White Tom, López-Márquez Arístides, Badosa Carmen, Jimenez-Mallebrera Ceclila, Samitier Josep, Giannotti Marina Inés, Lagunas Anna
Nanobioengineering Group, Institute for Bioengineering of Catalonia (IBEC), The Barcelona Institute for Science and Technology (BIST), Barcelona, Spain.
Laboratorio de Investigación Aplicada en Enfermedades Neuromusculares, Institut de Recerca Sant Joan de Déu, Barcelona, Catalunya, Spain.
J R Soc Interface. 2025 Mar;22(224):20240860. doi: 10.1098/rsif.2024.0860. Epub 2025 Mar 12.
Changes in the mechanical properties of the extracellular matrix (ECM) are a hallmark of disease. Due to its relevance, several models have been developed for the ECM, including cell-derived matrices (CDMs). CDMs are decellularized natural ECMs assembled by cells that closely mimic the stromal fibre organization and molecular content. Here, we applied atomic force microscopy-force spectroscopy (AFM-FS) to evaluate the nanomechanical properties of CDMs obtained from patients diagnosed with collagen VI-related congenital muscular dystrophies (COL6-RDs). COL6-RDs are a set of neuromuscular conditions caused by pathogenic variants in any of the three major COL6 genes, which result in deficiency or dysfunction of the COL6 incorporated into the ECM of connective tissues. Current diagnosis includes the genetic confirmation of the disease and categorization of the phenotype based on maximum motor ability, as no direct correlation exists between genotype and phenotype of COL6-RDs. We describe differences in the elastic modulus () among CDMs from patients with different clinical phenotypes, as well as the restoration of in CDMs obtained from genetically edited cells. Results anticipate the potential of the nanomechanical analysis of CDMs as a complementary clinical tool, providing phenotypic information about COL6-RDs and their response to gene therapies.
细胞外基质(ECM)力学性质的改变是疾病的一个标志。鉴于其相关性,已经开发了几种针对ECM的模型,包括细胞衍生基质(CDM)。CDM是由细胞组装而成的脱细胞天然ECM,其紧密模拟基质纤维组织和分子含量。在这里,我们应用原子力显微镜-力谱(AFM-FS)来评估从被诊断患有与胶原蛋白VI相关的先天性肌营养不良症(COL6-RD)的患者中获得的CDM的纳米力学性质。COL6-RD是一组神经肌肉疾病,由三个主要COL6基因中任何一个的致病变异引起,这些变异导致整合到结缔组织ECM中的COL6缺乏或功能障碍。目前的诊断包括疾病的基因确认和基于最大运动能力的表型分类,因为COL6-RD的基因型和表型之间不存在直接相关性。我们描述了来自不同临床表型患者的CDM之间弹性模量()的差异,以及从基因编辑细胞获得的CDM中弹性模量的恢复情况。结果预示了CDM纳米力学分析作为一种补充临床工具的潜力,可提供有关COL6-RD及其对基因治疗反应的表型信息。