Puttini Stefania, Lekka Małgorzata, Dorchies Olivier M, Saugy Damien, Incitti Tania, Ruegg Urs T, Bozzoni Irene, Kulik Andrzej J, Mermod Nicolas
Institute of Biotechnology, University of Lausanne, Lausanne, Switzerland.
Mol Ther. 2009 Jan;17(1):19-25. doi: 10.1038/mt.2008.239. Epub 2008 Nov 11.
Dystrophin mediates a physical link between the cytoskeleton of muscle fibers and the extracellular matrix, and its absence leads to muscle degeneration and dystrophy. In this article, we show that the lack of dystrophin affects the elasticity of individual fibers within muscle tissue explants, as probed using atomic force microscopy (AFM), providing a sensitive and quantitative description of the properties of normal and dystrophic myofibers. The rescue of dystrophin expression by exon skipping or by the ectopic expression of the utrophin analogue normalized the elasticity of dystrophic muscles, and these effects were commensurate to the functional recovery of whole muscle strength. However, a more homogeneous and widespread restoration of normal elasticity was obtained by the exon-skipping approach when comparing individual myofibers. AFM may thus provide a quantification of the functional benefit of gene therapies from live tissues coupled to single-cell resolution.
肌营养不良蛋白介导肌纤维细胞骨架与细胞外基质之间的物理连接,其缺失会导致肌肉变性和营养不良。在本文中,我们表明,利用原子力显微镜(AFM)检测发现,肌营养不良蛋白的缺失会影响肌肉组织外植体中单个纤维的弹性,从而对正常和营养不良性肌纤维的特性进行了灵敏且定量的描述。通过外显子跳跃或通过异位表达类肌养蛋白来挽救肌营养不良蛋白的表达,可使营养不良性肌肉的弹性恢复正常,且这些效应与整块肌肉力量的功能恢复程度相当。然而,在比较单个肌纤维时,外显子跳跃方法能使正常弹性得到更均匀、更广泛的恢复。因此,AFM可以定量评估来自活组织且具有单细胞分辨率的基因治疗的功能效益。