Muscle fiber type specificity in insulin signal transduction

American Journal of Physiology - Regulatory Integrative and Comparative Physiology

Volumn 277, Issue 6 46-6, 1999, Pages

  Song, Xiao Mei ^b   Ryder, Jeffrey W ^b   Kawano, Yuichi ^b   Chibalin, Alexander V ^b   Krook, Anna ^b   Zierath, Juleen R ^a  

^a KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

^b NONE

Author keywords

Akt kinase; Insulin receptor; Insulin receptor substrate; Phosphatidylinositol 3 kinase

Indexed keywords

INSULIN; INSULIN RECEPTOR; INSULIN RECEPTOR SUBSTRATE 1; INSULIN RECEPTOR SUBSTRATE 2; PHOSPHATIDYLINOSITOL 3 KINASE;

ANIMAL TISSUE; ARTICLE; ENZYME ACTIVITY; EXTENSOR DIGITORUM LONGUS MUSCLE; MALE; MUSCLE CELL; NONHUMAN; OXIDATIVE PHOSPHORYLATION; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN PHOSPHORYLATION; RAT; SIGNAL TRANSDUCTION; SOLEUS MUSCLE;

EID: 0010164060     PISSN: 03636119     EISSN: None     Source Type: Journal    
DOI: 10.1152/ajpregu.1999.277.6.r1690     Document Type: Article

References (36)

