Expression of the extracellular fatty acid binding protein (Ex-FABP) during muscle fiber formation in vivo and in vitro

Experimental Cell Research

Volumn 242, Issue 2, 1998, Pages 410-418

  Gentili, Chiara ^a   Cermelli, Silvia ^a   Tacchetti, Carlo ^b   Cossu, Giulio ^c   Cancedda, Ranieri ^a,b   Cancedda, Fiorella Descalzi ^a,d  

^a CENTRO DI BIOTECNOLOGIE AVANZATE   (Italy)

^b UNIVERSITY OF GENOA   (Italy)

^c SAPIENZA UNIVERSITY OF ROME   (Italy)

^d CNR   (Italy)

Author keywords

Fatty acid; Lipocalin; Myogenesis

Indexed keywords

FATTY ACID BINDING PROTEIN; MESSENGER RNA;

ANIMAL CELL; ARTICLE; CHICK EMBRYO; EMBRYO; EMBRYO DEVELOPMENT; IMMUNOFLUORESCENCE; IMMUNOHISTOCHEMISTRY; IN SITU HYBRIDIZATION; MUSCLE DEVELOPMENT; MYOTUBE; NONHUMAN; PRIORITY JOURNAL; PROTEIN DETERMINATION; PROTEIN EXPRESSION;

ANIMALIA; GALLUS GALLUS;

EID: 0032146101     PISSN: 00144827     EISSN: None     Source Type: Journal    
DOI: 10.1006/excr.1998.4098     Document Type: Article

References (39)

