Inhibition of myoblast fusion by bromoconduritol
| Autor: | Paul C. Holland, Annette Herscovics, Geralyn C. Trudel |
|---|---|
| Rok vydání: | 1988 |
| Předmět: |
Mannosidase
1-Deoxynojirimycin Plating efficiency Biology Biochemistry Catalysis Cell Line Cell Fusion Myoblast fusion Cyclohexenes Animals Myocyte Lactoperoxidase Molecular Biology Bromoconduritol Gel electrophoresis Glucosamine Cell growth Muscles Membrane Proteins Cell Biology Molecular biology Anti-Bacterial Agents Rats Molecular Weight Covalent bond Glucosidases Inositol |
| Zdroj: | Biochemistry and Cell Biology. 66:1119-1125 |
| ISSN: | 1208-6002 0829-8211 |
| DOI: | 10.1139/o88-129 |
| Popis: | It has recently been reported that the glucosidase I inhibitor, N-methyl- 1-deoxynojirimycin (MDJN), inhibits myoblast fusion whereas the mannosidase inhibitor, 1 -deoxymannojirimycin (ManDJN), has no effect on fusion. We now report that bromoconduritol, which is an active-site-directed covalent inhibitor of glucosidase II, also inhibits fusion at concentrations that have no effect on the plating efficiency or growth of rat L6 myoblasts. Significant inhibition of fusion was obtained at concentrations as low as 50 μg of bromoconduritol/mL, whereas inhibition of cell growth did not occur until concentrations of 250 μg/mL were reached. Rat L6 myoblasts were grown in the presence and absence of processing inhibitors and were surface labelled with 125I. Analysis of the iodinated proteins by two-dimensional gel electrophoresis demonstrated that a number of high-molecular-weight proteins (>90 000) detected at the surface of control cells were absent from the surface of cells treated with MDJN or bromoconduritol. It is suggested that MDJN and bromoconduritol prevent the translocation of these proteins to the cell surface. The high-molecular-weight proteins detected at the surface of control cells were also detectable in ManDJN-treated cells, indicating that inhibition of N-linked complex oligosaccharide formation does not affect the translocation of these proteins to the myoblast cell surface. |
| Databáze: | OpenAIRE |
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