Musclin gene expression is strongly related to fast-glycolytic phenotype

Biochemical and Biophysical Research Communications

Volumn 353, Issue 3, 2007, Pages 713-718

  Banzet, S ^a   Koulmann, N ^a   Sanchez, H ^a   Serrurier, B ^a   Peinnequin, A ^a   Bigard, A X ^a  

^a CENTRE DE RECHERCHES   (France)

Author keywords

Fiber type; Insulin resistance; Myokine; Osteocrin; Skeletal muscle

Indexed keywords

INSULIN; MESSENGER RNA; MUSCLE PROTEIN; MUSCLIN; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; GASTROCNEMIUS MUSCLE; GENE EXPRESSION; GENETIC TRANSCRIPTION; GLYCOLYSIS; INSULIN RESISTANCE; INSULIN SENSITIVITY; MUSCLE CELL; MUSCLE TWITCH; NONHUMAN; NUCLEOTIDE SEQUENCE; PHENOTYPE; PLANTARIS MUSCLE; PRIORITY JOURNAL; RAT; SOLEUS MUSCLE;

ANIMALS; GENE EXPRESSION; GLYCOLYSIS; HINDLIMB SUSPENSION; MUSCLE FIBERS, FAST-TWITCH; MUSCLE FIBERS, SLOW-TWITCH; MUSCLE PROTEINS; MUSCLE, SKELETAL; MYOSIN HEAVY CHAINS; PHENOTYPE; RATS; RATS, WISTAR;

EID: 33846019968     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2006.12.074     Document Type: Article

References (30)

