From Inserm UMR_S 910 Génétique Médicale et Génomique Fonctionnelle, Université de la Méditerranée, Faculté de Médecine de Marseille, France.
Neuromuscul Disord. 2010 Jan;20(1):57-60. doi: 10.1016/j.nmd.2009.08.004. Epub 2009 Oct 23.
Dysferlinopathies are autosomal recessive muscular dystrophies caused by DYSF mutations, which lead to a reduced amount or a complete lack of dysferlin. One step in dysferlinopathies diagnosis consists in Western blot analysis of proteins extracted from muscle biopsy, or blood monocytes. We have taken advantage of dysferlin expression in monocytes to develop a whole blood flow cytometry (WBFC), using antibodies directed against dysferlin. Six patients were submitted to WBFC analysis and immunofluorescence analysis on monocytes. Results obtained are correlated to Western blot from monocytes and muscle biopsies. The possible usefulness of this flow cytometry analysis in routine diagnosis is presented.
肌营养不良蛋白病是由 DYSF 突变引起的常染色体隐性肌肉营养不良症,导致肌营养不良蛋白数量减少或完全缺失。肌营养不良蛋白病诊断的一个步骤包括对肌肉活检或血液单核细胞中提取的蛋白质进行 Western blot 分析。我们利用单核细胞中肌营养不良蛋白的表达,开发了一种使用针对肌营养不良蛋白的抗体的全血流式细胞术(WBFC)。六名患者接受了单核细胞 WBFC 分析和免疫荧光分析。将获得的结果与单核细胞和肌肉活检的 Western blot 进行相关分析。本文介绍了这种流式细胞术分析在常规诊断中的可能用途。