Shahin-Shamsabadi Alireza, Cappuccitti John
Evolved.Bio, 280 Joseph Street, Kitchener, Ontario, N2G4Z5, Canada.
Adv Healthc Mater. 2025 May;14(12):e2404465. doi: 10.1002/adhm.202404465. Epub 2024 Dec 24.
Progress in understanding the underlying mechanisms of muscular dystrophies is hindered by the lack of pathophysiologically relevant in vitro models. Here, an entirely scaffold-free anchored cell sheet engineering platform is used to create patient-specific three-dimensional (3D) skeletal muscle in vitro models. This approach effectively replicates mature muscle phenotypes and tissue- and disease-specific extracellular matric (ECM). Models were developed using primary cells from healthy individuals and patients with Duchenne Muscular Dystrophy and Myotonic Dystrophy Type 1. Through a combination of quantified histological staining (Hematoxylin & Eosin, Movat's Pentachrome, Masson's Trichrome) and immunostaining (desmin, myosin heavy chain, laminin, and dystrophin), it was demonstrated that the models formed mature constructs closely resembling their respective in vivo conditions. Proteomics analysis revealed that the models exhibited appropriate upregulation and downregulation of disease-relevant pathways. Models of diseased tissues accurately reflected key phenotypic features of the diseases, including alterations in muscle fiber integrity and ECM composition. Upon treatment with therapeutically beneficial drugs, significant changes in their proteomic profiles were documented, highlighting the models' potential for drug screening. This novel in vitro modeling approach, unlike other 3D techniques that rely on exogenous biomaterials that interfere with natural cellular behaviors, provides a promising platform for studying muscular dystrophies.
由于缺乏病理生理学相关的体外模型,对肌肉营养不良潜在机制的理解进展受到阻碍。在此,一个完全无支架的锚定细胞片工程平台被用于创建患者特异性的三维(3D)骨骼肌体外模型。这种方法有效地复制了成熟肌肉表型以及组织和疾病特异性的细胞外基质(ECM)。使用来自健康个体以及杜氏肌营养不良症和1型强直性肌营养不良症患者的原代细胞开发了模型。通过定量组织学染色(苏木精和伊红染色、莫瓦特五色染色、马松三色染色)和免疫染色(结蛋白、肌球蛋白重链、层粘连蛋白和抗肌萎缩蛋白)相结合的方法,证明这些模型形成了与各自体内情况极为相似的成熟结构。蛋白质组学分析表明,这些模型展示了疾病相关通路的适当上调和下调。患病组织模型准确反映了疾病的关键表型特征,包括肌纤维完整性和ECM组成的改变。在用具有治疗益处的药物处理后,记录到它们的蛋白质组学图谱有显著变化,突出了这些模型在药物筛选方面的潜力。这种新型体外建模方法不同于其他依赖外源性生物材料且会干扰自然细胞行为的3D技术,为研究肌肉营养不良症提供了一个有前景的平台。