Expression and physiological regulation of BDNF receptors in the neuroendocrine melanotrope cell of Xenopus laevis

General and Comparative Endocrinology

Volumn 153, Issue 1-3, 2007, Pages 176-181

  Kidane, Adhanet H ^a   van Dooren, Sander H J ^a   Roubos, Eric W ^a   Jenks, Bruce G ^a  

^a EURON European Graduate School of Neuroscience   (Netherlands)

Author keywords

BDNF; Melanotrope; p75NTR; Pars intermedia; TrkB; MSH

Indexed keywords

ALPHA INTERMEDIN; BRAIN DERIVED NEUROTROPHIC FACTOR; BRAIN DERIVED NEUROTROPHIC FACTOR RECEPTOR; NEUROTROPHIN RECEPTOR;

ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; CONTROLLED STUDY; HYPOPHYSIS INTERMEDIATE LOBE; IN SITU HYBRIDIZATION; NEUROSECRETORY CELL; NONHUMAN; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN EXPRESSION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; XENOPUS LAEVIS;

EID: 34547104839     PISSN: 00166480     EISSN: 10956840     Source Type: Journal    
DOI: 10.1016/j.ygcen.2007.04.001     Document Type: Article

References (27)

1. Biffo S., Offenhauser N., Carter B.D., and Barde Y.A. Selective binding and internalisation by truncated receptors restrict the availability of BDNF during development. Development 121 (1995) 2461-2470
2. Chao M. Neurotrophins and their receptors: a convergence point for many signalling pathways. Nature Rev. Neurosci. 4 (2003) 299-309
3. De Rijk E.P.C.T., Jenks B.G., and Wendelaar Bonga S.E. Morphology of the pars intermedia and the melanophore-stimulating cells in Xenopus laevis in relation to background adaptation. Gen. Comp. Endocrinol. 79 (1990) 74-82
4. Eide F.F., Vining E.R., Eide B.L., Zang K., Wang X.-Y., and Reichardt L.F. Naturally occurring truncated TrkB receptors have dominant inhibitory effects on Brain-Derived Neurotrophic Factor signaling. J. Neurosci. 16 (1996) 3123-3129
5. Esposito D., Patel P., Stephens R.M., Perez P., Chao M.V., Kaplan D.R., and Hempstead B.L. The cytoplasmic and transmembrane domains of the p75 and Trk A receptors regulate high affinity binding to nerve growth factor. J. Biol. Chem. 276 (2001) 32687-32695
6. Hartmann M., Brigadski T., Erdmann K.S., Holtmann B., Sendtner M., Narz F., and Lessmann V. Truncated TrkB receptor-induced outgrowth of dendritic filopodia involves the p75 neurotrophin receptor. J. Cell Sci. 117 (2004) 5803-5814
7. Huang E.J., and Reichardt L.F. Trk receptors: roles in neuronal transduction. Annu. Rev. Biochem. 72 (2003) 609-642
8. 2+ oscillations in melanotropes of Xenopus laevis: their generation, propagation, and function. Gen. Comp. Endocrinol. 131 (2003) 209-219
9. Jing S., Tapley P., and Barbacid M. Nerve growth factor mediates signal transduction through trk homodimer receptors. Neuron 9 (1992) 1067-1069
10. Kingsbury T.J., Murray P.D., Bambrick L.L., and Krueger B.K. Ca(2+)-dependent regulation of TrkB expression in neurons. J. Biol. Chem. 17 (2003) 407-448
11. Klein R., Conway D., Parada L.F., and Barbacid M. The TrkB tyrosine protein kinase gene codes for a second neurogenic receptor that lacks the catalytic kinase domain. Cell 65 (1990) 189-197
12. Kramer B.M.R., Cruijsen P.M.J.M., Ouwens D.T.W.M., Coolen M.W., Martens G.J.M., Roubos E.W., and Jenks B.G. Evidence that brain-derived neurotrophic factor acts as an autocrine factor on pituitary melanotrope cells of Xenopus laevis. Endocrinology 143 (2002) 1337-1345
13. Lee R., Kermani P., Teng K.K., and Hempstead B.L. Regulation of cell survival by secreted proneurotrophins. Science 294 (2001) 1945-1948
14. Luikart B.W., Nef S., Shipman T., and Parada L.F. In vivo role of truncated trkb receptors during sensory ganglion neurogenesis. Neuroscience 117 (2003) 847-858
15. Martens G.J.M., Weterings K.A.P., van Zoest I.D., and Jenks B.G. Physiologically-induced changes in proopiomelanocortin mRNA levels in the pituitary gland of the amphibian Xenopus laevis. Biochem. Biophys. Res. Comm. 143 (1987) 678-684
16. Middlemas D.S., Lindberg R.A., and Hunter T. TrkB, a neural receptor protein-tyrosine kinase: evidence for a full-length and two truncated receptors. Mol. Cell. Biol. 11 (1991) 143-153
17. Ninkinal N., Grashchuck M., Buchman V.L., and Davies A.M. TrkB variants with deletions in the leucine-rich motifs of the extracellular domain. J. Biol. Chem. 272 (1997) 13019-13025
18. Nykjaer A., Lee R., Teng K.K., Jansen P., Madesen P., Nielsen M.S., Jacobsen C., Kliemannel M., Schwartz E., Willnow T.E., Hempstead B.L., and Petersen C.M. Sortilin is essential for proNGF-induced neuronal cell death. Nature 427 (2004) 843-848
19. NTR-live or let die. Curr. Opin. Neurobiol. 15 (2005) 49-57
20. Ohira K., Homma K.J., Hirai H., Nakamura S., and Hayashi M. TrkB-T1 regulates the RhoA signaling and actin cytoskeleton in glioma cells. Biochem. Biophys. Res. Commun. 342 (2006) 867-874
21. Ohira K., Kumanogoh H., Sahara Y., Homma K.J., Hirai H., Nakamura S., and Hayashi M. A truncated tropo-myosine-related kinase B receptor, T1, regulates glial cell morphology via Rho GDP dissociation inhibitor 1. J. Neurosci. 25 (2005) 1343-1353
22. Rose C.R., Blum R., Pichler B., Lepier A., Kafitz K.W., and Konnerth A. Truncated TrkB-T1 mediates neurotrophin-evoked calcium signaling in glia cells. Nature 426 (2003) 74-78
23. Roubos E.W., Scheenen W.J.J.M., and Jenks B.G. Neuronal, nonneuronal, and autocrine control of Xenopus melanotrope cell activity. Ann. NY Acad. Sci. 1040 (2005) 172-183
24. Shelton D.L., Sutherland J., Gripp J., Camerato T., Armanini M.P., Philips H.S., Carroll K., Spencer S.D., and Levinson A.D. Human trks: molecular cloning, tissue distribution, and expression of extracellular domain immunoadhesins. J. Neurosci. 15 (1995) 477-491
25. Ullrich A., and Schlessinger J. Signal transduction by receptors with tyrosine kinase activity. Cell 61 (1990) 203-212
26. Wang L.C., Meijer H.K., Humbel B.M., Jenks B.G., and Roubos E.W. Activity-dependent dynamics of coexisting brain derived neurotrophic factor, pro-opiomelanocortin and α-melanophore-stimulating hormone in melanotrope cells of Xenopus laevis. J. Neuroendocrinol. 16 (2004) 19-25
27. Weatherhead B., Thornton V.F., and Whur P. Effects of change of background colour on the ultrastructure of the'MSH cells' of the pars intermedia of Xenopus laevis. J. Endocrinol. 49 (1971) 25-26