Collombet J M, Zabot M T, Vidailhet M, Maire I, Echenne B, Floquet J, Dumoulin R, Rimoldi M, Mathieu M, Mousson B
Centre d'étude des maladies métaboliques, Hôpital Debrousse, Lyon.
Pediatrie. 1993;48(4):287-95.
Mitochondrial respiratory chain dysfunction has been studied by two complementary methods using cultured skin fibroblasts from five patients with muscular cytochrome c oxidase (complex IV) deficiency: first, a screening test measuring lactate to pyruvate ratio (L/P) after supplementation of cultured cells; secondly, measurement of complex IV activity in whole cells. Respiratory chain defect (increased L/P ratio with decreased complex IV activity) was expressed in fibroblasts of four of the five patients. Our results show that skin fibroblasts can be helpful for biochemical diagnosis of mitochondrial respiratory chain defects.
利用来自5例肌肉细胞色素c氧化酶(复合体IV)缺乏症患者的培养皮肤成纤维细胞,通过两种互补方法对线粒体呼吸链功能障碍进行了研究:第一,一种筛选试验,在培养细胞补充后测量乳酸与丙酮酸的比率(L/P);第二,测量全细胞中的复合体IV活性。呼吸链缺陷(L/P比率升高且复合体IV活性降低)在5例患者中的4例成纤维细胞中表现出来。我们的结果表明,皮肤成纤维细胞有助于线粒体呼吸链缺陷的生化诊断。