The effect of tetrahydrobiopterin on the in situ phosphorylation of tyrosine hydroxylase in rat striatal synaptosomes
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Abstract
Tetrahydrobiopterin (BH4), the obligatory cofactor of the aromatic amino acid hydroxylases, decreased the in situ32P-phosphorylation of tyrosine hydroxylase (TH) in rat striatal synaptosomes. Incubation of pre-32P-labeled synaptosomes with BH4 in the presence of a permeant analogue of cAMP decreased the cAMP-stimulated level of32P label incorporation into TH by about 50%, as determined by immunoprecipitation and autoradiography of SDS-polyacrylamide gels. The extent of inhibition mirrored changes in intrasynaptosomal BH4 levels and varied both as a function of BH4 concentration and length of incubation. A similar decrease in the amount of TH32P-labeling was observed with the precursor of BH4, sepiapterin. This effect, in turn, was reversed by the inhibitor of sepiapterin reductase, N-acetyl-serotonin. Finally, exposure of pre-32P-labeled synaptosomes to the inhibitor of protein phosphatase 2A, okadaic acid, blocked the response to BH4. Collectively, the data suggest that BH4 stimulates the dephosphorylation of TH in situ and thus may play a dual role both as a cofactor for catalysis and a regulator of hydroxylase activity.
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Tetrahydrobiopterin tyrosine hydroxylase phosphorylation synaptosomesPreview
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References
- 1.Kaufman, S. 1987. Aromatic amino acid hydroxylases pages 217–282,in The Enzymes, Vol. 18, Academic Press, Orlando. Fl.Google Scholar
- 2.Fukushima, T., and Nixon, J. C. 1980. Analysis of reduced forms of biopterin in biological tissues and fluids. Anal. Biochem. 102:176–188.Google Scholar
- 3.Milstien, S. 1987. Tetrahydrobiopterin: Other physiological roles in addition to aromatic amino acid hydroxylation. Pages 49–65,in Curtius, H. Ch., Blau, N., and Levine, R. A. (eds.) Unconjugated Pterins and Related Biogenic Amines, de Gruyter, Berlin.Google Scholar
- 4.Tanaka, K., Kaufman, S., and Milstien, S. 1989. Tetrahydrobiopterin, the cofactor for aromatic amino acid hydroxylases, is synthesized by and regulates proliferation of crythroid cells. Proc. Natl. Acad. Sci. USA 86:5864–5867.Google Scholar
- 5.Koshimura, K., Miwa, S., Lee, K., Fugiwara, M., and Watanabe, Y. 1990. Enhancement of dopamine release in vivo from the rat striatum by dialytic perfusion of 6R-L-erythro-5,6,7,8-tetrahydrobiopterin. J. Neurochem. 54:1391–1397.Google Scholar
- 6.Mataga, N., Imamura, K., and Watanabe, Y. 1991. 6R-Tetrahydrobiopterin perfusion enhances dopamine, serotonin, and glutamate outputs in dialysate from rat striatum and frontal cortex. Brain Res. 551:64–71.Google Scholar
- 7.Tayeh, M. A., and Marletta, M. A. 1989. Macrophage oxidation of arginine to nitric oxide, nitrite and nitrate J. Biol. Chem. 264:19654–196458.Google Scholar
- 8.Kwon, N. S., Nathan, C. F., and Stuehr, D. J. 1989. Reduced biopterin as a cofactor in the generation of nitrogen oxides by murine macrophages. J. Biol. Chem. 264:20496–20501.Google Scholar
- 9.Mayer, B., John, M., Heinzel, B., Werner, E. R., Wachter, H., Schultz, G., and Bohme, E. 1991. Brain nitric oxide is a biopterin-and flavin-containing multi-functional oxido-reductase. FEBS Lett. 288:187–191.Google Scholar
- 10.Giovanelli, J., Campos, K. L., and Kaufman, S. 1991. Tetrahydrobiopterin, a cofactor for rat cerebellar nitric oxide synthase, does not function as a reactant in the oxygenation of arginine. Proc. Natl. Acad. Sci. USA 88:7091–7095.Google Scholar
- 11.Nelson, T. J., and Kaufman, S. 1987. Activation of rat caudate tyrosine hydroxylase phosphatase by tetrahydropterins J. Biol. Chem. 262:16470–16475.Google Scholar
- 12.Campbell, D. G., Hardie, D. G., and Viullet, P. R. 1986. Identification of four phosphorylation sites in the N-terminal region of tyrosine hydroxylase. J. Biol. Chem 261:10489–10492.Google Scholar
