Vasopressin-induced translocation and proteolysis of protein kinase Cα in an amphibian brain: Modulation by corticosterone

Brain Research

Volumn 1134, Issue 1, 2007, Pages 18-26

  Gasser, Paul J ^a   Orchinik, Miles ^a  

^a ARIZONA STATE UNIVERSITY   (United States)

Author keywords

Corticosterone; PKC; Proteolysis; Translocation; Vasopressin; Vasotocin

Indexed keywords

ARGIPRESSIN; ARGIPRESTOCIN; CORTICOSTERONE; ENZYME; PROTEIN KINASE C ALPHA; PROTEIN KINASE M ALPHA; UNCLASSIFIED DRUG; VASOPRESSIN;

AMPHIBIA; ANALYTIC METHOD; ANIMAL TISSUE; ARTICLE; BRAIN TISSUE; CONTROLLED STUDY; CYTOSOLIC FRACTION; FEMALE; IMMUNOREACTIVITY; MALE; NONHUMAN; PRIORITY JOURNAL; PROTEIN DEGRADATION; PROTEIN TRANSPORT; SALAMANDER; SIGNAL TRANSDUCTION; WESTERN BLOTTING;

AMBYSTOMA; ANIMALS; ARGININE VASOPRESSIN; BRAIN; CATALYTIC DOMAIN; CELL MEMBRANE; CORTICOSTERONE; CYTOSOL; FEMALE; MALE; PEPTIDE HYDROLASES; PROTEIN KINASE C; PROTEIN KINASE C-ALPHA; PROTEIN TRANSPORT; RECEPTORS, VASOPRESSIN;

AMBYSTOMA TIGRINUM; AMPHIBIA; VERTEBRATA;

EID: 33846380714     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.brainres.2006.11.071     Document Type: Article

References (57)

