Fatty acid binding protein 4 in human skeletal muscle

Biochemical and Biophysical Research Communications

Volumn 346, Issue 1, 2006, Pages 125-130

  Fischer, Heléne ^a   Gustafsson, Thomas ^a   Sundberg, Carl Johan ^a   Norrbom, Jessica ^a   Ekman, Marianne ^a   Johansson, Olle ^a   Jansson, Eva ^a  

^a KAROLINSKA INSTITUTE   (Sweden)

Author keywords

Exercise; FABP3; FABP4; Fat metabolism; Fatty acid binding protein; Gene expression; Immunohistochemistry; Muscle fiber types

Indexed keywords

FATTY ACID BINDING PROTEIN; MESSENGER RNA; PROTEIN SUBUNIT;

ADULT; ARTICLE; CONTROLLED STUDY; ENDURANCE; HUMAN; HUMAN TISSUE; MALE; MUSCLE TISSUE; NORMAL HUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; SKELETAL MUSCLE; TRAINING;

ADOLESCENT; ADULT; FATTY ACID-BINDING PROTEINS; HUMANS; IMMUNOHISTOCHEMISTRY; MALE; MUSCLE, SKELETAL; PHYSICAL FITNESS;

EID: 33745000961     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2006.05.083     Document Type: Article

References (26)