1. Ariano, M. A., R. B. Armstrong, and V. R. Edgerton. Hindlimb muscle fiber population of five animals. J. Histochem. 21: 51-55, 1973.
2. Björnholm, M., Y. Kawano, M. Lehtihet, and J. R. Zierath. Insulin receptor substrate-phosphorylation and phosphatidylinositol 3-kinase activity in skeletal muscle from NIDDM subjects after in vivo insulin stimulation. Diabetes 46: 524-427, 1997.
3. Bonen, A., M. H. Tan, and W. M. Watson-Wright. Insulin binding and glucose uptake differences in rodent skeletal muscles. Diabetes 30: 702-704, 1981.
4. Deems, R. O., J. L. Evans, R. W. Deacon, C. M. Honer, D. T. Chu, K. Bürki, W. S. Fillers, D. K. Cohen, and D. A. Young, Expression of human GLUT4 in mice results in increased insulin action. Diabetologia 37: 1097-1104, 1994.
5. DeFronzo, R. A., R. Gunnarsson, O. Björkman, M. Olsson, and J. Wahren. Effects of insulin on peripheral and splanchnic glucose metabolism in non-insulin-dependent (Type II) diabetes mellitus. J. Clin. Invest. 76: 149-155, 1985.
6. DeFronzo, R.A., E. Jacot, E. Jequier, E. Maeder, J. Wahren, and J. P. Felber. The effect of insulin on the disposal of intravenous glucose. Results from indirect calorimetry and hepatic and femoral venous catheterization. Diabetes 30: 1000-1007, 1981.
7. Essén, B., E. Jansson, J. Henriksson, A. W. Taylor, and B. Saltin. Metabolic characteristics of fiber types in human skeletal muscle. Acta Physiol. Scand. 95: 153-165, 1975.
8. Hajduch, E., D. R. Alessi, B. A. Hemmings, and H. S. Hundal. Constitutive activation of protein kinase Bα by membrane targeting promotes glucose and system A amino acid transport, protein synthesis, and inactivation of glycogen synthase kinase 3 in L6 muscle cells. Diabetes 47: 1006-1013, 1998.
9. Hansen, P., E. Gulve, B. Marshall, J. Gao, J. Pessin, J. O. Holloszy, and M. Mueckler. Skeletal muscle glucose transport and metabolism are enhanced in transgenic mice overexpressing the GLUT4 glucose transporter. J. Biol. Chem. 270: 1679-1684, 1995.
10. Henriksen, E. J., R. E. Bourey, K. J. Rodnick, L. Koranyi, M. A. Permutt, and J. O. Holloszy. Glucose transporter protein content and glucose transport capacity in rat skeletal muscle. Am. J. Physiol. 259 (Endocrinol. Metab. 22): E593-E598, 1990.
11. Henriksen, E. J., and J. O. Holloszy. Effect of diffusion distance on measurement of rat skeletal muscle glucose transport in vitro. Acta Physiol. Scand. 143: 381-386, 1991.
12. Heydrick, S. J., D. Jullien, N. Gautier, J.-F. Tanti, S. Giorgetti, E. Van Obberghen, and Y. Marchand-Brustel. Defect in skeletal muscle phosphatidylinositol-3-kinase in obese insulin-resistant mice. J. Clin. Invest. 91: 1358-1366, 1993.
13. Hickey, M. S., J. O. Carey, J. L. Azevedo, J. A. Houmard, W. J. Pories, R. G. Israel, and G. L. Dohm. Skeletal muscle fiber composition is related to adiposity and in vitro glucose transport rate in humans. Am. J. Physiol. 268 (Endocrinol. Metab. 31): E453-E457, 1995.
14. Hjeltnes, N., D. Galuska, M. Björnholm, A.-K. Aksnes, A. Lannem, J. R. Zierath, and H. Wallberg-Henriksson. Exercise-induced overexpression of key regulatory proteins involved in glucose uptake and metabolism in tetraplegic persons: molecular mechanisms for improved glucose homeostasis. FASEB J. 12: 1701-1712, 1998.
15. James, D. E., A. B. Jenkins, and E. W. Kraegen. Heterogeneity of insulin action in individual muscles in vivo: euglycemic clamp studies in rats. Am. J. Physiol. 248 (Endocrinol. Metab. 11): E567-E574, 1985.
16. James, D. E., A. Zorzano, M. Böni-Schnetzler, R. A. Nemenoff, A. Powers, P. F. Pilch, and N. B. Ruderman. Intrinsic differences of insulin receptor kinase activity in red and white muscle. J. Biol. Chem. 261: 14939-14944, 1986.
17. Kern, M., J. A. Wells, J. M. Stephens, C. W. Elton, J. E. Friedman, E. B. Tapscott, P. H. Pekala, and G. L. Dohn. Insulin responsiveness in skeletal muscle is determined by glucose transporter (GLUT4) protein level. Biochem. J. 270: 397-400, 1990.
18. Kohn, A. D., S. A. Summers, M. J. Birnbaum, and R. A. Roth. Expression of constitutively active AKT Ser/Ser kinase in 3T3-L1 adipocytes stimulates glucose uptake and glucose transporter 4 translocation. J. Biol. Chem. 271: 31372-31378, 1996.