1. Acharjee S., Do-Rego J.L., Oh D.Y., Moon J.S., Ahn R.S., Lee K., Bai D.G., Vaudry H., Kwon H.B., and Seong J.Y. Molecular cloning, pharmacological characterization, and histochemical distribution of frog vasotocin and mesotocin receptors. J. Mol. Endocrinol. 33 (2004) 293-313
2. Akhundova A., Getmanova E., Gorbulev V., Carnazzi E., Eggena P., and Fahrenholz F. Cloning and functional characterization of the amphibian mesotocin receptor, a member of the oxytocin/vasopressin receptor superfamily. Eur. J. Biochem. 237 (1996) 759-767
3. Ali N., Kantachuvesiri S., Smallwood J.I., Macala L.J., Isales C., Ji J., Reilly R., and Hayslett J.P. Vasopressin-induced activation of protein kinase C in renal epithelial cells. Biochim. Biophys. Acta 1402 (1998) 188-196
4. Ancellin N., and Morel A. Homologous and heterologous acute desensitization of vasopressin V1a receptor in Xenopus oocytes. Cell Signalling 10 (1998) 217-223
5. Boldyreff B., and Wehling M. Aldosterone: refreshing a slow hormone by swift action. News Physiol. Sci. 19 (2004) 97-100
6. Bolsover S.R., Gomez-Fernandez J.C., and Corbalan-Garcia S. Role of the Ca2+/phosphatidylserine-binding region of the C2 domain in the translocation of Protein Kinase Calpha to the plasma membrane. J. Biol. Chem. (2003) 10282-10290
7. Boyd S.K., and Moore F.L. Autoradiographic localization of putative arginine vasotocin receptors in the kidney of a urodele amphibian. Gen. Comp. Endocrinol. 78 (1990) 344-350
8. Boyd S.K., and Moore F.L. Gonadectomy reduces the concentrations of putative receptors for arginine vasotocin in the brain of an amphibian. Brain Res. 541 (1991) 193-197
9. Bradford M.M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72 (1976) 248-254
10. Chiyo T., Yamazaki T., Aoshika K., Kominami S., and Ohta Y. Corticosterone enhances adrenocorticotropin-induced calcium signals in bovine adrenocortical cells. Endocrinology 144 (2003) 3376-3381
11. Coddington E., and Moore F.L. Neuroendocrinology of context-dependent stress responses: vasotocin alters the effect of corticosterone on amphibian behaviors. Horm. Behav. 43 (2003) 222-228
12. Cohen J., Cohen P., West S.G., and Aiken L.S. Applied Multiple regression/correlation analysis for the behavioral sciences. In: Reigert D. (Ed) (2003), Lawrence Erlbaum Associates, Inc, Mahwah, NY 1-703
13. Cressman C.M., Mohan P.S., Nixon R.A., and Shea T.B. Proteolysis of protein kinase C: mM and microM calcium-requiring calpains have different abilities to generate, and degrade the free catalytic subunit, protein kinase M. FEBS Lett. 367 (1995) 223-227
14. ffrench-Mullen J.M. Cortisol inhibition of calcium currents in guinea pig hippocampal CA1 neurons via G-protein-coupled activation of protein kinase C. J. Neurosci. 15 (1995) 903-911
15. Gasser P.J., Lowry C.A., and Orchinik M. Corticosterone-sensitive monoamine transport in the rat dorsomedial hypothalamus: potential role for organic cation transporter 3 in stress-induced modulation of monoaminergic neurotransmission. J. Neurosci. 26 (2006) 8758-8766
16. Goodson J.L., and Bass A.H. Social behavior functions and related anatomical characteristics of vasotocin/vasopressin systems in vertebrates. Brain Res. Brain Res. Rev. 35 (2001) 246-265
17. Han J.Z., Lin W., Lou S.J., Qiu J., and Chen Y.Z. A rapid, nongenomic action of glucocorticoids in rat B103 neuroblastoma cells. Biochim. Biophys. Acta 1591 (2002) 21-27
18. He L.M., Zhang C.G., Zhou Z., and Xu T. Rapid inhibitory effects of corticosterone on calcium influx in rat dorsal root ganglion neurons. Neuroscience 116 (2003) 325-333
19. Innamorati G., Sadeghi H., and Birnbaumer M. Transient phosphorylation of the V1a vasopressin receptor. J. Biol. Chem. 273 (1998) 7155-7161
20. Kasai M., and Yamashita H. Inhibition by cortisol of neurons in the paraventricular nucleus of the hypothalamus in adrenalectomized rats; an in vitro study. Neurosci. Lett. 91 (1988) 59-64