1. Jansson E., and Kaijser L. Substrate utilization and enzymes in skeletal muscle of extremely endurance-trained men. J. Appl. Physiol. 62 (1987) 999-1005
2. Roepstorff C., Halberg N., Hillig T., Saha A.K., Ruderman N.B., Wojtaszewski J.F.P., Richter E.A., and Kiens B. Malonyl-CoA and carnitine in regulation of fat oxidation in human skeletal muscle during exercise. Am. J. Physiol. Endocrinol. Metab. 288 (2005) E133-E142
3. van Loon L.J.C., Koopman R., Stegen J.H.C.H., Wagenmakers A.J.M., Keizer H.A., and Saris W.H.M. Intramyocellular lipids form an important substrate source during moderate intensity exercise in endurance-trained males in a fasted state. J. Physiol. (Lond) 553 (2003) 611-625
4. Rico-Sanz J., Moosavi M., Thomas E.L., McCarthy J., Coutts G.A., Saeed N., and Bell J.D. In vivo evaluation of the effects of continuous exercise on skeletal muscle triglycerides in trained humans. Lipids 35 (2000) 1313-1318
5. Storch J., and Thumser A.E. The fatty acid transport function of fatty acid-binding proteins. Biochim. Biophys. Acta 1486 (2000) 28-44
6. Zimmerman A.W., and Veerkamp J.H. New insights into the structure and function of fatty acid-binding proteins. Cell Mol. Life Sci. 59 (2002) 1096-1116
7. Haunerland N.H., and Spener F. Fatty acid-binding proteins-insights from genetic manipulations. Prog. Lipid Res. 43 (2004) 328-349
8. Glatz J.F., Schaap F.G., Binas B., Bonen A., van der Vusse G.J., and Luiken J.J. Cytoplasmic fatty acid-binding protein facilitates fatty acid utilization by skeletal muscle. Acta Physiol. Scand. 178 (2003) 367-371
9. Binas B., Han X.X., Erol E., Luiken J.J., Glatz J.F., Dyck D.J., Motazavi R., Adihetty P.J., Hood D.A., and Bonen A. A null mutation in H-FABP only partially inhibits skeletal muscle fatty acid metabolism. Am. J. Physiol. Endocrinol. Metab. 285 (2003) E481-E489
10. Bonen A., Luiken J.J.F.P., Arumugam Y., Glatz J.F.C., and Tandon N.N. acute regulation of fatty acid uptake involves the cellular redistribution of fatty acid translocase. J. Biol. Chem. 275 (2000) 14501-14508 10.1074/jbc.275.19.14501
11. Luiken J., Miskovic D., Arumugam Y., Glatz J., and Bonen A. Skeletal muscle fatty acid transport and transporters. Int. J. Sport Nutr. Exerc. Metab. Suppl:S (2001) 92-96
12. Timmons J.A., Larsson O., Jansson E., Fischer H., Gustafsson T., Greenhaff P.L., Ridden J., Rachman J., Peyrard-Janvid M., Wahlestedt C., and Sundberg C.J. Human muscle gene expression responses to endurance training provide a novel perspective on Duchenne muscular dystrophy. Faseb J. 19 (2005) 750-760
13. Coort S.L., Coumans W.A., Bonen A., van der Vusse G.J., Glatz J.F., and Luiken J.J. Divergent effects of rosiglitazone on protein-mediated fatty acid uptake in adipose and in muscle tissues of Zucker rats. J. Lipid Res. 46 (2005) 1295-1302
14. Bergström J. Muscle electrolytes in man. Scand. J. Clin. Lab Invest. 14 (1962) 1-110
15. Chomczynski P., and Sacchi N. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal. Biochem. 162 (1987) 156-159
16. Winer J., Jung C.K.S., Shackel I., and Williams P.M. Development and validation of real-time quantitative reverse transcriptase-polymerase chain reaction for monitoring gene expression in cardiac myocytesin vitro. Anal. Biochem. 270 (1999) 41-49
17. Ameln H., Gustafsson T., Sundberg C.J., Okamoto K., Jansson E., Poellinger L., and Makino Y. Physiological activation of hypoxia inducible factor-1 in human skeletal muscle. Faseb J. 19 (2005) 1009-1011
18. Anderwald C., Bernroider E., Krssak M., Stingl H., Brehm A., Bischof M.G., Nowotny P., Roden M., and Waldhausl W. Effects of insulin treatment in type 2 diabetic patients on intracellular lipid content in liver and skeletal muscle. Diabetes 51 (2002) 3025-3032
19. Pan D.A., Lillioja S., Kriketos A.D., Milner M.R., Baur L.A., Bogardus C., Jenkins A.B., and Storlien L.H. Skeletal muscle triglyceride levels are inversely related to insulin action. Diabetes 46 (1997) 983-988
20. Schmitt B., Fluck M., Decombaz J., Kreis R., Boesch C., Wittwer M., Graber F., Vogt M., Howald H., and Hoppeler H. Transcriptional adaptations of lipid metabolism in tibialis anterior muscle of endurance-trained athletes. Physiol. Genomics 15 (2003) 148-157
21. Qian Q., Kuo L., Yu Y.T., and Rottman J.N. A concise promoter region of the heart fatty acid-binding protein gene dictates tissue-appropriate expression. Circ Res 84 (1999) 276-289
22. Helledie T., Surname F., Jørgensen C., Antonius M., Krogsdam A.-M., Kratchmarova I., Kristiansen K., and Mandrup S. Role of adipocyte lipid-binding protein (ALBP) and acyl-CoA binding protein (ACBP) in PPAR-mediated transactivation. Molecular and Cellular Biochemistry 239 (2002) 157-164
23. McGee S.L., Sparling D., Olson A.-L., and Hargreaves M. Exercise increases MEF2- and GEF DNA-binding activities in human skeletal muscle. Faseb J. 20 (2006) 348-349
24. Koves T.R., Li P., An J., Akimoto T., Slentz D., Ilkayeva O., Dohm G.L., Yan Z., Newgard C.B., and Muoio D.M. Peroxisome Proliferator-activated Receptor-{gamma} Co-activator 1{alpha}-mediated Metabolic Remodeling of Skeletal Myocytes Mimics Exercise Training and Reverses Lipid-induced Mitochondrial Inefficiency 10.1074/jbc.M507621200. J. Biol. Chem. 280 (2005) 33588-33598
25. Makowski L., and Hotamisligil G.S. Fatty acid binding proteins-the evolutionary crossroads of inflammatory and metabolic responses. J. Nutr. 134 (2004) 2464S-2468S
26. Tunstall R.J., Mehan K.A., Wadley G.D., Collier G.R., Bonen A., Hargreaves M., and Cameron-Smith D. Exercise training increases lipid metabolism gene expression in human skeletal muscle. Am. J. Physiol. Endocrinol. Metab. 283 (2002) E66-E72