Kexuan Zou, Pengfei Zhang, Yuqi Wang, Yan Liu, Bin Ji, Pengfei Zhan, Jie Song
{"title":"Investigation and Regulation of DNA Nanostructures on Activating cGAS-STING Signaling.","authors":"Kexuan Zou, Pengfei Zhang, Yuqi Wang, Yan Liu, Bin Ji, Pengfei Zhan, Jie Song","doi":"10.1002/smtd.202401041","DOIUrl":null,"url":null,"abstract":"<p><p>DNA nanostructures have shown great potential in biomedical fields. However, the immune responses, especially the activation of the cGAS-STING signaling (A-cGSs), induced by DNA nanostructures, remain incompletely understood. Here, the ability of various DNA nanostructures from double-stranded DNA (dsDNA), single-stranded tiles (SSTs) to DNA origami is investigated on A-cGSs. Unlike natural dsDNA which triggers potent A-cGSs, the structural interconnectivity of various DNA configurations can substantially reduce the occurrence of A-cGSs, irrespective of their form, dimensions, and conformation. However, wireframe DNA nanostructures can activate the cGAS-STING signaling, suggesting that decreasing A-cGSs is dsDNA compactness-dependent. Based on this, a reconfigurable DNA Origami Domino Array (DODA) is used to systematically interrogate how dsDNA influences the A-cGSs and demonstrates that the length, number, and space of dsDNA array coordinately influence the activation level of cGAS-STING signaling, realizing a regulation of innate immune response. The above data and findings enhance the understanding of how DNA nanostructures affect cellular innate immune responses and new insights into the modulation of innate immune responses by DNA nanomedicine.</p>","PeriodicalId":229,"journal":{"name":"Small Methods","volume":null,"pages":null},"PeriodicalIF":10.7000,"publicationDate":"2024-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Small Methods","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/smtd.202401041","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
DNA nanostructures have shown great potential in biomedical fields. However, the immune responses, especially the activation of the cGAS-STING signaling (A-cGSs), induced by DNA nanostructures, remain incompletely understood. Here, the ability of various DNA nanostructures from double-stranded DNA (dsDNA), single-stranded tiles (SSTs) to DNA origami is investigated on A-cGSs. Unlike natural dsDNA which triggers potent A-cGSs, the structural interconnectivity of various DNA configurations can substantially reduce the occurrence of A-cGSs, irrespective of their form, dimensions, and conformation. However, wireframe DNA nanostructures can activate the cGAS-STING signaling, suggesting that decreasing A-cGSs is dsDNA compactness-dependent. Based on this, a reconfigurable DNA Origami Domino Array (DODA) is used to systematically interrogate how dsDNA influences the A-cGSs and demonstrates that the length, number, and space of dsDNA array coordinately influence the activation level of cGAS-STING signaling, realizing a regulation of innate immune response. The above data and findings enhance the understanding of how DNA nanostructures affect cellular innate immune responses and new insights into the modulation of innate immune responses by DNA nanomedicine.
DNA 纳米结构在生物医学领域显示出巨大潜力。然而,人们对 DNA 纳米结构诱导的免疫反应,尤其是 cGAS-STING 信号(A-cGSs)的激活仍不甚了解。在此,我们研究了从双链DNA(dsDNA)、单链瓦片(SST)到DNA折纸等各种DNA纳米结构对A-cGSs的能力。与天然dsDNA引发强烈的A-cGSs不同,各种DNA构型的结构互联性可以大大减少A-cGSs的发生,无论其形式、尺寸和构象如何。然而,线框DNA纳米结构可以激活cGAS-STING信号,这表明A-cGS的减少与dsDNA的紧凑程度有关。在此基础上,研究人员利用可重构的DNA折纸多米诺阵列(DODA)系统地研究了dsDNA如何影响A-cGSs,结果表明dsDNA阵列的长度、数量和空间协调地影响了cGAS-STING信号的激活水平,实现了对先天性免疫反应的调控。上述数据和发现加深了人们对DNA纳米结构如何影响细胞先天性免疫反应的理解,为DNA纳米药物调控先天性免疫反应提供了新的见解。
Small MethodsMaterials Science-General Materials Science
CiteScore
17.40
自引率
1.60%
发文量
347
期刊介绍:
Small Methods is a multidisciplinary journal that publishes groundbreaking research on methods relevant to nano- and microscale research. It welcomes contributions from the fields of materials science, biomedical science, chemistry, and physics, showcasing the latest advancements in experimental techniques.
With a notable 2022 Impact Factor of 12.4 (Journal Citation Reports, Clarivate Analytics, 2023), Small Methods is recognized for its significant impact on the scientific community.
The online ISSN for Small Methods is 2366-9608.