椎间盘
遗传增强
医学
腰痛
体内
细胞外基质
背痛
生物信息学
病理
外科
基因
细胞生物学
生物
生物技术
生物化学
替代医学
作者
Shirley Tang,Ana I. Salazar‐Puerta,Mary K. Heimann,Kyle Kuchynsky,María A. Rincon‐Benavides,Mia Kordowski,Gilian Gunsch,Lucy Bodine,Khady Diop,Connor Gantt,Safdar N. Khan,Anna Bratasz,Olga N. Kokiko‐Cochran,Julie Fitzgerald,Damien M. Laudier,Judith A. Hoyland,Benjamin A. Walter,Natalia Higuita‐Castro,Devina Purmessur
出处
期刊:Biomaterials
[Elsevier]
日期:2024-04-01
卷期号:308: 122562-122562
标识
DOI:10.1016/j.biomaterials.2024.122562
摘要
Painful musculoskeletal disorders such as intervertebral disc (IVD) degeneration associated with chronic low back pain (termed "Discogenic back pain", DBP), are a significant socio-economic burden worldwide and contribute to the growing opioid crisis. Yet there are very few if any successful interventions that can restore the tissue's structure and function while also addressing the symptomatic pain. Here we have developed a novel non-viral gene therapy, using engineered extracellular vesicles (eEVs) to deliver the developmental transcription factor FOXF1 to the degenerated IVD in an in vivo model. Injured IVDs treated with eEVs loaded with FOXF1 demonstrated robust sex-specific reductions in pain behaviors compared to control groups. Furthermore, significant restoration of IVD structure and function in animals treated with FOXF1 eEVs were observed, with significant increases in disc height, tissue hydration, proteoglycan content, and mechanical properties. This is the first study to successfully restore tissue function while modulating pain behaviors in an animal model of DBP using eEV-based non-viral delivery of transcription factor genes. Such a strategy can be readily translated to other painful musculoskeletal disorders.
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