Suppr超能文献

四面体核酸框架和 tFNAs-miR22 对视网膜缺血/再灌注损伤的治疗作用。

Therapeutic effects of tetrahedral framework nucleic acids and tFNAs-miR22 on retinal ischemia/reperfusion injury.

机构信息

Department of Ophthalmology, and Research Laboratory of Macular Disease, West China Hospital, Sichuan University, Chengdu, China.

Innovative Institute of Chinese Medicine and Pharmacy, Chengdu University of Traditional Chinese Medicine, Chengdu, China.

出版信息

Cell Prolif. 2024 Nov;57(11):e13695. doi: 10.1111/cpr.13695. Epub 2024 Jul 31.

Abstract

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.

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害。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)由于其优异的生物学特性,在干细胞、生物传感器和肿瘤治疗等领域显示出有前途的治疗潜力。此外,miR-22-3p(miR-22)作为神经组织中的重要调节因子,已被证明在各种神经退行性疾病中具有积极作用。通过稳定构建四面体框架核酸 miR22(tFNAs-miR22)复合物,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 可以有效地将 miR-22 递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 可以选择性地激活 ERK1/2 信号通路,减少神经元凋亡,促进细胞增殖,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小分子药物治疗 RI/R,它可能成为未来治疗这种视力损害疾病的有前途的神经保护剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f98/11533083/69cf410ce44c/CPR-57-e13695-g004.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验