1. Febbraio M.A., Hiscock N., Sacchetti M., Fischer C.P., and Pedersen B.K. Interleukin-6 is a novel factor mediating glucose homeostasis during skeletal muscle contraction. Diabetes 53 (2004) 1643-1648
2. van Hall G., Steensberg A., Sacchetti M., Fischer C., Keller C., Schjerling P., Hiscock N., Moller K., Saltin B., Febbraio M.A., and Pedersen B.K. Interleukin-6 stimulates lipolysis and fat oxidation in humans. J. Clin. Endocrinol. Metab. 88 (2003) 3005-3010
3. Akerstrom T., Steensberg A., Keller P., Keller C., Penkowa M., and Pedersen B.K. Exercise induces interleukin-8 expression in human skeletal muscle. J. Physiol. 563 (2005) 507-516
4. Pedersen B.K., Steensberg A., Fischer C., Keller C., Keller P., Plomgaard P., Wolsk-Petersen E., and Febbraio M. The metabolic role of IL-6 produced during exercise: is IL-6 an exercise factor?. Proc. Nutr. Soc. 63 (2004) 263-267
5. Nishizawa H., Matsuda M., Yamada Y., Kawai K., Suzuki E., Makishima M., Kitamura T., and Shimomura I. Musclin, a novel skeletal muscle-derived secretory factor. J. Biol. Chem. 279 (2004) 19391-19395
6. Thomas G., Moffatt P., Salois P., Gaumond M.H., Gingras R., Godin E., Miao D., Goltzman D., and Lanctot C. Osteocrin, a novel bone-specific secreted protein that modulates the osteoblast phenotype. J. Biol. Chem. 278 (2003) 50563-50571
7. James D.E., Jenkins A.B., and Kraegen E.W. Heterogeneity of insulin action in individual muscles in vivo: euglycemic clamp studies in rats. Am. J. Physiol. 248 (1985) E567-E574
8. Bonen A., Tan M.H., and Watson-Wright W.M. Insulin binding and glucose uptake differences in rodent skeletal muscles. Diabetes 30 (1981) 702-704
9. Kern M., Wells J.A., Stephens J.M., Elton C.W., Friedman J.E., Tapscott E.B., Pekala P.H., and Dohm G.L. Insulin responsiveness in skeletal muscle is determined by glucose transporter (Glut4) protein level. Biochem. J. 270 (1990) 397-400
10. Song X.M., Ryder J.W., Kawano Y., Chibalin A.V., Krook A., and Zierath J.R. Muscle fiber type specificity in insulin signal transduction. Am. J. Physiol. 277 (1999) R1690-R1696
11. Fluck M., and Hoppeler H. Molecular basis of skeletal muscle plasticity-from gene to form and function. Rev. Physiol. Biochem. Pharmacol. 146 (2003) 159-216
12. Schiaffino S., and Reggiani C. Molecular diversity of myofibrillar proteins: gene regulation and functional significance. Physiol. Rev. 76 (1996) 371-423
13. Fitts R.H., Metzger J.M., Riley D.A., and Unsworth B.R. Models of disuse: a comparison of hindlimb suspension and immobilization. J. Appl. Physiol. 60 (1986) 1946-1953
14. Bigard A.X., Zoll J., Ribera F., Mateo P., Sanchez H., Serrurier B., and Ventura-Clapier R. Influence of overload on phenotypic remodeling in regenerated skeletal muscle. Am. J. Physiol. Cell Physiol. 281 (2001) C1686-C1694
15. Birot O.J., Koulmann N., Peinnequin A., and Bigard X.A. Exercise-induced expression of vascular endothelial growth factor mRNA in rat skeletal muscle is dependent on fibre type. J. Physiol. 552 (2003) 213-221
16. Banzet S., Koulmann N., Simler N., Birot O., Sanchez H., Chapot R., Peinnequin A., and Bigard X. Fibre-type specificity of interleukin-6 gene transcription during muscle contraction in rat: association with calcineurin activity. J. Physiol. 566 (2005) 839-847
17. Livak K.J., and Schmittgen T.D. Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method. Methods 25 (2001) 402-408
18. Vandesompele J., De Preter K., Pattyn F., Poppe B., Van Roy N., De Paepe A., and Speleman F. Accurate normalization of real-time quantitative RT-PCR data by geometric averaging of multiple internal control genes. Genome Biol. 3 (2002) RESEARCH0034
19. Staiger H., Haas C., Machicao F., and Haring H.U. The PPARgamma agonist troglitazone induces musclin mRNA expression in human myotubes. Horm. Metab. Res. 38 (2006) 614-616
20. Kawamura T., Yoshida K., Sugawara A., Nagasaka M., Mori N., Takeuchi K., and Kohzuki M. Regulation of skeletal muscle peroxisome proliferator-activated receptor gamma expression by exercise and angiotensin-converting enzyme inhibition in fructose-fed hypertensive rats. Hypertens. Res. 27 (2004) 61-70
21. Baldwin K.M., and Haddad F. Effects of different activity and inactivity paradigms on myosin heavy chain gene expression in striated muscle. J. Appl. Physiol. 90 (2001) 345-357
22. Bigard A.X., Boehm E., Veksler V., Mateo P., Anflous K., and Ventura-Clapier R. Muscle unloading induces slow to fast transitions in myofibrillar but not mitochondrial properties. Relevance to skeletal muscle abnormalities in heart failure. J. Mol. Cell Cardiol. 30 (1998) 2391-2401
23. Gaster M., Staehr P., Beck-Nielsen H., Schroder H.D., and Handberg A. GLUT4 is reduced in slow muscle fibers of type 2 diabetic patients: is insulin resistance in type 2 diabetes a slow, type 1 fiber disease?. Diabetes 50 (2001) 1324-1329
24. He J., Watkins S., and Kelley D.E. Skeletal muscle lipid content and oxidative enzyme activity in relation to muscle fiber type in type 2 diabetes and obesity. Diabetes 50 (2001) 817-823
25. Marette A., Burdett E., Douen A., Vranic M., and Klip A. Insulin induces the translocation of GLUT4 from a unique intracellular organelle to transverse tubules in rat skeletal muscle. Diabetes 41 (1992) 1562-1569
26. Megeney L.A., Neufer P.D., Dohm G.L., Tan M.H., Blewett C.A., Elder G.C., and Bonen A. Effects of muscle activity and fiber composition on glucose transport and GLUT-4. Am. J. Physiol. 264 (1993) E583-E593
27. Geiger P.C., Han D.H., Wright D.C., and Holloszy J.O. How muscle insulin sensitivity is regulated: testing of a hypothesis. Am. J. Physiol. Endocrinol. Metab. 291 (2006) E1258-E1263
28. Marin P., Andersson B., Krotkiewski M., and Bjorntorp P. Muscle fiber composition and capillary density in women and men with NIDDM. Diabetes Care 17 (1994) 382-386
29. Lillioja S., Young A.A., Culter C.L., Ivy J.L., Abbott W.G., Zawadzki J.K., Yki-Jarvinen H., Christin L., Secomb T.W., and Bogardus C. Skeletal muscle capillary density and fiber type are possible determinants of in vivo insulin resistance in man. J. Clin. Invest. 80 (1987) 415-424
30. Tanner C.J., Barakat H.A., Dohm G.L., Pories W.J., MacDonald K.G., Cunningham P.R., Swanson M.S., and Houmard J.A. Muscle fiber type is associated with obesity and weight loss. Am. J. Physiol. Endocrinol. Metab. 282 (2002) E1191-E1196