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再生医学中的组织纳米转染与细胞重编程以及抗菌动力学

Tissue nanotransfection and cellular reprogramming in regenerative medicine and antimicrobial dynamics.

作者信息

Shakra Mohammed Youssef

机构信息

Damietta Faculty of Medicine, Al-Azhar University, Damietta, Egypt.

出版信息

Front Bioeng Biotechnol. 2025 Jun 18;13:1558735. doi: 10.3389/fbioe.2025.1558735. eCollection 2025.

DOI:10.3389/fbioe.2025.1558735
PMID:40606909
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12213499/
Abstract

Tissue nanotransfection (TNT) is a novel, non-viral nanotechnology platform that enables gene delivery and direct cellular reprogramming through localized nanoelectroporation. This review synthesizes current advancements in TNT, outlining its device architecture, electroporation principles, and optimized delivery of genetic cargo, including plasmid DNA, mRNA, and CRISPR/Cas9 components. The mechanisms underlying TNT-mediated cellular reprogramming are critically evaluated, including transcriptional activation, epigenetic remodeling, and metabolic shifts, across three major reprogramming strategies-induced pluripotency, direct lineage conversion, and partial cellular rejuvenation. TNT demonstrates transformative therapeutic potential in diverse biomedical applications, including tissue regeneration, ischemia repair, wound healing, immunotherapy, and antimicrobial therapy. This review highlights TNT's unique advantages over traditional gene delivery systems, namely, its high specificity, non-integrative approach, and minimal cytotoxicity, while also addressing existing limitations such as phenotypic stability and scalability. By integrating emerging data and identifying key translation challenges, this work positions TNT as a conceptual and technological advance in regenerative medicine and targeted gene therapy, offering a roadmap for future research and clinical implementation.

摘要

组织纳米转染(TNT)是一种新型的非病毒纳米技术平台,可通过局部纳米电穿孔实现基因递送和直接细胞重编程。本综述综合了TNT的当前进展,概述了其设备架构、电穿孔原理以及遗传物质(包括质粒DNA、mRNA和CRISPR/Cas9组件)的优化递送。对TNT介导的细胞重编程的潜在机制进行了严格评估,包括转录激活、表观遗传重塑和代谢转变,涉及三种主要的重编程策略——诱导多能性、直接谱系转化和部分细胞年轻化。TNT在多种生物医学应用中展现出变革性的治疗潜力,包括组织再生、缺血修复、伤口愈合、免疫治疗和抗菌治疗。本综述强调了TNT相对于传统基因递送系统的独特优势,即其高特异性、非整合方法和最小细胞毒性,同时也探讨了现有局限性,如表型稳定性和可扩展性。通过整合新数据并识别关键的转化挑战,本研究将TNT定位为再生医学和靶向基因治疗的概念和技术进步,为未来的研究和临床应用提供了路线图。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7c8/12213499/1f6bd513b330/fbioe-13-1558735-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7c8/12213499/dd7a81443b69/fbioe-13-1558735-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7c8/12213499/1f6bd513b330/fbioe-13-1558735-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7c8/12213499/dd7a81443b69/fbioe-13-1558735-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7c8/12213499/1f6bd513b330/fbioe-13-1558735-g002.jpg

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Int J Mol Sci. 2025 Mar 27;26(7):3063. doi: 10.3390/ijms26073063.
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Cell reprogramming: methods, mechanisms and applications.细胞重编程:方法、机制与应用
Cell Regen. 2025 Mar 27;14(1):12. doi: 10.1186/s13619-025-00229-x.
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Comprehensive promotion of iPSC-CM maturation by integrating metabolic medium with nanopatterning and electrostimulation.通过将代谢培养基与纳米图案化和电刺激相结合全面促进诱导多能干细胞衍生心肌细胞(iPSC-CM)成熟
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Epigenetic regulation of reprogramming and pluripotency: insights from histone modifications and their implications for cancer stem cell therapies.重编程与多能性的表观遗传调控:来自组蛋白修饰的见解及其对癌症干细胞治疗的意义
Front Cell Dev Biol. 2025 Mar 3;13:1559183. doi: 10.3389/fcell.2025.1559183. eCollection 2025.
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Nature. 2025 Apr;640(8059):828-839. doi: 10.1038/s41586-025-08656-1. Epub 2025 Feb 26.
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Biochem Genet. 2025 Feb 19. doi: 10.1007/s10528-025-11056-9.
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