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. 1985 Jun 15;228(3):545–550. doi: 10.1042/bj2280545

Cysteamine depletes cystinotic leucocyte granular fractions of cystine by the mechanism of disulphide interchange.

W A Gahl, F Tietze, J D Butler, J D Schulman
PMCID: PMC1145021  PMID: 4026796

Abstract

Cystinotic lysosome-rich leucocyte granular fractions, loaded with [35S]cystine, were exposed to different cystine-depleting agents. During a 30 min incubation at 37 degrees C, untreated cystinotic granular fractions lost negligible [35S]cystine when corrected for lysosome rupture. Granular fractions exposed to 0.1 mM-cysteamine lost 64% of their initial cystine, and hexosaminidase activity was decreased by 10%. This was accompanied by the formation of high concentrations of [35S]cysteine-cysteamine mixed disulphide within the granular-fraction pellet, and, in the presence of N-ethylmaleimide, increasing amounts of [35S]cysteine-N-ethylmaleimide adduct outside the granular fraction. In separate experiments, [35S]cystine exited cystinotic leucocyte lysosomes at a negligible rate (half-times 199 and 293 min), but [35S]cysteine-cysteamine mixed disulphide exhibited substantial egress (half-times 66 and 88 min) and was recovered intact outside the granular-fraction pellet. We conclude that cysteamine depletes lysosomes of cystine by participating in a thiol-disulphide interchange reaction to produce cysteine and cysteine-cysteamine mixed disulphide, both of which traverse the cystinotic leucocyte lysosomal membrane.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Gahl W. A., Bashan N., Tietze F., Bernardini I., Schulman J. D. Cystine transport is defective in isolated leukocyte lysosomes from patients with cystinosis. Science. 1982 Sep 24;217(4566):1263–1265. doi: 10.1126/science.7112129. [DOI] [PubMed] [Google Scholar]
  2. Gahl W. A., Tietze F., Bashan N., Bernardini I., Raiford D., Schulman J. D. Characteristics of cystine counter-transport in normal and cystinotic lysosome-rich leucocyte granular fractions. Biochem J. 1983 Nov 15;216(2):393–400. doi: 10.1042/bj2160393. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Gahl W. A., Tietze F., Bashan N., Steinherz R., Schulman J. D. Defective cystine exodus from isolated lysosome-rich fractions of cystinotic leucocytes. J Biol Chem. 1982 Aug 25;257(16):9570–9575. [PubMed] [Google Scholar]
  4. Goldman H., Scriver C. R., Aaron K., Pinsky L. Use of dithiothreitol to correct cystine storage in cultured cystinotic fibroblasts. Lancet. 1970 Apr 18;1(7651):811–812. doi: 10.1016/s0140-6736(70)92411-6. [DOI] [PubMed] [Google Scholar]
  5. Kroll W. A., Schneider J. A. Decrease in free cystine content of cultured cystinotic fibroblasts by ascorbic acid. Science. 1974 Dec 13;186(4168):1040–1042. doi: 10.1126/science.186.4168.1040. [DOI] [PubMed] [Google Scholar]
  6. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  7. Schneider J. A., Schlesselman J. J., Mendoza S. A., Orloff S., Thoene J. G., Kroll W. A., Godfrey A. D., Schulman J. D. Ineffectiveness of ascorbic acid therapy in nephropathic cystinosis. N Engl J Med. 1979 Apr 5;300(14):756–759. doi: 10.1056/NEJM197904053001403. [DOI] [PubMed] [Google Scholar]
  8. Schulman J. D., Bradley K. H. The metabolism of amino acids, peptides, and disulfides in lysosomes of fibroblasts cultured from normal individuals and those with cystinosis. J Exp Med. 1970 Dec 1;132(6):1090–1104. doi: 10.1084/jem.132.6.1090. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Steinherz R., Tietze F., Raiford D., Gahl W. A., Schulman J. D. Patterns of amino acid efflux from isolated normal and cystinotic human leucocyte lysosomes. J Biol Chem. 1982 Jun 10;257(11):6041–6049. [PubMed] [Google Scholar]
  10. Thoene J. G., Oshima R. G., Crawhall J. C., Olson D. L., Schneider J. A. Cystinosis. Intracellular cystine depletion by aminothiols in vitro and in vivo. J Clin Invest. 1976 Jul;58(1):180–189. doi: 10.1172/JCI108448. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Weisgraber K. H., Innerarity T. L., Mahley R. W. Abnormal lipoprotein receptor-binding activity of the human E apoprotein due to cysteine-arginine interchange at a single site. J Biol Chem. 1982 Mar 10;257(5):2518–2521. [PubMed] [Google Scholar]

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