- 13.Funakoshi, H., Okuno, S., and Fujisawa, H. 1991. Different effects on activity caused by phosphorylation of tyrosine hydroxylase at serine 40 by three multifunctional protein kinases. J. Biol. Chem. 266:15614–15620.Google Scholar
- 14.Haycock, J. W., and Haycock, D. A. 1991. Tyrosine hydroxylase in rat brain dopaminergic nerve terminals. J. Biol. Chem. 266:5650–5657.Google Scholar
- 15.Zigmond, R. E., Schwarzschild, M. A., and Rittenhouse A. R. 1989. Acute regulation of tyrosine hydroxylase by nerve activity and by neurotransmitters via phosphorylation. Ann. Rev. Neurosci. 12:415–461.Google Scholar
- 16.Boarder, M. R., and Fillenz, M. 1979. Synaptosomal tyrosine hydroxylation in the rat brain: comparison of activity from hippocampus and hypothalamus with activity from striatum. J. Neurochem. 31:1419–1425.Google Scholar
- 17.Colby, K. A., Thompson, T. L., and Patrick, R. L. 1989. Tyrosine hydroxylase phosphorylation in rat brain striatal synaptosomes. Brain Res. 478:103–111.Google Scholar
- 18.Laemmli, U. K. 1970. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature (Lond.) 227:680–685.Google Scholar
- 19.O'Neil, R. R., Mitchell, L. G., Merril, C. R., and Rasband, W. S. 1989. Use of image analysis to quantitate changes in form of mitochondrial DNA after x-irradiation. Appl. and Theor. Electrophor. 1:163–167.Google Scholar
- 20.Milstien, S., and Kaufman, S. 1989. The biosynthesis of tetrahydrobiopterin in rat brain. J. Biol. Chem. 264:8066–8073.Google Scholar
- 21.Nagatsu, T., Levitt, M., and Udenfriend, S. 1964. A rapid and simple radioassay for tyrosine hydroxylase activity. Anal. Biochem. 9:122–126.Google Scholar
- 22.Richtand, N. M., Inagami, T., Misono, K., and Kuczenski, R. 1985. Purification and characterization of rat striatal tyrosine hydroxylase. J. Biol. Chem. 260:8465–8473.Google Scholar
- 23.Hawkins, P. T., Michell, R. H., and Kirk, C. J. 1983. A simple assay method for determination of the specific radioactivity of the γ-phosphate group of32P-labelled ATP. Biochem. J. 210:717–720.Google Scholar
- 24.Katoh, S., Sucoka, T., and Yamada, S. 1982. Direct inhibition of brain sepiapterin reductase by a catecholamine and an indoleamine. Biochem. Biophys. Res. Commun. 105:75–81.Google Scholar
- 25.Anastasiadis, P. Z., Wolf, W. A., Levine, R. A., and Kuhn, D. M. 1989. Studies of tetrahydrobiopterin uptake in rat brain synaptosomes. Pages 648–651,in Curtius, H-Ch., Ghisla, S. and Blau, N. (eds.) Chemistry and Biology of Pteridines: Pteridines and Folic Acid Derivatives. Walter de Gruyter, Berlin.Google Scholar
- 26.Dhondt, J. L., Hoyte, J. M., Noel, C., and Farriaux, J. P. 1989. Membrane transport of unconjugated pterins, the model of human erythrocytes. Pages 543–546in Curtius, H.-Ch., Ghisla, S. and Blau, N. (eds.) Chemistry and Biology of Pteridines: Pteridines and Folic Acid Derivatives. Walter de Gruyter, Berlin.Google Scholar
- 27.Cohen, P., and Cohen, P. T. W. 1989. Protein phosphatases come of age. J. Biol. Chem. 264:21435–21438.Google Scholar
- 28.Haavik, J., Schelling, D. L., Campbell, D. G., Andersson, K. K., Flatmark, T., and Cohen, P. 1989. Identification of protein phosphatase 2A as the major tyrosine hydroxylase phosphatase in adrenal medulla and corpus striatum: evidence from the effects of okadaic acid. FEBS lett. 251:36–42.Google Scholar
- 29.Levine, R. A., Kapatos, G., Kaufman, S., and Milstien, S. 1990. Immunological evidence for the requirement of sepiapterin reductase for tetrahydrobiopterin biosynthesis in brain. J. Neurochem. 54:1218–1224.Google Scholar
- 30.Kaufman, S., Hasegawa, H., Wilgus, H., and Parniak, M. 1981. Regulation of hepatic phenylalanine hydroxylase by phosphorylation and dephosphorylation. Pages 1391–1405,in Cold Spring Harbor Conferences on Cell Proliferation, Vol. 8.Google Scholar
- 31.Salah, R. S., Kuhn, D. M., and Galloway, M. P. 1989. Dopamine autoreceptors modulate the phosphorylation of tyrosine hydroxylase in rat striatal slices. J. Neurochem. 52:1517–1522.Google Scholar