氧化还原反应聚合物纳米凝胶作为秀丽隐杆线虫mRNA的高效递送载体。

microPublication biology Pub Date : 2024-12-10 eCollection Date: 2024-01-01 DOI:10.17912/micropub.biology.001428
Rupali Dabas, Alan Koh, David Carling, Nazila Kamaly, André E X Brown
{"title":"氧化还原反应聚合物纳米凝胶作为秀丽隐杆线虫mRNA的高效递送载体。","authors":"Rupali Dabas, Alan Koh, David Carling, Nazila Kamaly, André E X Brown","doi":"10.17912/micropub.biology.001428","DOIUrl":null,"url":null,"abstract":"<p><p>Efficient delivery of sensitive nucleic acid payloads, including mRNA, in <i>Caenorhabditis elegans</i> remains challenging, especially with traditional, labor-intensive transgenesis methods. We addressed these challenges using polymeric nanogels (NGs) as an advanced platform for mRNA delivery in <i>C. elegans</i> . These polymeric delivery vehicles can be engineered to suit desired applications owing to their chemical versatility, resulting from the ability to conjugate multiple functional groups onto the same backbone. Here, we validate the <i>in vivo</i> RNA delivery potential of redox-responsive NGs. The NGs showed up to 72.4 % RNA encapsulation and 6.61 % loading efficiencies and facilitated the controlled release of the mRNA payloads at intracellular concentrations of the reducing agent glutathione, where most of the RNA was released within 24 hours. As a proof of concept, we successfully delivered green fluorescent protein (GFP)-expressing mRNA using NGs in <i>C. elegans</i> for the first time. Physicochemical characterization revealed uniform NG size and charge, and fluorescence microscopy confirmed GFP expression in the gut after 24 hours of treatment. Our findings show NGs' potential as an mRNA delivery system in <i>C. elegans</i> .</p>","PeriodicalId":74192,"journal":{"name":"microPublication biology","volume":"2024 ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11669991/pdf/","citationCount":"0","resultStr":"{\"title\":\"Redox-Responsive Polymeric Nanogels as Efficient mRNA Delivery Vehicles in <i>Caenorhabditis elegans</i>.\",\"authors\":\"Rupali Dabas, Alan Koh, David Carling, Nazila Kamaly, André E X Brown\",\"doi\":\"10.17912/micropub.biology.001428\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Efficient delivery of sensitive nucleic acid payloads, including mRNA, in <i>Caenorhabditis elegans</i> remains challenging, especially with traditional, labor-intensive transgenesis methods. We addressed these challenges using polymeric nanogels (NGs) as an advanced platform for mRNA delivery in <i>C. elegans</i> . These polymeric delivery vehicles can be engineered to suit desired applications owing to their chemical versatility, resulting from the ability to conjugate multiple functional groups onto the same backbone. Here, we validate the <i>in vivo</i> RNA delivery potential of redox-responsive NGs. The NGs showed up to 72.4 % RNA encapsulation and 6.61 % loading efficiencies and facilitated the controlled release of the mRNA payloads at intracellular concentrations of the reducing agent glutathione, where most of the RNA was released within 24 hours. As a proof of concept, we successfully delivered green fluorescent protein (GFP)-expressing mRNA using NGs in <i>C. elegans</i> for the first time. Physicochemical characterization revealed uniform NG size and charge, and fluorescence microscopy confirmed GFP expression in the gut after 24 hours of treatment. Our findings show NGs' potential as an mRNA delivery system in <i>C. elegans</i> .</p>\",\"PeriodicalId\":74192,\"journal\":{\"name\":\"microPublication biology\",\"volume\":\"2024 \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-12-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11669991/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"microPublication biology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.17912/micropub.biology.001428\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"microPublication biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.17912/micropub.biology.001428","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

在秀丽隐杆线虫中有效地递送敏感的核酸有效载荷(包括mRNA)仍然具有挑战性,特别是传统的劳动密集型转基因方法。我们使用聚合物纳米凝胶(ng)作为秀丽隐杆线虫mRNA传递的先进平台来解决这些挑战。由于能够将多个官能团共轭到同一主链上,这些聚合物运载工具具有化学通用性,因此可以设计成适合所需的应用。在这里,我们验证了氧化还原反应性ng的体内RNA递送潜力。NGs显示出高达72.4%的RNA包封率和6.61%的装载效率,并促进了细胞内还原剂谷胱甘肽浓度下mRNA有效载荷的可控释放,其中大部分RNA在24小时内释放。作为概念验证,我们首次成功地使用NGs在秀丽隐杆线虫中传递了表达绿色荧光蛋白(GFP)的mRNA。理化表征显示NG大小和电荷均匀,荧光显微镜证实治疗24小时后肠道中有GFP表达。我们的研究结果表明,NGs在秀丽隐杆线虫中具有作为mRNA传递系统的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Redox-Responsive Polymeric Nanogels as Efficient mRNA Delivery Vehicles in Caenorhabditis elegans.

Efficient delivery of sensitive nucleic acid payloads, including mRNA, in Caenorhabditis elegans remains challenging, especially with traditional, labor-intensive transgenesis methods. We addressed these challenges using polymeric nanogels (NGs) as an advanced platform for mRNA delivery in C. elegans . These polymeric delivery vehicles can be engineered to suit desired applications owing to their chemical versatility, resulting from the ability to conjugate multiple functional groups onto the same backbone. Here, we validate the in vivo RNA delivery potential of redox-responsive NGs. The NGs showed up to 72.4 % RNA encapsulation and 6.61 % loading efficiencies and facilitated the controlled release of the mRNA payloads at intracellular concentrations of the reducing agent glutathione, where most of the RNA was released within 24 hours. As a proof of concept, we successfully delivered green fluorescent protein (GFP)-expressing mRNA using NGs in C. elegans for the first time. Physicochemical characterization revealed uniform NG size and charge, and fluorescence microscopy confirmed GFP expression in the gut after 24 hours of treatment. Our findings show NGs' potential as an mRNA delivery system in C. elegans .

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
审稿时长
3 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信