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Flow Cytometric Evaluation of Defects of the Mitochondrial Respiratory Chain

Department of Paediatrics and Child Health, University of Sydney Sydney, Australia, Department of Clinical Biochemistry, Royal Alexandra Hospital for Children, Westmead, Australia

John C. Coakley, FRACP, MD

Department of Clinical Biochemistry, Royal Alexandra Hospital for Children, Westmead, Australia

John Christodoulou, FRACP, PhD

Department of Paediatrics and Child Health, University of Sydney Sydney, Australia, johnch{at}mail.usyd.edu.au, Western Sydney Genetics Program Royal Alexandra Hospital for Children, Westmead, Australia

Cultured human skin fibroblasts from 12 patients with a variety of mitochondrial respiratory chain defects were examined for their capacity to oxidize dihydrorhodamine-123 to the fluorescent molecule rhodamine-123 using a flow cytometer. We found that cells from patients with functional defects in respiratory chain enzymes were less able to oxidize dihydrorhodamine-123 than those of healthy controls. Ten of the cell strains had reduced activity in at least one of the respiratory chain complexes and also showed significantly reduced fluorescence when compared to the mean of eight normal control cell strains. One patient had mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (with the A3243G mutation) and reduced respiratory chain activities in muscle and liver. Molecular analysis did not show the mutation in cultured skin fibroblasts, and had correspondingly normal fluorescence. The 12th cell strain showed reduced fluorescence but did not reach statistical significance. This strategy could be of use in helping direct further investigations in patients, and in studying the biochemical pathogenesis of mitochondrial DNA mutations in cybrid studies. (J Child Neurol 1999;14:518-523).

Journal of Child Neurology, Vol. 14, No. 8, 518-523 (1999)
DOI: 10.1177/088307389901400807


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