Abstract |
The effects of dimethylsulfoxide ( DMSO) on sphingomyelinase activity measured at pH range 3.5-8.0 were examined in normal and Niemann-Pick disease type A, B and C fibroblasts culture. In normal cells, a minor activity was observed at pH 7.5, which was 3- to 4-fold lower than a major one at pH 5.0. Both activities at pH 5.0 and 7.5 were Mg2+-independent and localized to lysosomes. Niemann-Pick type C cells had 30-50% residual sphingomyelinase activity at both pH 5.0 and 7.5, as compared to normal control cells, whereas type A and B cells exhibited virtually no activity over the entire pH range examined. Treatment with 2% DMSO caused a marked increase in sphingomyelinase activities at pH 5.0 and 7.5 in normal and Niemann-Pick disease type C cells, while in type A and B cells, both activities remained virtually unchanged after DMSO treatment. The increase in sphingomyelinase activity at pH 5.0 induced in normal cells by DMSO resulted in an increase in the Vmax without a substantial change in the Km and was inhibited by the simultaneous addition of 10 micrograms/ml of cycloheximide. By comparison, a less than 2-fold increase in other lysosomal hydrolase activities was observed after DMSO treatment in all cell lines examined.
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Authors | M Sato, Y Yoshida, N Sakuragawa, M Arima |
Journal | Biochimica et biophysica acta
(Biochim Biophys Acta)
Vol. 962
Issue 1
Pg. 59-65
(Sep 02 1988)
ISSN: 0006-3002 [Print] Netherlands |
PMID | 2843241
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Cycloheximide
- Phosphoric Diester Hydrolases
- Sphingomyelin Phosphodiesterase
- Dimethyl Sulfoxide
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Topics |
- Cell Line
- Cycloheximide
(pharmacology)
- Dimethyl Sulfoxide
(pharmacology)
- Enzyme Activation
(drug effects)
- Fibroblasts
(drug effects, enzymology, pathology)
- Humans
- Hydrogen-Ion Concentration
- Intracellular Fluid
(drug effects, enzymology)
- Lysosomes
(drug effects, enzymology)
- Niemann-Pick Diseases
(classification, enzymology, pathology)
- Phosphoric Diester Hydrolases
(metabolism)
- Sphingomyelin Phosphodiesterase
(antagonists & inhibitors, metabolism)
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