Abstract
Inhibitors of lysosomal acidification (4,4'-di-isothiocyanostilbene-2,2'-disulphonate, NN'-dicyclohexylcarbodi-imide, carbonyl cyanide m-chlorophenylhydrazone, NH4Cl and methylamine hydrochloride) did not alter cystine egress or countertransport in polymorphonuclear-leucocyte lysosome-rich granular fractions at pH 7.0. Together, 2 mM-MgCl2/MgATP and 90 mM-KCl stimulated cystine egress 2-fold, but this effect also was not influenced by inhibitors of ATP-dependent lysosomal acidification. MgCl2/MgATP stimulated cystine transport at pH 5.5, but the effect also occurred with MgCl2, MgSO4 or MnCl2 alone, was prevented by chelation, and was not seen with NaATP; therefore, it was considered a bivalent-cation, not an ATP, effect. Proton-pump-mediated acidification of lysosomes does not appear to be required for cystine transport in normal polymorphonuclear-leucocyte granular fractions, as reported for lymphoblast lysosomes.
MeSH Terms
Adenosine Triphosphate/pharmacology
Biological Transport
Cystine/metabolism
Enzyme Inhibitors/pharmacology
Humans
Hydrogen-Ion Concentration
Leukocytes/drug effects,metabolism
Lysosomes/drug effects,metabolism
Magnesium/pharmacology
Chemicals
Enzyme Inhibitors
Cystine
Adenosine Triphosphate
Magnesium
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Gahl W A
Tietze F
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14 references, click to expand
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