医学
间充质干细胞
血管生成
神经保护
视神经病变
微泡
干细胞
外体
视神经炎
生物信息学
干细胞疗法
再生(生物学)
免疫学
病理
眼科
视神经
药理学
多发性硬化
癌症研究
生物
小RNA
细胞生物学
基因
生物化学
作者
Dongli Li,Yuanyuan Gong
出处
期刊:Current stem cell research & therapy
[Bentham Science]
日期:2021-02-12
卷期号:16 (2): 109-114
被引量:4
标识
DOI:10.2174/1574888x15666200814121849
摘要
Non-arteritic anterior ischemic optic neuropathy (NAION) is a leading cause of optic nerverelated permanent visual impairment among individuals of over 50 years of age after glaucoma. Due to perplexing disorder regarding its pathogenesis, there is still no widely accepted and established treatment plan. Mesenchymal stem cells (MSCs) are one of the rare stem cell types that therapeutic agents for immunomodulation and ischemic tissue repair in clinical practice. However, there are certain disadvantages in using MSCs, such as potential tumorigenicity, need for autologous collection, and short survival time. Previous evidence suggested that MSC-exosome significantly attenuated post-ischemic neuronal damage and induced long-term neuroprotection associated with enhanced angiogenesis in MSCs. Therefore, we hypothesized that the intravitreal administration of MSC-exosome could be a potentially effective therapeutic approach for NAION by using a similar mechanism via promoting angiogenesis, neuro-regeneration, and neurological recovery, suppressing oxidative stress and reducing apoptosis, and suppressing inflammation and immunity based on its biological structure and function in NAION. Questions that need to be answered before testing clinically include dose regimen, injection frequency, the optimal duration of treatment, and duration of medication.
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