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Transcriptional Regulation of the Tyrosine Hydroxylase Gene by Neurotensin in Human Neuroblastoma CHP212 Cells

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Abstract

The human neuroblastoma cell line CHP212 was found to express functional high affinity neurotensin (NTS-1) receptor subtype. Based on the functional interactions between neurotensin and dopamine transmission, we have used this cell line to investigate the short- and long-term modulation of tyrosine hydroxylase gene expression by the stable neurotensin agonist JMV 449. After exposure of the cells to 1 μM JMV 449 for 5 or 72 h, tyrosine hydroxylase protein and mRNA levels were significantly increased as detected by western blot analysis and quantitative RT-PCR, respectively. Transfection of CHP212 cells with a plasmid containing the luciferase reporter gene under the control of a limited proximal region of the cloned tyrosine hydroxylase promoter, revealed that the effect of JMV 449 results from an increase in the transcriptional activity of the TH gene. These results indicate that modulation of tyrosine hydroxylase gene expression may constitute one of the mechanisms involved in the control of dopamine transmission by neurotensin. Such neurotensin-mediated changes in tyrosine hydroxylase expression may also participate in multiple adaptation processes within the central nervous system to environmental conditions where neurotensin is released such as stress and food intake.

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REFERENCES

  • Arbogast, L.A. and Voogt, J.L. (1991). Mechanisms of tyrosine hydroxylase regulation during pregnancy: Evidence for protein dephosphorylation during the prolactin surges. Endocrinology 129:2575–2582.

    Google Scholar 

  • Azzi, M., Betancur, C., Sillaber, I., Spangel, R., Rostene,W., and Berod, A. (1998). Repeated administration of the neurotensin receptor antagonist SR 48692 differentially regulates mesocortical and mesolimbic dopaminergic systems. J. Neurochem. 71:1158–1167.

    Google Scholar 

  • Berry, S.A. and Gudelsky, G.A. (1992). Evidence for protein kinase-C mediation of the neurotensin-induced activation of tyrosine hydroxylase in tuberoinfundibular dopaminergic neurons. Endocrinology 131:1207–1211.

    Google Scholar 

  • Betancur, C., Cabrera, R., De Kloet, E.R., Pelaprat, D., and Rostène, W. (1998). Role of endogenous neurotensin in the behavioral and neuroendocrine effects of cocaine. Neuropsychopharmacology 19:322–332.

    Google Scholar 

  • Bradford, M.M. (1976). A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72:248–254.

    Google Scholar 

  • Burgevin, M.C., Castel, M.N., Quarteronet, D., Chevet, T., and Laduron, P.M. (1992). Neurotensin increases tyrosine hydroxylase messenger RNA-positive neurons in substantia nigra after retrograde axonal transport. Neuroscience 49:627–633.

    Google Scholar 

  • Cambi, F., Fung, B., and Chikaraishi, D. (1989). 50 flanking DNA sequences direct cell-specific expression of rat tyrosine hydroxylase. J. Neurochem. 53:1656–1659.

    Google Scholar 

  • Chae, H.D., Suh, B.C., Joh, T.H., and Kim, K.T. (1996). AP1-mediated transcriptional enhancement of the rat tyrosine hydroxylase gene by muscarinic stimulation. J. Neurochem. 66:1264–1272.

    Google Scholar 

  • Chirgwin, J.M., Przybyla, A.E., MacDonald, R.J., and Rutter, W.J. (1979). Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease. Biochemistry 18:5294–5299.

    Google Scholar 

  • Cho, S., Neff, N.H., and Hadjiconstantinou, M. (1997). Regulation of tyrosine hydroxylase and aromatic L-amino acid decarboxylase by dopaminergic drugs. Eur. J. Pharmacol. 323:149–157.

    Google Scholar 

  • Coker, G.T., Vinnedge, L., and O'Malley, K.L. (1988). Characterization of rat and human tyrosine hydroxylase genes: Functional expression of both promoters in neuronal and non-neuronal cell types. Biochem. Biophys. Res. Commun. 157:1341–1347.

    Google Scholar 

  • De Quidt, M.E. and Emson, P.C. (1983). Neurotensin facilitates dopamine release in vitro from rat striatal slices. Brain Res. 274:376–380.

    Google Scholar 

  • Doulut, S., Rodriguez, M., Lugrin, D., Vecchini, F., Kitabgi, P., Aumelas, A., and Martinez, J. (1992). Reduced peptide bond pseudopeptide analogues of neurotensin. Pept. Res. 5:30–38.

    Google Scholar 

  • Haavik, J. and Toska, K. (1998). Tyrosine hydroxylase and Parkinson's disease. Mol. Neurobiol. 16:285–309.

    Google Scholar 

  • Hermans, E., Gailly, P., Octave, J.N., and Maloteaux, J.M. (1994). Rapid desensitization of agonist-induced calcium mobilization in transfected PC12 cells expressing the rat neurotensin receptor. Biochem. Biophys. Res. Commun. 198:400–407.

    Google Scholar 

  • Kasckow, J. and Nemeroff, C.B. (1991). The neurobiology of neurotensin: Focus on neurotensin-dopamine interactions. Regul. Pept. 36:153–164.

