四面体框架核酸和 tFNAs-miR22 对视网膜缺血再灌注损伤的治疗作用

IF 5.9 1区 生物学 Q2 CELL BIOLOGY Cell Proliferation Pub Date : 2024-07-31 DOI:10.1111/cpr.13695
Xiaoxiao Xu, Yanyan Fu, Delun Luo, Lina Zhang, Xi Huang, Yingying Chen, Chunyan Lei, Jinnan Liu, Shiqi Li, Zhouyuan Yu, Yunfeng Lin, Meixia Zhang
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引用次数: 0

摘要

视网膜缺血/再灌注损伤(RI/R)是眼科疾病中常见的病理过程,可导致严重的视力损伤。RI/R损伤和修复的机制尚不清楚。学者们正在积极探索有效的干预策略,以恢复受损的视觉功能。随着核酸纳米材料的发展,四面体框架核酸(tFNAs)因其优异的生物特性,在干细胞、生物传感器和肿瘤治疗等多个领域显示出良好的治疗潜力。此外,miRNA-22-3p(miR-22)作为神经组织中的重要调控因子,已被证实对多种神经退行性疾病有积极作用。通过稳定构建四面体框架核酸 miR22 复合物(tFNAs-miR22),我们观察到 tFNAs-miR22 对视网膜神经组织 RI/R 损伤的修复有积极作用。先前的研究表明,tFNAs 能有效地将 miR-22 运送到受损的视网膜神经元中,从而发挥神经保护作用。有趣的是,我们发现 tFNAs 和 miR-22 之间存在一定的协同作用。tFNAs-miR22 可选择性地激活 ERK1/2 信号通路,从而减少神经元凋亡,加速细胞增殖,恢复突触功能活性。在这项研究中,我们建立了一种简单而有效的治疗 RI/R 的小分子药物,它可能成为未来治疗这类视力损伤疾病的一种有前途的神经保护剂。
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Therapeutic effects of tetrahedral framework nucleic acids and tFNAs-miR22 on retinal ischemia/reperfusion injury

Retinal ischemia/reperfusion injury (RI/R) is a common pathological process in ophthalmic diseases, which can cause severe visual impairment. The mechanisms underlying RI/R damage and repair are still unclear. Scholars are actively exploring effective intervention strategies to restore impaired visual function. With the development of nucleic acid nanomaterials, tetrahedral framework nucleic acids (tFNAs) have shown promising therapeutic potential in various fields such as stem cells, biosensors, and tumour treatment due to their excellent biological properties. Besides, miRNA-22-3p (miR-22), as an important regulatory factor in neural tissue, has been proven to have positive effects in various neurodegenerative diseases. By stably constructing a complex of tetrahedral framework nucleic acids miR22 (tFNAs-miR22), we observed that tFNAs-miR22 had a positive effect on the repair of RI/R injury in retinal neural tissue. Previous studies have shown that tFNAs can effectively deliver miR-22 into damaged retinal neurons, subsequently exerting neuroprotective effects. Interestingly, we found that there was a certain synergistic effect between tFNAs and miR-22. tFNAs-miR22 can selectively activated the ERK1/2 signalling pathway to reduce neuronal apoptosis, accelerate cell proliferation, and restore synaptic functional activity. In this study, we established a simple yet effective small molecule drug for RI/R treatment which may become a promising neuroprotectant for treating this type of vision impairment disease in the future.

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来源期刊
Cell Proliferation
Cell Proliferation 生物-细胞生物学
CiteScore
14.80
自引率
2.40%
发文量
198
审稿时长
1 months
期刊介绍: Cell Proliferation Focus: Devoted to studies into all aspects of cell proliferation and differentiation. Covers normal and abnormal states. Explores control systems and mechanisms at various levels: inter- and intracellular, molecular, and genetic. Investigates modification by and interactions with chemical and physical agents. Includes mathematical modeling and the development of new techniques. Publication Content: Original research papers Invited review articles Book reviews Letters commenting on previously published papers and/or topics of general interest By organizing the information in this manner, readers can quickly grasp the scope, focus, and publication content of Cell Proliferation.
期刊最新文献
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