Literature DB >> 8397379

[Value of skin fibroblasts in culture for the diagnosis of mitochondrial cell dysfunction. Apropos of 5 cases with cytochrome c oxidase deficiency].

J M Collombet1, M T Zabot, M Vidailhet, I Maire, B Echenne, J Floquet, R Dumoulin, M Rimoldi, M Mathieu, B Mousson.   

Abstract

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.

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Year:  1993        PMID: 8397379

Source DB:  PubMed          Journal:  Pediatrie        ISSN: 0031-4021


  2 in total

1.  2-Ketoglutarate dehydrogenase deficiency, a rare cause of primary hyperlactataemia: report of a new case.

Authors:  N Guffon; C Lopez-Mediavilla; R Dumoulin; B Mousson; C Godinot; H Carrier; J M Collombet; P Divry; M Mathieu; P Guibaud
Journal:  J Inherit Metab Dis       Date:  1993       Impact factor: 4.982

2.  Light and electron microscopy characteristics of the muscle of patients with SURF1 gene mutations associated with Leigh disease.

Authors:  M Pronicki; E Matyja; D Piekutowska-Abramczuk; T Szymanska-Debinska; A Karkucinska-Wieckowska; E Karczmarewicz; W Grajkowska; T Kmiec; E Popowska; J Sykut-Cegielska
Journal:  J Clin Pathol       Date:  2007-10-01       Impact factor: 3.411

  2 in total

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