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选择性表达的RNA分子作为功能化细胞靶向的通用工具。

Selectively expressed RNA molecules as a versatile tool for functionalized cell targeting.

作者信息

Rastfeld Frederik, Hoffmann Marco, Krüger Sylvie, Bohn Patrick, Gribling-Burrer Anne-Sophie, Wagner Laura, Hersch Nils, Stegmayr Carina, Lövenich Lukas, Gerlach Sven, Köninger Daniel, Hoffmann Christina, Walter Helene L, Wiedermann Dirk, Manoharan Hajaani, Fink Gereon R, Merkel Rudolf, Bohlen Heribert, Smyth Redmond P, Rueger Maria A, Hoffmann Bernd

机构信息

Institute of Biological Information Processing, IBI-2: Mechanobiology, Research Centre Juelich, Juelich, Germany.

Helmholtz Institute for RNA-based Infection Research, Helmholtz Centre for Infection Research, Würzburg, Germany.

出版信息

Nat Commun. 2025 Jan 6;16(1):420. doi: 10.1038/s41467-024-55547-6.

DOI:10.1038/s41467-024-55547-6
PMID:39762287
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11704337/
Abstract

Targeting of diseased cells is one of the most urgently needed prerequisites for a next generation of potent pharmaceuticals. Different approaches pursued fail mainly due to a lack of specific surface markers. Developing an RNA-based methodology, we can now ensure precise cell targeting combined with selective expression of effector proteins for therapy, diagnostics or cell steering. The specific combination of the molecular properties of antisense technology and mRNA therapy with functional RNA secondary structures allowed us to develop selectively expressed RNA molecules for medical applications. These seRNAs remain inactive in non-target cells and induce translation by partial degradation only in preselected cell types of interest. Cell specificity and type of functionalization are easily adaptable based on a modular system. In proof-of-concept studies we use seRNAs as platform technology for highly selective cell targeting. We effectively treat breast tumor cell clusters in mixed cell systems and shrink early U87 glioblastoma cell clusters in the brain of male mice without detectable side effects. Our data open up potential avenues for various therapeutic applications.

摘要

靶向病变细胞是新一代强效药物最迫切需要的先决条件之一。目前所采用的不同方法大多因缺乏特异性表面标志物而失败。通过开发一种基于RNA的方法,我们现在可以确保精确的细胞靶向,同时结合效应蛋白的选择性表达用于治疗、诊断或细胞操控。反义技术和mRNA疗法的分子特性与功能性RNA二级结构的特定组合,使我们能够开发出用于医学应用的选择性表达RNA分子。这些选择性表达的RNA(seRNAs)在非靶细胞中保持无活性,并且仅在预先选定的目标细胞类型中通过部分降解诱导翻译。基于模块化系统,细胞特异性和功能化类型很容易调整。在概念验证研究中,我们将seRNAs用作高度选择性细胞靶向的平台技术。我们有效地治疗了混合细胞系统中的乳腺肿瘤细胞簇,并缩小了雄性小鼠大脑中早期U87胶质母细胞瘤细胞簇,且未检测到副作用。我们的数据为各种治疗应用开辟了潜在途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4224/11704337/4ac835736101/41467_2024_55547_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4224/11704337/58a4cf2807f5/41467_2024_55547_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4224/11704337/b49f2fb4dead/41467_2024_55547_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4224/11704337/913467f636f8/41467_2024_55547_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4224/11704337/7644f7fae609/41467_2024_55547_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4224/11704337/9edb7dbf1170/41467_2024_55547_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4224/11704337/bcb7aa5df541/41467_2024_55547_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4224/11704337/4ac835736101/41467_2024_55547_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4224/11704337/58a4cf2807f5/41467_2024_55547_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4224/11704337/b49f2fb4dead/41467_2024_55547_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4224/11704337/913467f636f8/41467_2024_55547_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4224/11704337/7644f7fae609/41467_2024_55547_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4224/11704337/9edb7dbf1170/41467_2024_55547_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4224/11704337/bcb7aa5df541/41467_2024_55547_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4224/11704337/4ac835736101/41467_2024_55547_Fig7_HTML.jpg

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本文引用的文献

1
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Nat Protoc. 2024 Jun;19(6):1835-1865. doi: 10.1038/s41596-024-00959-3. Epub 2024 Feb 12.
2
Preclinical Models and Technologies in Glioblastoma Research: Evolution, Current State, and Future Avenues.神经胶质瘤研究中的临床前模型和技术:发展、现状和未来方向。
Int J Mol Sci. 2023 Nov 14;24(22):16316. doi: 10.3390/ijms242216316.
3
Nano-DMS-MaP allows isoform-specific RNA structure determination.纳米 DMS-MaP 可实现异构体特异性 RNA 结构测定。
Nat Methods. 2023 Jun;20(6):849-859. doi: 10.1038/s41592-023-01862-7. Epub 2023 Apr 27.
4
PEGylation and folic-acid functionalization of cationic lipoplexes-Improved nucleic acid transfer into cancer cells.阳离子脂质体的聚乙二醇化和叶酸功能化——提高核酸向癌细胞的转染效率
Front Bioeng Biotechnol. 2022 Dec 21;10:1066887. doi: 10.3389/fbioe.2022.1066887. eCollection 2022.
5
Preparation of selective organ-targeting (SORT) lipid nanoparticles (LNPs) using multiple technical methods for tissue-specific mRNA delivery.采用多种技术方法制备具有组织特异性的 mRNA 递药的选择性器官靶向(SORT)脂质纳米粒(LNPs)。
Nat Protoc. 2023 Jan;18(1):265-291. doi: 10.1038/s41596-022-00755-x. Epub 2022 Oct 31.
6
Programmable RNA sensing for cell monitoring and manipulation.可编程 RNA 传感用于细胞监测和操作。
Nature. 2022 Oct;610(7933):713-721. doi: 10.1038/s41586-022-05280-1. Epub 2022 Oct 5.
7
Modular, programmable RNA sensing using ADAR editing in living cells.利用 ADAR 编辑在活细胞中进行模块化、可编程的 RNA 感应。
Nat Biotechnol. 2023 Apr;41(4):482-487. doi: 10.1038/s41587-022-01493-x. Epub 2022 Oct 5.
8
Differential bicistronic gene translation mediated by the internal ribosome entry site element of encephalomyocarditis virus.脑炎心肌炎病毒内部核糖体进入位点元件介导的差异双顺反子基因翻译。
Biomed J. 2021 Dec;44(6 Suppl 1):S54-S62. doi: 10.1016/j.bj.2020.06.006. Epub 2020 Jun 24.
9
On the mechanism of tissue-specific mRNA delivery by selective organ targeting nanoparticles.选择性靶向器官纳米颗粒介导组织特异性 mRNA 递送的机制研究。
Proc Natl Acad Sci U S A. 2021 Dec 28;118(52). doi: 10.1073/pnas.2109256118.
10
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Nat Biotechnol. 2022 Apr;40(4):539-545. doi: 10.1038/s41587-021-01068-2. Epub 2021 Oct 28.