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Otx2 增强 Müller 细胞来源的视网膜干细胞向光感受器样细胞的转分化。

Otx2 enhances transdifferentiation of Müller cells-derived retinal stem cells into photoreceptor-like cells.

机构信息

Department of Ophthalmology, Xiangya Hospital, Central South University, Changsha, China.

Department of Ophthalmology, The Second Affiliated Hospital of Nanchang University, Nanchang, China.

出版信息

J Cell Mol Med. 2019 Feb;23(2):943-953. doi: 10.1111/jcmm.13995. Epub 2018 Nov 19.

Abstract

Retinal Müller glial cells have the potential of neurogenic retinal progenitor cells, and could reprogram into retinal-specific cell types such as photoreceptor cells. How to promote the differentiation of Müller cells into photoreceptor cells represents a promising therapy strategy for retinal degeneration diseases. This study aimed to enhance the transdifferentiation of rat Müller cells-derived retinal stem cells (MC-RSCs) into photoreceptor-like cells and explore the signalling mechanism. We dedifferentiated rat Müller cells into MC-RSCs which were infected with Otx2 overexpression lentivirus or control. The positive rate of photoreceptor-like cells among MC-RSCs treated with Otx2 overexpression lentivirus was significantly higher compared to control. Furthermore, pre-treatment with Crx siRNA, Nrl siRNA, or GSK-3 inhibitor SB-216763 reduced the positive rate of photoreceptor-like cells among MC-RSCs treated with Otx2 overexpression lentivirus. Finally, Otx2 induced photoreceptor precursor cells were injected into subretinal space of N-methyl-N-nitrosourea induced rat model of retinal degeneration and partially recovered retinal degeneration in the rats. In conclusion, Otx2 enhances transdifferentiation of MC-RSCs into photoreceptor-like cells and this is associated with the inhibition of Wnt signalling. Otx2 is a potential target for gene therapy of retinal degenerative diseases.

摘要

视网膜 Müller 胶质细胞具有神经源性视网膜祖细胞的潜能,并且可以重编程为视网膜特异性细胞类型,如光感受器细胞。如何促进 Müller 细胞向光感受器细胞分化代表了治疗视网膜变性疾病的一种很有前途的治疗策略。本研究旨在增强大鼠 Müller 细胞源性视网膜干细胞(MC-RSCs)向光感受器样细胞的转分化,并探讨其信号机制。我们将大鼠 Müller 细胞去分化为 MC-RSCs,然后用过表达 Otx2 的慢病毒或对照物感染。与对照组相比,用过表达 Otx2 的慢病毒处理的 MC-RSCs 中转分化为光感受器样细胞的阳性率明显更高。此外,Crx siRNA、Nrl siRNA 或 GSK-3 抑制剂 SB-216763 的预处理降低了 Otx2 过表达慢病毒处理的 MC-RSCs 中转分化为光感受器样细胞的阳性率。最后,将 Otx2 诱导的光感受器前体细胞注入 N-甲基-N-亚硝脲诱导的大鼠视网膜变性模型的视网膜下腔,部分恢复了大鼠的视网膜变性。总之,Otx2 增强了 MC-RSCs 向光感受器样细胞的转分化,这与 Wnt 信号通路的抑制有关。Otx2 是视网膜退行性疾病基因治疗的一个潜在靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/676f/6349218/0f61b0d25585/JCMM-23-943-g001.jpg

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