21. Kohno S., Kamishima Y., and Iguchi T. Molecular cloning of an anuran V(2) type [Arg(8)] vasotocin receptor and mesotocin receptor: functional characterization and tissue expression in the Japanese tree frog (Hyla japonica). Gen. Comp. Endocrinol. 132 (2003) 485-498
22. Larcher A., Delarue C., Homo-Delarche F., Kikuyama S., Kupryszewski G., and Vaudry H. Pharmacological characterization of vasotocin stimulation of phosphoinositide turnover in frog adrenal gland. Endocrinology 130 (1992) 475-483
23. Lewis C.M., Dolence E.K., Hubbard C.S., and Rose J.D. Identification of roughskin newt medullary vasotocin target neurons with a fluorescent vasotocin conjugate. J. Comp. Neurol. 491 (2005) 381-389
24. Lewis C.M., Dolence E.K., Zhang Z., and Rose J.D. Fluorescent vasotocin conjugate for identification of the target cells for brain actions of vasotocin. Bioconjugate Chem. 15 (2004) 909-914
25. Li C., Fultz M.E., and Wright G.L. PKC-alpha shows variable patterns of translocation in response to different stimulatory agents. Acta Physiol. Scand. 174 (2002) 237-246
26. Ling D.S., Benardo L.S., and Sacktor T.C. Protein kinase Mzeta enhances excitatory synaptic transmission by increasing the number of active postsynaptic AMPA receptors. Hippocampus (2006) 443-452
27. Liu J.P., Engler D., Funder J.W., and Robinson P.J. Evidence that the stimulation by arginine vasopressin of the release of adrenocorticotropin from the ovine anterior pituitary involves the activation of protein kinase C. Mol. Cell. Endocrinol. 87 (1992) 35-47
28. Mahlmann S., Meyerhof W., Hausmann H., Heierhorst J., Schonrock C., Zwiers H., Lederis K., and Richter D. Structure, function, and phylogeny of [Arg8]vasotocin receptors from teleost fish and toad. Proc. Natl. Acad. Sci. U. S. A. 91 (1994) 1342-1345
29. Moore F.L., and Miller L.J. Arginine vasotocin induces sexual behavior of newts by acting on cells in the brain. Peptides 4 (1983) 97-102
30. Muslimov I.A., Nimmrich V., Hernandez A.I., Tcherepanov A., Sacktor T.C., and Tiedge H. Dendritic transport and localization of protein kinase Mzeta mRNA: implications for molecular memory consolidation. J. Biol. Chem. 279 (2004) 52613-52622
31. Newton A.C. Regulation of the ABC kinases by phosphorylation: protein kinase C as a paradigm. Biochem. J. 370 (2003) 361-371
32. Orchinik M., Gasser P.J., and Breuner C.W. Rapid corticosteroid actions on behavior: cellular mechanisms and organismal consequences. In: Pfaff D.W. (Ed). Hormones, Brain and Behavior (2002), Academic Press
33. Orchinik M., Matthews L., and Gasser P.J. Distinct specificity for corticosteroid binding sites in amphibian cytosol, neuronal membranes, and plasma. Gen. Comp. Endocrinol. 118 (2000) 284-301
34. Orchinik M., Murray T.F., and Moore F.L. A corticosteroid receptor in neuronal membranes. Science 252 (1991) 1848-1851
35. Ouyang M., and Wang S. Dexamethasone attenuates the depressor response induced by neuropeptide Y microinjected into the nucleus tractus solitarius in rats. Br. J. Pharmacol. 129 (2000) 865-870
36. Pontremoli S., Michetti M., Melloni E., Sparatore B., Salamino F., and Horecker B.L. Identification of the proteolytically activated form of protein kinase C in stimulated human neutrophils. Proc. Natl. Acad. Sci. 87 (1990) 3705-3707
37. Qiu J., Wang C.G., Huang X.Y., and Chen Y.Z. Nongenomic mechanism of glucocorticoid inhibition of bradykinin-induced calcium influx in PC12 cells: possible involvement of protein kinase C. Life Sci. 72 (2003) 2533-2542
38. Rose J.D., Kinnaird J.R., and Moore F.L. Neurophysiological effects of vasotocin and corticosterone on medullary neurons: implications for hormonal control of amphibian courtship behavior. Neuroendocrinology 62 (1995) 406-417
39. Rose J.D., and Moore F.L. A neurobehavioral model for rapid actions of corticosterone on sensorimotor integration. Steroids 64 (1999) 92-99