    Google Scholar 

  • Kilbourne, E.J., Nankova, B.B., Lewis, E.J., McMahon, A., Osaka, H., Sabban, D.B., and Sabban, E.L. (1992). Regulated expression of the tyrosine hydroxylase gene by membrane depolarization. Identification of the responsive element and possible second messengers. J. Biol. Chem. 267:7563–7569.

    Google Scholar 

  • Kitabgi, P., Checler, F., Mazella, J., and Vincent, J.P. (1985). Pharmacology and biochemistry of neurotensin receptors. Rev. Clin. Basic Pharm. 5:397–486.

    Google Scholar 

  • Kitabgi, P. and Nemeroff, C.B. (1992). The neurobiology of neurotensin. Proceeding of the 2nd international conference on neurotensin. Ann. NY Acad. Sci. 668:1–371.

    Google Scholar 

  • Laduron, P.M. (1995). Functional consequences of retrograde axonal transport of receptor-bound neurotensin. Trends Pharmacol. Sci. 16:338–343.

    Google Scholar 

  • Laemmli, U.K. (1970). Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227:680–685.

    Google Scholar 

  • Lambert, P.D., Gross, R., Nemeroff, C.B., and Kilts, C.D. (1995). Anatomy and mechanisms of neurotensindopamine interactions in the central nervous system. Ann. NY Acad. Sci. 757:377–389.

    Google Scholar 

  • Mallet, J. (1996). Catecholamines: From gene regulation to neuropsychiatric disorders. Trends Neurosci. 19:191–196.

    Google Scholar 

  • Muller, A., Monnier, D., Rene, F., Larmet, Y., Koch, B., and Loeffler, J.P. (1997). Pituitary adenylate cyclaseactivating polypeptide triggers dual transduction signaling in CATHa cells and transcriptionally activates tyrosine hydroxylase and c-fos expression. J. Neurochem. 68:1696–1704.

    Google Scholar 

  • Najimi, M., Souaze, F., Mendez, M., Hermans, E., Berbar, T., Rostene, W., and Forgez, P. (1998). Activation of receptor gene transcription is required to maintain cell sensitization after agonist exposure. Study on neurotensin receptor. J. Biol. Chem. 273:21634–21641.

    Google Scholar 

  • Nemeroff, C.B., Luttinger, D., Hernandez, D.E., Mailman, R.B., Mason, G.A., Davis, S.D., Widerlov, E., Frye, G.D., Kilts, C.A., Beaumont, K., Breese, G.R., and Prange, A.J. (1983). Interactions of neurotensin with brain dopamine systems: Biochemical and behavioral studies. J. Pharmacol. Exp. Ther. 225:337–345.

    Google Scholar 

  • Sambrook, J., Fritsch, E.F., and Maniatis, T. (1989). Molecular Cloning: A Laboratory Manual, 2nd edn., Cold Spring Harbor Laboratory Press, New York.

    Google Scholar 

  • Sato, M., Shiosaka, S., and Tohyama, M. (1991). Neurotensin and neuromedin N elevate the cytosolic calcium concentration via transiently appearing neurotensin binding sites in cultured rat cortex cells. Brain Res. Dev. Brain Res. 58:97–103.

    Google Scholar 

  • Souazé, F., Ntodou-Thome, A., Tran, C.Y., Rostene, W., and Forgez, P. (1996). Quantitative RT-PCR: Limits and accuracy. Biotechniques 21:280–285.

    Google Scholar 

  • Stachowiak, M.K., Jiang, H.K., Poisner, A.M., Tuominen, R.K., and Hong, J.S. (1990). Short and long-term regulation of catecholamine biosynthetic enzymes by angiotensin in cultured adrenal medullary cells. Molecular mechanisms and nature of second messenger systems. J. Biol. Chem. 265:4694–4702.

    Google Scholar 

  • Towbin, H., Staehelin, T., and Gordon, J. (1979). Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: Procedure and some applications. Proc. Natl. Acad. Sci. USA 76:4350–4354.

    Google Scholar 

  • Vincent, J.P., Mazella, J., and Kitabgi, P. (1999). Neurotensin and neurotensin receptors. Trends Pharmacol. Sci. 20:302–309.

    Google Scholar 

  • Vita, N., Laurent, P., Lefort, S., Chalon, P., Dumont, X., Kaghad, M., Gully, D., Le Fur, G., Ferrara, P., and Caput, D. (1993). Cloning and expression of a complementary DNA encoding a high affinity human neurotensin receptor. FEBS Lett. 317:139–142.

    Google Scholar 

  • Wessels-Reiker, M., Basiboina, R., Howlett, A.C., and Strong, R. (1993). Vasoactive intestinal polypeptide-related peptides modulate tyrosine hydroxylase gene expression in PC12 cells through multiple adenylate cyclasecoupled receptors. J. Neurochem. 60:1018–1029.

    Google Scholar 

  • Widerlov, E., Kilts, C.D., Mailman, R.B., Nemeroff, C.B., Mc Cown, T.J., Prange, A.J., and Breese, G.R. (1982). Increase in dopamine metabolites in rat brain by neurotensin. J. Pharmacol. Exp. Ther. 223:1–6.

    Google Scholar 

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Correspondence to Mustapha Najimi.

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Najimi, M., Hermans, E., Rostène, W. et al. Transcriptional Regulation of the Tyrosine Hydroxylase Gene by Neurotensin in Human Neuroblastoma CHP212 Cells. Metab Brain Dis 16, 165–174 (2001). https://doi.org/10.1023/A:1012588927052

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