19. Kriketos, A. D., D. A. Pan, S. Lillioja, G. J. Cooney, L. A. Baur, M. R. Milner, J. R. Sutton, A. B. Jenkins, C. Bogardus, and L. H. Storlien. Interrelationships between muscle morphology, insulin action, and adiposity. Am. J. Physiol. 270 (Regulatory Integrative Comp. Physiol. 39): R1332-R1339, 1996.
20. Krook, A., R. A. Roth, X. J. Jiang, J. R. Zierath, and H. Wallberg-Henriksson. Insulin-stimulated Akt kinase activity is reduced in skeletal muscle from non-insulin-dependent diabetic subjects. Diabetes 47: 1281-1286, 1998.
21. Krook, A., J. P. Whitehead, S. P. Dobson, M. R. Griffiths, M. Ouwents, C. Baker, A. C. Hayward, S. K. Sen, J. A. Maassen, K. Siddle, J. M. Tavare, and S. O'Rahilly. Two naturally occurring insulin receptor tyrosine kinase domain mutants provide evidence that phosphoinositide 3-kinase activation alone is not sufficient for the mediation of insulin's metabolic and mitogenic effects. J. Biol. Chem. 272: 30208-30214, 1997.
22. Lillioja, S., A. A. Young, C. L. Culter, J. L. Ivy, G. H. Abbott, J. K. Zawadzki, H. Yki-Järvinen, L. Christin, T. W. Secomb, and C. Bogardus. Skeletal muscle capillary density and fiber type are possible determinants of in vivo insulin resistance in man. J. Clin. Invest. 80: 415-424, 1987.
23. Lithell, H., F. Lindegärde, K. Hellsing, G. Lundquist, E. Nygaard, and B. Saltin. Body weight, skeletal muscle morphology, and enzyme activities in relation to fasting serum insulin concentration and glucose tolerance in 48-year-old men. Diabetes 30: 19-25, 1981.
24. Lowry, C. V., J. S. Kimmey, S. Felder, M.-Y. Chi, K. K. Kaiser, P. N. Passonneau, K. A. Kirk, and O. H. Lowry. Enzyme patterns in single human muscle fibers. J. Biol. Chem. 253: 8269-8277, 1978.
25. Marshall, B. A., and M. M. Mueckler. Differential effects of GLUT-1 or GLUT-4 overexpression on insulin responsiveness in transgenic mice. Am. J. Physiol. 267 (Endocrinol. Metab. 30): E738-E744, 1994.
26. Megeney, L. A., P. D. Neufer, G. L. Dohm, M. H. Tan, C. A. Blewett, G. C. B. Elder, and A. Bonen. Effects of muscle activity and fiber composition on glucose transport and GLUT-4. Am. J. Physiol. 264 (Endocrinol. Metab. 27): E583-E593, 1993.
27. Nyholm, B., Z. Qu, A. Kaal, S. Bønnelykke Pedersen, C. Højbjerg Gravholt, J. Løvind Andersen, B. Saltin, and O. Schmitz. Evidence of an increased number of Type IIb muscle fibers in insulin-resistant first-degree relatives of patients with NIDDM. Diabetes 46: 1822-1828, 1997.
28. Ogawa, W., T. Matozaki, and M. Kasuga. Role of binding proteins to IRS-1 in insulin signaling. Mol. Cell. Biochem. 182: 13-22, 1998.
29. Saltin, B., and P. D. Gollnick. Skeletal muscle adaptability: significance for metabolism and performance. In: Handbook of Physiology. Skelatal Muscle. Bethesda, MD: Am. Physiol. Soc., 1983, sect. 10, chapt. 19, p. 555-631.
30. Song, X.-M., Y. Kawano, A. Krook, J. W. Ryder, S. Efendic, R. A. Roth, H. Wallberg-Henriksson, and J. R. Zierath. Muscle fiber type-specific defect in insulin signal transduction to glucose transport in diabetic GK rats. Diabetes 48: 664-670, 1999.
31. Tanti, J. F., S. Grillo, T. Greméaux, P. J. Coffer, E. Van Obberghen, and Y. Le Marchand-Brustel. Potential role of protein kinase B in glucose transporter 4 translocation in adipocytes. Endocrinology 138: 2005-2010, 1997.
32. Turinsky, J., and A. Damrau-Abney. Akt kinases and 2-deoxy-glucose uptake in rat skeletal muscles in vivo: study with insulin and exercise. Am. J. Physiol. 276 (Regulatory Integrative Comp. Physiol. 45): R277-R282, 1999.
33. Wallberg-Henriksson, H. Glucose transport in to skeletal muscle: influence of contractile activity, insulin, catecholamines and diabetes mellitus. Acta Physiol. Scand. 131, Suppl. 564: 1-80, 1987.
34. White, M. F. The IRS-1 signaling system: a network of docking proteins that mediate insulin action. Mol. Cell. Biochem. 182: 3-11, 1998.
35. Withers, D. J., J. Sanchez Gutierrez, H. Towery, D. J. Burks, J.-M. Ren, S. Previs, Y. Zhang, D. Bernal, S. Pons, G. I. Schulman, S. Bonner-Weir, and M. F. White. Disruption of IRS-2 causes type 2 diabetes in mice. Nature 391: 900-904, 1998.
36. Zierath, J. R., L. He, A. Gumà, E. Odegaard Wahlström, A. Klip, and H. Wallberg-Henriksson. Insulin action on glucose transport and plasma membrane GLUT4 content in skeletal muscle from patients with NIDDM. Diabetologia 39: 1180-1189, 1996.