1. Börchers T., Spener F. Fatty acid binding proteins. Curr. Top. Membr. 40:1994;261-294.
2. Watanabe R., Fujii H., Odani S., Sakakibara J., Yamamoto A., Ito M., Ono T. Molecular cloning of a cDNA encoding a novel fatty acid-binding protein from rat skin. Biochem. Biophys. Res. Commun. 200:1994;253-259.
3. Schmitt M. C., Jamison R. S., Orgebin-Crist M. C., Ong D. E. A novel, testis-specific member of the cellular ipophilic transport protein superfamily, deduced from a complementary deoxyribonucleic acid clone. Biol. Reprod. 51:1994;239-245.
4. Feng L., Hatten M. E., Heintz N. Brain lipid-binding protein (BLBP): A novel signaling system in the developing mammalian CNS. Neuron. 12:1994;895-908.
5. Kurtz A., Zimmer A., Schnütgen F., Brüning G., Spener F., Müller T. The expression pattern of a novel gene encoding brain-fatty acid binding protein correlates with neuronal and glial cell development. Development. 120:1994;2637-2649.
6. Matarese V., Stone R. L., Waggoner D. W., Bernlohr D. A. Intracellular fatty acid trafficking and the role of cytosolic lipid binding proteins. Prog. Lipid Res. 28:1989;245-272.
7. Nielson S. U., Spener F. Fatty acid-binding protein from rat heart is phosphorylated on Tyr 19 in response to insulin stimulation. J. Lipid Res. 34:1993;1355-1366.
8. Nielson S. U., Rump R., Hojrup P., Roepstrorff P., Spener F. Differentiational regulation and phosphorylation of the fatty acid-binding protein from rat mammary epithelial cells. Biochim. Biophys. Acta. 1211:1994;189-197.
9. Yang Y., Spitzer E., Kenney N., Zschiesche W., Li M., Kromminga A., Müller T., Spener F., Lezius A., Veerkamp J. H., Smith G. H., Solomon D. S., Grosse R. Members of the fatty acid-binding protein family are differentiation factors for the mammary gland. J. Cell Biol. 127:1994;1097-1109.
10. Börchers T., Unteberg C., Rüdel H., Robenek H., Spener F. Subcellular distribution of cardiac fatty acid-binding protein in bovine heart muscle and quantitation with an enzyme-linked immunosorbent assay. Biochim. Biophys. Acta. 1002:1989;54-61.
11. Crisman T. S., Claffey K. P., Saouaf R., Hanspai J., Brecher P. Measurement of rat heart fatty acid binding protein by ELISA. Tissue distribution, developmental changes and subcellular distribution. J. Mol. Cell. Cardiol. 19:1987;423-431.
12. Paulussen R. J., Geelen M. J., Beynen A. C., Veerkamp J. H. Immunochemical quantitation of fatty acid binding proteins. Tissue and intracellular distribution, postnatal development and influence of physiological conditions on rat heart and liver FABP. Biochim. Biophys. Acta. 1001:1989;201-209.
13. Peeters R. A., in't-Groen M. A., Veerkamp J. H. The fatty acid binding protein from human skeletal muscle. Arch. Biochem. Biophys. 274:1989;556-563.
14. Felig P., Wahren J. Fuel homeostasis in exercise. N. Engl. J. Med. 293:1975;1078-1084.
15. Lopaschuk G. D., Saddik M. The relative contribution of glucose and fatty acids to ATP production in hearts reperfused following ischemia. Mol. Cell. Biochem. 116:1992;111-116.
16. Descalzi Cancedda F., Malpeli M., Gentili C., Di Marzo V., Bet P., Carlevaro M., Cermelli S., Cancedda R. The developmentally regulated avian Ch21 lipocalin is an extracelular fatty acid-binding protein. J. Biol. Chem. 271:1996;20163-20169.
17. Descalzi Cancedda F., Manduca P., Tacchetti C., Fossa P., Quarto R., Cancedda R. Developmentally regulated synthesis of a low molecular weight protein (Ch 21) by differentiating chondrocytes. J. Cell Biol. 107:1988;2455-2463.
18. Manduca P., Descalzi Cancedda F., Tacchetti C., Quarto R., Fossa P., Cancedda R. Synthesis and secretion of Ch 21 protein in embryonic chick skeletal tissues. Eur. J. Cell Biol. 50:1989;154-161.
19. Descalzi Cancedda F., Dozin B., Rossi F., Molina F., Cancedda R., Negri A., Ronchi S. The Ch 21 protein, developmentally regulated in chick embryo, belongs to the superfamily of lipophilic molecule carrier proteins. J. Biol. Chem. 265:1990;19060-19064.
20. Dozin B., Descalzi F., Briata P., Hayashy M., Gentili C., Hayashi K., Quarto R., Cancedda R. Expression, regulation, and tissue distribution of the Ch 21 protein during chicken embryogenesis. J. Biol. Chem. 267:1992;2979-2985.
21. Ferrari S., Battini R., Cossu G. Differentiation dependant expression of Apolipoprotein AI in chicken myogenic cells in culture. Dev. Biol. 140:1990;430-436.
22. Edgell C. J. S., McDonald C. C., Graham J. B. Permanent cell line expressing human factor VIII-related antigen established by hybridization. Proc. Natl. Acad. Sci. USA. 80:1983;3734-3737.
23. Tajbakhsh S., Vivarelli E., Cusella De Angelis G., Rocancourt D., Buckingham M., Cossu G. A population of myogenic cells derived from the mouse neural tube. Neuron. 13:1994;813-821.
24. Chomczynski P., Sacchi N. Single-step method of RNA isolation by acid guanidium thycyanate-phenol-chloroform extraction. Anal. Biochem. 162:1987;156-159.
25. Krystosek A., Cawthon M. L., Kabat D. Improved methods for purification and assay of eukariotic messenger ribonucleic acids and ribosomes. Quantitative analysis of their interaction in a fractionated reticulocyte cell-free system. J. Biol. Chem. 250:1975;6077-6084.
26. Carey J. O., Neufer P. D., Farrar R. P., Veerkamp J. H., Dohm G. L. Transcriptional regulation of muscle fatty acid-binding protein. Biochem. J. 298:1994;613-617.
27. Rump R., Buhlmann C., Börchers T., Spener F. Differentiation-dependent expression of heart type fatty acid-binding protein in C2C12 muscle cells. Eur. J. Cell Biol. 69:1996;135-142.
28. Veerkamp J. H., van Moerkerk H. T. Fatty acid-binding protein and its relation to fatty acid oxidation. Mol. Cell Biochem. 123:1993;101-106.
29. Glatz J. F. C., Vork M. N., Cistola D. P., van der Vusse G. J. Cytoplasmic fatty acid binding protein: Significance for intracellular transport of fatty acids and putative role on signal transduction pathways. Prostaglandins Leukotrienes Essent. Fatty Acids. 48:1993;33-41.
30. Sauro V. S., Strickland K. P. Changes in oleic acid oxidation and incorporation into lipids of differentiating L6 myoblasts cultured in normal or fatty acid-supplemented growth medium. Biochem. J. 24:1987;743-748.
31. Piomelli D. Arachidonic acid in cell signaling. Curr. Opin. Cell Biol. 5:1993;274-280.
32. Di Marzo V. Arachidonic acid and eicosanoids as targets and effectors in second messenger interactions. Prostaglandins Leukotrienes Essent. Fatty Acids. 53:1995;239-254.
33. Entwistle A., Curtis D. H., Zalin R. J. Myoblast fusion is regulated by a prostanoid of the one serie independently of a rise in cyclic AMP. J. Cell Biol. 103:1986;857-866.
34. Zalin R. J. The role of hormones and prostaglandins in thein vitro. Exp. Cell Res. 172:1987;265-281.
35. Elgendy H., Hausman R. E. Prostaglandin-dependant phosphatidylinositol signaling during embryonic chick myogenesis. Cell Differ. Dev. 32:1990;109-115.
36. McLennan I. S. E and F alpha series prostaglandins in developing muscles. Prostaglandins Leukotrienes Essent. Fatty Acids. 43:1991;77-82.
37. Keller H., Dreyer C., Medin J., Mahfoudi A., Ozato K., Wahli W. Fatty acids and retinoids control lipid metabolism through activation of peroxisome proliferator-activated receptor-retinoid X receptor heterodimers. Proc. Natl. Acad. Sci. USA. 90:1993;2160-2164.
38. Park K. S., Ciaraldi T. P., Abramscarter L., Mudaliar S., Nikoulina S. E., Henry R. R. PPAR gamma gene expression is elevated in skeletal muscle of OBESE and type II diabetic subjects. Diabetes. 46:1997;1230-1234.
39. Elbrecht A., Chen Y. L., Cullinan C. A., Hayes N., Leibowitz M. D., Moller D. E., Berger J. Molecular cloning expression and characterization of human peroxisome proliferation activated receptors gamma 1 and gamma 2. Biochem. Biophys. Res. Commun. 224:1996;431-437.