A new procedure for the isolation of plasma membranes, T tubules, and internal membranes from skeletal muscle

American Journal of Physiology - Endocrinology and Metabolism

Volumn 270, Issue 4 33-4, 1996, Pages

  Dombrowski, Luce ^a   Roy, Denis ^a   Marcotte, Bruno ^a   Marette, Andre ^a  

^a UNIVERSITÉ LAVAL   (Canada)

Author keywords

calcium adenosinetriphosphatase; dihydropyridine receptor; GLUT 1; ryanodine receptor; sarcoplasmic reticulum; transverse tubules; 1 sodium potassium adenosinetriphosphatase

Indexed keywords

ADENOSINE TRIPHOSPHATASE (CALCIUM); ADENOSINE TRIPHOSPHATASE (POTASSIUM SODIUM); GLUCOSE TRANSPORTER; INSULIN; RYANODINE RECEPTOR;

ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CELL FRACTIONATION; CONTROLLED STUDY; DIABETES MELLITUS; GLUCOSE TRANSPORT; MALE; MEMBRANE MARKER; MUSCLE FIBER MEMBRANE; NONHUMAN; PRIORITY JOURNAL; PROTEIN CONTENT; RAT; SARCOPLASMIC RETICULUM; TRANSVERSE TUBULAR SYSTEM;

EID: 0029925423     PISSN: 01931849     EISSN: None     Source Type: Journal    
DOI: 10.1152/ajpendo.1996.270.4.e667     Document Type: Article

References (30)

