Myotonic muscular dystrophy
- 1 June 1979
- journal article
- research article
- Published by Wolters Kluwer Health in Neurology
- Vol. 29 (6) , 791
- https://doi.org/10.1212/wnl.29.6.791
Abstract
The activities of the membrane-bound protein kinases of the human erythrocyte membrane that phosphorylate spectrin, band-3 protein, and phospholipids were compared in patients with myotonic muscular dystrophy and normal age-and sex-matched controls. These activities tended to be lower in the patients, but the differences were not statistically significant. In contrast, the temperature responses (the increase in activity in response to an increase in temperature from 30° C to 37° C) of the spectrin and band-3 protein kinase activities were significantly lower in the patients. Although they do not eliminate an alteration of one of the substrates, these results are consistent with the proposal that differences in erythrocytes from myotonic muscular dystrophy (MyD) patients are due to a membrane lipid change. Cholesterol is unlikely to be the altered lipid, as no difference in membrane cholesterol content was found.This publication has 3 references indexed in Scilit:
- Vertical displacement of membrane proteins mediated by changes in microviscosity.Proceedings of the National Academy of Sciences, 1976
- Erythrocyte spectrin peak II phosphorylation in Duchenne muscular dystrophyJournal of the Neurological Sciences, 1976
- Platelet Sequestration in Man. I. Methods*Journal of Clinical Investigation, 1964