Abstract
The requirement of cholesterol for myoblast fusion has been linked to the primary step in the fusion process, calcium-dependent aggregation (recognition). Inhibition of cholesterol synthesis with 25- hydroxycholesterol or compactin in the absence of exogenous lipid dramatically inhibits calcium-mediated aggregation and concomitant fusion within several hours. Restimulating cholesterol synthesis or supplying exogenous cholesterol rapidly restores aggregation activity. Over this time period, however, the sterol:phospholipid ratio is unaltered, suggesting a local rather than a general membrane cholesterol requirement for the expression of aggregation activity. The aggregation response to a change in sterol availability occurs on a shorter time scale than that required to inhibit the synthesis of the protein(s) with aggregation activity; thus, the cholesterol-requiring step is posttranslational. We suggest that the assembly or maintenance of the aggregation activity depends on a continued local supply of cholesterol.
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Selected References
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- BARTLETT G. R. Phosphorus assay in column chromatography. J Biol Chem. 1959 Mar;234(3):466–468. [PubMed] [Google Scholar]
- Bell J. J., Sargeant T. E., Watson J. A. Inhibition of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity in hepatoma tissue culture cells by pure cholesterol and several cholesterol derivatives. Evidence supporting two distinct mechanisms.20l. J Biol Chem. 1976 Mar 25;251(6):1745–1758. [PubMed] [Google Scholar]
- Brown M. S., Faust J. R., Goldstein J. L., Kaneko I., Endo A. Induction of 3-hydroxy-3-methylglutaryl coenzyme A reductase activity in human fibroblasts incubated with compactin (ML-236B), a competitive inhibitor of the reductase. J Biol Chem. 1978 Feb 25;253(4):1121–1128. [PubMed] [Google Scholar]
- Cornell R. B., Horwitz A. F. Apparent coordination of the biosynthesis of lipids in cultured cells: its relationship to the regulation of the membrane sterol:phospholipid ratio and cell cycling. J Cell Biol. 1980 Sep;86(3):810–819. doi: 10.1083/jcb.86.3.810. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Devreotes P. N., Gardner J. M., Fambrough D. M. Kinetics of biosynthesis of acetylcholine receptor and subsequent incorporation into plasma membrane of cultured chick skeletal muscle. Cell. 1977 Mar;10(3):365–373. doi: 10.1016/0092-8674(77)90023-x. [DOI] [PubMed] [Google Scholar]
- Freeman C. P., West D. Complete separation of lipid classes on a single thin-layer plate. J Lipid Res. 1966 Mar;7(2):324–327. [PubMed] [Google Scholar]
- HAVEL R. J., EDER H. A., BRAGDON J. H. The distribution and chemical composition of ultracentrifugally separated lipoproteins in human serum. J Clin Invest. 1955 Sep;34(9):1345–1353. doi: 10.1172/JCI103182. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Horwitz A. F., Wight A., Ludwig P., Cornell R. Interrelated lipid alterations and their influence on the proliferation and fusion of cultured myogenic cells. J Cell Biol. 1978 May;77(2):334–357. doi: 10.1083/jcb.77.2.334. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kandutsch A. A., Chen H. W. Regulation of sterol synthesis in cultured cells by oxygenated derivatives of cholesterol. J Cell Physiol. 1975 Apr;85(2 Pt 2 Suppl 1):415–424. doi: 10.1002/jcp.1040850408. [DOI] [PubMed] [Google Scholar]
- Kent C., Schimmel S. D., Vagelos P. R. Lipid composition of plasma membranes from developing chick muscle cells in culture. Biochim Biophys Acta. 1974 Sep 19;360(3):312–321. doi: 10.1016/0005-2760(74)90061-7. [DOI] [PubMed] [Google Scholar]
- Knudsen K. A., Horwitz A. F. Differential inhibition of myoblast fusion. Dev Biol. 1978 Oct;66(2):294–307. doi: 10.1016/0012-1606(78)90239-7. [DOI] [PubMed] [Google Scholar]
- Knudsen K. A., Horwitz A. F. Tandem events in myoblast fusion. Dev Biol. 1977 Jul 15;58(2):328–338. doi: 10.1016/0012-1606(77)90095-1. [DOI] [PubMed] [Google Scholar]
- Marsh J. B. Lipoproteins in a nonrecirculating perfusate of rat liver. J Lipid Res. 1974 Nov;15(6):544–550. [PubMed] [Google Scholar]
- SINGLETON W. S., GRAY M. S., BROWN M. L., WHITE J. L. CHROMATOGRAPHICALLY HOMOGENEOUS LECITHIN FROM EGG PHOSPHOLIPIDS. J Am Oil Chem Soc. 1965 Jan;42:53–56. doi: 10.1007/BF02558256. [DOI] [PubMed] [Google Scholar]
- Schimmel S. D., Kent C., Bischoff R., Vagelos P. R. Plasma membranes from cultured muscle cells: isolation procedure and separation of putative plasma-membrane marker enzymes. Proc Natl Acad Sci U S A. 1973 Nov;70(11):3195–3199. doi: 10.1073/pnas.70.11.3195. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yaffe D. Developmental changes preceding cell fusion during muscle differentiation in vitro. Exp Cell Res. 1971 May;66(1):33–48. doi: 10.1016/s0014-4827(71)80008-3. [DOI] [PubMed] [Google Scholar]