1. Bers, D. M., K. D. Philipson, and A. Y. Nishimoto. Sodium-calcium exchange and sidedness of isolated cardiac sarcolemmal vesicles. Biochim. Biophys. Acta 601: 358-371, 1980.
2. Bornemann, A., T. Ploug, and H. Schmalbruch. Subcellular localization of Glut4 in nonstimulated and insulin-stimulated soleus muscle of rat. Diabetes 41: 215-221, 1992.
3. Brandt, N. R., A. H. Caswell, S.-R. Wen, and J. A. Talvenheimo. Molecular interactions of the junctional foot protein and dihydropyridine receptor in skeletal muscle triads. J. Membr. Biol. 113: 237-251, 1990.
4. Brozinick, J. T., G. J. Etgen, B. B. Yaspelkis III, and J. L. Ivy. The effects of muscle contraction and insulin on glucose-transporter translocation in rat skeletal muscle. Biochem. J. 297: 539-545, 1994.
5. Brozinick, J. T., Jr., G. J. Etgen, Jr., B. B. Yaspelkis III, and J. L. Ivy. Glucose uptake and GLUT-4 protein distribution in skeletal muscle of the obese Zucker rat. Am. J. Physiol. 267 (Regulatory Integrative Comp. Physiol. 36): R236-R243, 1994.
6. Cullen, M. J., S. Hollingworth, and M. W. Marshall. A comparative study of the transverse tubular system of the rat extensor digitorum longus and soleus muscles. J. Anat. 138: 297-308, 1984.
7. Doucet, J.-P., and B. S. T. Tuana. Identification of low molecular weight GTP-binding proteins and their sites of interaction in subcellular fractions from skeletal muscle. J. Biol. Chem. 266: 17613-17620, 1991.
8. Douen, A. G., E. Burdett, T. Ramlal, S. Rastogi, M. Vranic, and A. Klip. Characterization of glucose transporter-enriched membranes from rat skeletal muscle: assessment of endothelial cell contamination and presence of sarcoplasmic reticulum and transverse tubules. Endocrinology 128: 611-616, 1991.
9. 3H)BMPA photolabel. FEBS Lett. 339: 205-208, 1994.
10. Eisenberg, B. R. Quantitative ultrastructure of mammalian skeletal muscle. In: Handbook of Physiology. Skeletal Muscle. Bethesda, MD: Am. Physiol. Soc., 1983, sect. 10, chapt. 3, p. 73-112.
11. Eisenberg, B. R., and A. M. Kuda. Discrimination between fiber population in mammalian skeletal muscle by using ultrastructural parameters. J. Ultrastruct. Res. 54: 76-88, 1976.
12. Etgen, G. J., A. R. Memon, G. A. Thompson, and J. L. Ivy. Insulin- and contraction-stimulated translocation of GTP-binding proteins and GLUT4 protein in skeletal muscle. J. Biol. Chem. 268: 20164-20169, 1993.
13. Franzini-Armstrong, C. The anatomy, physiology, and biochemistry of muscle. The sarcoplasmic reticulum and the transverse tubules. In: Myology, edited by A. G. E. B. Q. Banker. New York: McGraw-Hill, 1986, p. 125-154.
14. Franzini-Armstrong, C., D. G. Ferguson, and C. Champ. Discrimination between fast- and slow-twitch fibres of guinea pig skeletal muscle using the relative surface density of junctional transverse tubule membrane. J. Muscle Res. Cell Motil. 9: 403-414, 1988.
15. Friedman, J. E., R. W. Dudek, D. S. Whitehead, D. L. Downes, W. R. Frisell, J. F. Caro, and L. Dohm. Immunolocalization of glucose transporter GLUT4 within human skeletal muscle. Diabetes 40: 150-154, 1991.
16. Friedman, J. E., W. H. Sherman, M. J. Reed, C. W. Elton, and G. L. Dohm. Exercise training increases glucose transporter protein GLUT-4 in skeletal muscle of obese Zucker (fa/fa) rats. FEBS Lett. 268: 13-16, 1990.
17. Goodyear, L. J., M. F. Hirshman, and E. S. Horton. Exercise-induced translocation of skeletal muscle glucose transporters. Am. J. Physiol. 261 (Endocrinol. Metab. 24): E795-E799, 1991.
18. Hirshman, M. F., L. J. Goodyear, L. J. Wardzala, E. D. Horton, and E. S. Horton. Identification of an intracellular pool of glucose transporters from basal and insulin-stimulated rat skeletal muscle. J. Biol. Chem. 265: 987-991, 1990.
19. Hundal, H. S., A. Marette, Y. Mitsumoto, T. Ramlal, R. Blostein, and A. Klip. Insulin induces translocation of the α2 and β1 subunits of the Na+/K+-ATPase from intracellular compartments to the plasma membrane in mammalian skeletal muscle. J. Biol. Chem. 267: 5040-5043, 1992.
20. Kim, C. K., A. H. Caswell, J. A. Talvenheimo, and N. R. Brandt. Isolation of a terminal cisternae protein which may link the dihydropyridine receptor to the junctional foot protein in skeletal muscle. Biochemistry 29: 9281-9289, 1990.
21. Klip, A., and A. Marette. Acute and chronic signals controlling glucose transport in skeletal muscle. J. Cell. Biochem. 48: 51-60, 1992.
22. Klip, A., T. Ramlal, A. G. Douen, E. Burdett, D. Young, G. D. Cartee, and J. O. Holloszy. Insulin-induced decrease in 5′-nucleotidase activity in skeletal muscle membranes. FEBS Lett. 238: 419-423, 1988.
23. Klip, A., T. Ramlal, D. A. Young, and J. O. Holloszy. Insulin induced translocation of glucose transporters in rat hindlimb muscles. FEBS Lett. 224: 224-230, 1987.
24. Laemmli, U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature Lond. 227: 680-635, 1970.
25. Marette, A., E. Burdett, A. Douen, M. Vranic, and A. Klip. Insulin induces the translocation of GLUT4 from a unique intracellular organelle to transverse tubules in rat skeletal muscle. Diabetes 41: 1562-1569, 1992.
26. +-ATPase α2-subunit in the surface of rat skeletal muscle-morphological evidence. Am. J. Physiol. 265 (Cell Physiol. 34): C1716-C1722, 1993.
27. Marette, A., J. M. Richardson, T. Ramlal, T. W. Balon, M. Vranic, J. E. Pessin, and A. Klip. Abundance, localization, and insulin-induced translocation of glucose transporters in red and white muscle. Am. J. Physiol. 263 (Cell Physiol. 32): C443-C452, 1992.
28. Rodnick, K. J., J. W. Slot, D. R. Studelska, D. E. Hanpeter, L. J. Robinson, H. J. Geuze, and D. E. James. Immunucytochemical and biochemical studies of GLUT4 in rat skeletal muscle. J. Biol. Chem. 267: 6278-6285, 1992.
29. Slot, J. W., H. J. Geuze, S. Gigendack, D. E. James, and G. E. Lienhard. Translocation of the glucose transporter GLUT4 in cardiac myocytes of the rat. Proc. Natl. Acad. Sci. USA 88: 7815-7819, 1991.
30. Song, C. S., and O. Bodansky. Subcellular localization and properties of 5′-nucleotidase in the rat liver. J. Biol. Chem. 242: 694-699, 1967.