laser treatment delivered unilaterally to adult rat eyes. OPCs were isolated in vitro and then transplanted intra vitreally either before, or concurrent with, injury induction. Results: Transplanted OPCs were found to survive within the eye for at least 12 weeks and to localize close to the RGCs. Moreover, OPCs significantly enhanced the survival of RGCs in the glaucomatous eye, but only when concomitantly activated by inflammation.. Amelioration of RGC death was not attributable to inflammation but relied on an interaction between inflammatory cells and OPCs. Engrafted cells also displayed multipotentiality in vivo.
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