生物
祖细胞
细胞生物学
离体
干细胞
造血
转基因生物
遗传增强
基因传递
转基因
再生医学
基因工程
组织工程
免疫学
移植
再生(生物学)
基因组编辑
脚手架
基因
细胞分化
基因治疗载体
细胞培养
转染
祖细胞
造血干细胞
癌症研究
合成生物学
诱导多能干细胞
异种移植
基因靶向
分子生物学
重编程
细胞骨架
作者
Federico Midena,Laura Alessandrini,Claudio Conci,Matteo Barcella,Francesco Gazzo,Emanuela Jacchetti,Edoardo Carsana,Fabrizio Benedicenti,Roberta Vacca,Lucrezia della Volpe,Sergio Arévalo,Kety Giannetti,Dafne Barozzi,Martina Franchino,Erika Zonari,Francesca Ferrua,Giacomo Farina,Chiara Brombin,Federica Cugnata,Martina Fiumara
出处
期刊:Cell Stem Cell
[Elsevier BV]
日期:2026-01-08
卷期号:33 (2): 217-232.e9
被引量:2
标识
DOI:10.1016/j.stem.2025.12.016
摘要
Ex vivo culture of hematopoietic stem and progenitor cells (HSPCs) is required for gene therapy applications but inadvertently triggers detrimental cellular responses, potentially threatening clinical success. In this study, we employ nichoids, biocompatible 3D culture substrates with cell-scale resolution, to provide HSPCs with mechanical support during ex vivo manipulation. This innovative 3D system improves HSPC multi-lineage differentiation and engraftment capacity by leveraging mechanobiological control over nuclear morphology, cytoskeleton organization, metabolism, and DNA integrity. Notably, 3D culture enables efficient genetic engineering across multiple platforms, including long-range gene editing, base- and prime-editing, and lentiviral-mediated gene addition. Moreover, this scaffold increases the clonal output and persistence of genetically engineered cells in xenotransplantation experiments, including a clinical protocol for lentiviral gene addition in Wiskott-Aldrich syndrome. Overall, we propose a transformative approach to enhance the efficacy and safety of emerging and established hematopoietic stem cell-based gene therapy applications.
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