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PMID: 2525560 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Impaired lysosomes in a temperature-sensitive mutant of Chinese hamster ovary cells.

The Journal of cell biology ·Vol. 108 ·No. 6 ·1989-06-00 ·Pages 2211-9

Colbaugh PA, Stookey M, Draper RK

Abstract

We describe here the properties of a mutant of Chinese hamster ovary cells that expresses a conditional-lethal mutation affecting dense lysosomes. This mutant, termed V.24.1, is a member of the End4 complementation group of temperature-sensitive mutants selected for resistance to protein toxins (Colbaugh, P. A., C.-Y. Kao, S.-P. Shia, M. Stookey, and R. K. Draper. 1988. Somatic Cell Mol. Genet. 14:499-507). Vesicles present in postnuclear supernatants prepared from V.24.1 cells harvested at the restrictive temperature had a 50% reduction in acidification activity, assessed by the ATP-stimulated accumulation of the dye acridine orange in acidic vesicles. To investigate whether specific populations of vesicles were impaired in acidification, we measured acidification activity in three subcellular fractions prepared from Percoll gradients: one containing endosomal and Golgi markers, one containing buoyant lysosomes, and the third containing dense lysosomes. Activity in dense lysosomes was reduced by 90%, activity in the buoyant lysosome fraction was unaffected, and activity in the endosome-Golgi fraction was mildly reduced. The activity of three lysosomal enzymes--beta-hexosaminidase, beta-galactosidase, and beta-glucocerebrosidase--was also reduced in dense lysosomes but nearly normal in the buoyant lysosome fraction. However, beta-hexosaminidase and beta-glucocerebrosidase activity was increased two- to threefold in the endosome-Golgi fraction. We conclude that the lesion selectively impairs dense lysosomes but has little effect on properties of buoyant lysosomes.

MeSH Terms
Adenosine Triphosphate/metabolism Animals Cell Compartmentation Cell Line Cricetinae Diphtheria Toxin/toxicity Drug Resistance Endocytosis Hydrogen-Ion Concentration Iron/pharmacology Lectins/toxicity Lysosomes/enzymology,physiology Mutation Plant Lectins Receptors, Transferrin/metabolism Ribosome Inactivating Proteins, Type 2 Subcellular Fractions/enzymology Temperature Time Factors Transferrin/metabolism beta-N-Acetylhexosaminidases/metabolism
Chemicals
Diphtheria Toxin Lectins Plant Lectins Receptors, Transferrin Ribosome Inactivating Proteins, Type 2 Transferrin modeccin Adenosine Triphosphate Iron beta-N-Acetylhexosaminidases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Colbaugh P A
Biology Programs, University of Texas, Dallas, Richardson 75083-0688.
Stookey M
Draper R K
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35 references, click to expand
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Article Info
Journal
The Journal of cell biology
Abbr.
J Cell Biol
ISSN
0021-9525
Published
1989-06-00
Pages
2211-9
Language
English
Region
United States
NLM ID
0375356
PMCID
PMC2115610
Subset
IM
Grants
NIGMS NIH HHS · GM34297 · United States
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