40. Rose J.D., and Moore F.L. Behavioral neuroendocrinology of vasotocin and vasopressin and the sensorimotor processing hypothesis. Front. Neuroendocrinol. 23 (2002) 317-341
41. Sabatier N., Richard P., and Dayanithi G. L-, N- and T-but neither P-nor Q-type Ca2+ channels control vasopressin-induced Ca2+ influx in magnocellular vasopressin neurones isolated from the rat supraoptic nucleus. J. Physiol. 503 Pt. 2 (1997) 253-268
42. Sabatier N., Richard P., and Dayanithi G. Activation of multiple intracellular transduction signals by vasopressin in vasopressin-sensitive neurones of the rat supraoptic nucleus. J. Physiol. (London) 513 Pt. 3 (1998) 699-710
43. Sabatier N., Shibuya I., and Dayanithi G. Intracellular calcium increase and somatodendritic vasopressin release by vasopressin receptor agonists in the rat supraoptic nucleus: involvement of multiple intracellular transduction signals. J. Neuroendocrinol. 16 (2004) 221-236
44. Sajikumar S., Navakkode S., Sacktor T.C., and Frey J.U. Synaptic tagging and cross-tagging: the role of protein kinase Mzeta in maintaining long-term potentiation but not long-term depression. J. Neurosci. 25 (2005) 5750-5756
45. Serrano P., Yao Y., and Sacktor T.C. Persistent phosphorylation by protein kinase Mzeta maintains late-phase long-term potentiation. J. Neurosci. 25 (2005) 1979-1984
46. Shea T.B. Modulation of calpain-mediated protein kinase C activation within intact cells. Methods Mol. Biol. 144 (2000) 309-318
47. Shea T.B., Beermann M.L., Griffin W.R., and Leli U. Degradation of protein kinase C alpha and its free catalytic subunit, protein kinase M, in intact human neuroblastoma cells and under cell-free conditions. Evidence that PKM is degraded by mM calpain-mediated proteolysis at a faster rate than PKC. FEBS Lett. 350 (1994) 223-229
48. Shipston M.J., and Antoni F.A. Early glucocorticoid feedback in anterior pituitary corticotrophs: differential inhibition of hormone release induced by vasopressin and corticotrophin-releasing factor in vitro. J. Endocrinol. 129 (1991) 261-268
49. Son M.C., and Brinton R.D. Regulation and mechanism of L-type calcium channel activation via V1a vasopressin receptor activation in cultured cortical neurons. Neurobiol. Learn. Mem. 76 (2001) 388-402
50. Sulimovici S., Olmer A.J., and Carvounis C.P. Vasopressin stimulates translocation of protein kinase C in the toad urinary bladder. Exp. Nephrol. 4 (1996) 159-165
51. Sutton M.A., Bagnall M.W., Sharma S.K., Shobe J., and Carew T.J. Intermediate-term memory for site-specific sensitization in aplysia is maintained by persistent activation of protein kinase C. J. Neurosci. 24 (2004) 3600-3609
52. Takahashi T., Kimoto T., Tanabe N., Hattori T.A., Yasumatsu N., and Kawato S. Corticosterone acutely prolonged N-methyl-d-aspartate receptor-mediated Ca2+ elevation in cultured rat hippocampal neurons. J. Neurochem. 83 (2002) 1441-1451
53. Tan F.L., Lolait S.J., Brownstein M.J., Saito N., MacLeod V., Baeyens D.A., Mayeux P.R., Jones S.M., and Cornett L.E. Molecular cloning and functional characterization of a vasotocin receptor subtype that is expressed in the shell gland and brain of the domestic chicken. Biol. Reprod. 62 (2000) 8-15
54. Tanimura A., Nezu A., Morita T., Hashimoto N., and Tojyo Y. Interplay between calcium, diacylglycerol, and phosphorylation in the spatial and temporal regulation of PKCalpha-GFP. J. Biol. Chem. 277 (2002) 29054-29062
55. Touyarot K., Poussard S., Cortes-Torrea C., Cottin P., and Micheau J. Effect of chronic inhibition of calpains in the hippocampus on spatial discrimination learning and protein kinase C. Behav. Brain Res. 136 (2002) 439-448
56. Tripp S.K., and Moore F.L. Autoradiographic characterization of binding sites labelled with vasopressin in the brain of a urodele amphibian. Neuroendocrinology 48 (1988) 87-92
57. Zhao L., and Brinton R.D. Vasopressin-induced cytoplasmic and nuclear calcium signaling in cultured cortical astrocytes. Brain Res. 943 (2002) 117-131