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用于视网膜疾病的间充质干细胞。

Mesenchymal stem cells for retinal diseases.

作者信息

Xu Wei, Xu Guo-Xing

机构信息

Fujian Institute of Ophthalmology, the First Affiliated Hospital of Fujian Medical University, Fuzhou 350005, Fujian Province, China.

出版信息

Int J Ophthalmol. 2011;4(4):413-21. doi: 10.3980/j.issn.2222-3959.2011.04.19. Epub 2011 Aug 18.

Abstract

Retinal diseases are featured with the common result of retinal cell apoptosis that will cause irreversible vision loss. Various attempts have been made for the solution against cell death. However, few approaches turn out to be effective. With the progress in mesenchymal stem cells (MSCs) research, MSCs were considered as a promising source for cell replacement or neuroprotection in retinal disorders. MSCs have the property of self-renewal and are multipotent cells derived from various mesenchymal tissues, which were demonstrated being capable of differentiating into multilineage tissue cells. Some works were also done to differentiate MSCs into retinal cells. MSCs could be induced to express retinal cell markers under certain stimuli. Recent studies also suggest that MSCs should be an ideal source for neuroprotection via the secretion of a variety of neurotrophins. Engineered MSCs were also used as vehicles for continuous delivery of neurotrophins against retinal degeneration with encouraging results. Since there are still barriers on the differentiation of MSCs into functional retinal cells, the use of MSCs for neuroprotection in retinal diseases seems to be a more practicable approach and worthy of further investigations.

摘要

视网膜疾病的共同特征是视网膜细胞凋亡,这将导致不可逆转的视力丧失。人们已经尝试了各种方法来解决细胞死亡问题。然而,很少有方法被证明是有效的。随着间充质干细胞(MSCs)研究的进展,MSCs被认为是视网膜疾病中细胞替代或神经保护的有希望的来源。MSCs具有自我更新的特性,是源自各种间充质组织的多能细胞,已证明能够分化为多谱系组织细胞。也有一些工作致力于将MSCs分化为视网膜细胞。在某些刺激下,MSCs可以被诱导表达视网膜细胞标志物。最近的研究还表明,MSCs通过分泌多种神经营养因子应该是神经保护的理想来源。工程化的MSCs也被用作持续递送神经营养因子以对抗视网膜变性的载体,结果令人鼓舞。由于MSCs分化为功能性视网膜细胞仍然存在障碍,因此在视网膜疾病中使用MSCs进行神经保护似乎是一种更可行的方法,值得进一步研究。

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Mesenchymal stem cells for retinal diseases.用于视网膜疾病的间充质干细胞。
Int J Ophthalmol. 2011;4(4):413-21. doi: 10.3980/j.issn.2222-3959.2011.04.19. Epub 2011 Aug 18.

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