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Carnitine transport in cultured muscle cells and skin fibroblasts from patients with primary systemic carnitine deficiency

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l-Carnitine transport was studied in cultured muscle cells and skin fibroblasts of patients with primary systemic carnitine deficiency and control subjects. In both cell culture types, two systems for carnitine transport were identified. The kinetic parameters for carnitine transport were remarkably similar in cultured muscle cells and skin fibroblasts. Normal rates and kinetic properties of carnitine transport were observed for both cell lines from patients with systemic carnitine deficiency. These studies do not rule out a defect in carnitine transport in vivo.

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References

  1. Rebouche, C. J.; Engel, A. G. Tissue distribution of carnitine biosynthetic enzymes in man. Biochim. Biophys. Acta 630: 22–29; 1980.

    PubMed  CAS  Google Scholar 

  2. Rebouche, C. J. Carnitine movement across muscle cell membranes. Studies in isolated rat muscle. Biochim. Biophys. Acta 471: 145–155; 1977.

    Article  PubMed  CAS  Google Scholar 

  3. Engel, A. G.; Rebouche, C. J. Pathogenetic mechanisms in human carnitine deficiency syndromes. Schotland, D. L. ed. Disorders of the motor unit. New York: John Wiley & Sons; 1982: 643–656.

    Google Scholar 

  4. Rebouche, C. J.; Engel, A. G. In vitro analysis of hepatic carnitine biosynthesis in human systemic carnitine deficiency. Clin. Chim. Acta 106: 295–300; 1980.

    Article  PubMed  CAS  Google Scholar 

  5. Rebouche, C. J.; Engel, A. G. Primary systemic carnitine deficiency. I. Carnitine biosynthesis. Neurology (NY) 31: 813–818; 1981.

    CAS  Google Scholar 

  6. Engel, A. G.; Rebouche, C. J.; Wilson, D. M.; Glasgow, A. M.; Romshe, C. A.; Cruse, R. P. Primary systemic carnitine deficiency. II. Renal handling of carnitine. Neurology (NY) 31: 819–825; 1981.

    CAS  Google Scholar 

  7. Stokke, O.; Bremer, J. A simple method for preparation of methyl-labelled (−)carnitine. Biochim. Biophys. Acta 218: 552–554; 1970.

    PubMed  CAS  Google Scholar 

  8. Glasgow, A. M.; Eng, G.; Engel, A. G. Systemic carnitine deficiency simulating recurrent Reye syndrome. J. Pediatr. 96: 889–891; 1980.

    Article  PubMed  CAS  Google Scholar 

  9. Witkowski, J. A.; Durbridge, M.; Dubowitz, V. Growth of human muscle in tissue culture. An improved technique. In Vitro 12: 98–106; 1976.

    Article  Google Scholar 

  10. Diamond, I.; Kennedy, E. P. Carrier-mediated transport of choline into synaptic nerve endings. J. Biol. Chem. 244: 3258–3263; 1969.

    PubMed  CAS  Google Scholar 

  11. Lowry, O. H.; Rosenbrough, N. J.; Farr, A. L.; Randall, R. J. Protein measurement with the Folin-phenol reagent. J. Biol. Chem. 193: 265–275; 1951.

    PubMed  CAS  Google Scholar 

  12. Neal, J. L. Analysis of Michaelis kinetics for two independent, saturable membrane transport functions. J. Theor. Biol. 35: 113–118; 1972.

    Article  PubMed  CAS  Google Scholar 

  13. Karpati, G.; Carpenter, S.; Engel, A. G.; Watters, G.; Allen, J.; Rothman, S.; Klassen, G.; Mamer, O. A. The syndrome of systemic carnitine deficiency. Clinical, morphologic, biochemical and pathophysiologic features. Neurology (NY) 25: 16–24; 1975.

    CAS  Google Scholar 

  14. Rebouche, C. J. Engel, A. G. Carnitine biosynthesis in humans. Schotland, D. L. ed. Disorders of the motor unit. New York: John Wiley & Sons; 1982: 629–641.

    Google Scholar 

  15. Miranda, A. F.; DiMauro, S.; Antler, A.; Stern, L. Z.; Rowland, L. P. Glycogen debrancher deficiency is reproduced in muscle culture. Ann. Neurol. 9: 283–288; 1981.

    Article  PubMed  CAS  Google Scholar 

  16. Askanas, V.; Engel, W. K.; DiMauro, S.; Brooks, B. R.; Mehler, M. Adult-onset acid maltase deficiency. Morphologic and biochemical abnormalities reproduced in cultured muscle. New Eng. J. Med. 294: 573–578; 1976.

    Article  Google Scholar 

  17. DiMauro, S.; Miranda, A. F.; Hays, A. P.; Frank, W. A.; Hoffman, G. S.; Schoenfeldt, R. S.; Singh, N. Myoadenylate deaminase deficiency. Muscle biopsy and muscle culture in a patient with gout. J. Neurol. Sci. 47: 191–202; 1980.

    Article  PubMed  CAS  Google Scholar 

  18. Sammons, D. W.; Chilson, O. P. AMP deaminase: stage-specific isozymes in differentiating chick muscle. Arch. Biochem. Biophys. 191: 561–570; 1978.

    Article  PubMed  CAS  Google Scholar 

  19. Meienhofer, M. C. Askanas, V.; Proux-Daegelen, M. S.; Dreyfus, J. C.; Engel, W. K. Muscle-type phosphorylase activity present in muscle cells cultured from three patients with myophosphorylase deficiency. Arch. Neurol. 34: 779–781; 1977.

    PubMed  CAS  Google Scholar 

  20. Sato, K.; Imai, F.; Hatayama, I.; Roelofs, R. I. Characterization of glycogen phosphorylase isoenzymes present in cultured skeletal muscle from patients with McArdle’s disease. Biochem. Biophys. Res. Commun. 78: 663–668; 1977.

    Article  PubMed  CAS  Google Scholar 

  21. DiMauro, S.; Arnold, S.; Miranda, A.; Rowland, L. P. McArdle disease: the mystery of reappearing phosphorylase activity in muscle culture—a fetal isoenzyme. Ann. Neurol. 3: 60–66; 1978.

    Article  PubMed  CAS  Google Scholar 

  22. Osame, M.; Engel, A. G.; Rebouche, C. J.; Scott, R. E. Freeze-fracture electron microscopic analysis of plasma membranes of cultured muscle cells in Duchenne dystrophy. Neurology (NY) 31: 972–979; 1981.

    CAS  Google Scholar 

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This study was supported by research grants AM27451 and NS06277 from the National Institutes of Health and by a Research Center Grant from the Muscular Dystrophy Association.

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Rebouche, C.J., Engel, A.G. Carnitine transport in cultured muscle cells and skin fibroblasts from patients with primary systemic carnitine deficiency. In Vitro Cell.Dev.Biol.-Plant 18, 495–500 (1982). https://doi.org/10.1007/BF02796479

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  • DOI: https://doi.org/10.1007/BF02796479

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