Pineal arylalkylamine N-acetyltransferase (Aanat) gene expression as a target of inflammatory mediators in the chicken

General and Comparative Endocrinology

Volumn 179, Issue 2, 2012, Pages 143-151

  Piesiewicz, Aneta ^a   Kedzierska, Urszula ^a   Adamska, Iwona ^a   Usarek, Michal ^a   Zeman, Michal ^b   Skwarlo Sonta, Krystyna ^a   Majewski, Pawel Marek ^a  

^a UNIVERSITY OF WARSAW   (Poland)

^b Faculty of Natural Sciences   (Slovakia)

Author keywords

AANAT; Chickens; Inflammation; Melatonin biosynthesis; Pineal gland

Indexed keywords

ARALKYLAMINE ACETYLTRANSFERASE; MELATONIN; MESSENGER RNA; N ACETYLSEROTONIN; THIOGLYCOLIC ACID; ACETYLSEROTONIN METHYLTRANSFERASE; ACYLTRANSFERASE; AROMATIC LEVO AMINO ACID DECARBOXYLASE; AUTACOID; PROTEIN 14 3 3; DRUG DERIVATIVE; N-ACETYLSEROTONIN; SEROTONIN; THIOGLYCOLIC ACID DERIVATIVE; TRYPTOPHAN HYDROXYLASE;

AANAT GENE; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; ASMT GENE; BIOSYNTHESIS; CHICKEN; CONTROLLED STUDY; DDC GENE; ENZYME ACTIVITY; ENZYME SYNTHESIS; GENE EXPRESSION; HORMONE BLOOD LEVEL; INFLAMMATION; MALE; NIGHT; NONHUMAN; NUCLEOTIDE SEQUENCE; PERITONITIS; PINEAL BODY; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; TPH1 GENE; TRANSCRIPTION REGULATION; ACETYLSEROTONIN O METHYLTRANSFERASE GENE; ARYLALKYLAMINE N ACETYLTRANSFERASE GENE; CIRCADIAN RHYTHM; DOPA DECARBOXYLASE GENE; DOWN REGULATION; ENZYME INHIBITION; GENE; HORMONE SYNTHESIS; N ACETYLTRANSFERASE GENE; TRYPTOPHAN HYDROXYLASE 1 GENE; ANIMAL; CHEMICALLY INDUCED DISORDER; DRUG EFFECT; ENZYMOLOGY; GENETICS; METABOLISM; PATHOPHYSIOLOGY; PHYSIOLOGY;

ACETYLSEROTONIN O-METHYLTRANSFERASE; ANIMALS; ARYLALKYLAMINE N-ACETYLTRANSFERASE; CHICKENS; CIRCADIAN RHYTHM; DOPA DECARBOXYLASE; DOWN-REGULATION; INFLAMMATION MEDIATORS; MALE; MELATONIN; PERITONITIS; PINEAL GLAND; RNA, MESSENGER; SEROTONIN; THIOGLYCOLATES; TRYPTOPHAN HYDROXYLASE;

EID: 84866265610     PISSN: 00166480     EISSN: 10956840     Source Type: Journal    
DOI: 10.1016/j.ygcen.2012.08.013     Document Type: Article

References (61)

1. Aitken A. 14-3-3 And its possible role in co-ordinating multiple signalling pathways. Trends Cell Biol. 1996, 6:341-347.
2. Atanassova P.A., Terzieva D.D., Dimitrov B.D. Impaired nocturnal melatonin in acute phase of ischaemic stroke: cross-sectional matched case-control analysis. J. Neuroendocrinol. 2009, 21:657-663.
3. Bailey M.J., Beremand P.D., Hammer R., Bell-Pedersen D., Thomas T.L., Cassone V.M. Transcriptional profiling of the chick pineal gland, a photoreceptive circadian oscillator and pacemaker. Mol. Endocrinol. 2003, 17:2084-2095.
4. Barbosa R., Scialfa J.H., Terra I.M., Cipolla-Neto J., Simonneaux V., Afeche S.C. Tryptophan hydroxylase is modulated by L-type calcium channels in the rat pineal gland. Life Sci. 2008, 82:529-535.
5. Barriga C., Marchena J.M., Lea R.W., Harvey S., Rodriguez A.B. Effect of stress and dexamethasone treatment on circadian rhythms of melatonin and corticosterone in ring dove (Streptopelia risoria). Mol. Cell. Biochem. 2002, 232:27-31.
6. Bell-Pedersen D., Cassone V.M., Earnest D.J., Golden S.S., Hardin P.E., Thomas T.L., et al. Circadian rhythms from multiple oscillators: lessons from diverse organisms. Nat. Rev. Genet. 2005, 6:544-556.
7. Borjigin J., Zhang L.S., Calinescu A.A. Circadian regulation of pineal gland rhythmicity. Mol. Cell. Endocrinol. 2012, 349:13-19.
8. Cagnacci A., Soldani R., Romagnolo C., Yen S.S. Melatonin-induced decrease of body temperature in women: a threshold event. Neuroendocrinology 1994, 60:549-552.
9. Carvalho-Sousa C.E., Cruz-Machado S.S., Tamura E.K., Pedro A.C., Fernandes M., Pinato L., et al. Molecular basis for defining the pineal gland and pinealocytes as targets for tumor necrosis factor. Front. Endocrinol. 2011, 2:1-11.
10. Cassone V.M. Melatonin's role in vertebrate circadian rhythms. Chronobiol. Int. 1998, 15:457-473.
11. Cecon E., Fernandes P.A., Pinato L., Ferreira Z.S., Markus R.P. Daily variation of constitutively activated nuclear factor kappa B (NFKB) in rat pineal gland. Chronobiol. Int. 2010, 27:52-67.
12. Chae H.D., Park T.J., Lee Y.K., Lee T.G., Kim K.T. Rapid and simple measurement of serotonin N-acetyltransferase activity by liquid biphasic diffusion assay. Neurochem. Int. 1999, 35:447-451.
13. Couto-Moraes R., Palermo-Neto J., Markus R.P. The immune-pineal axis: stress as a modulator of pineal gland function. Ann. N. Y. Acad. Sci. 2009, 1153:193-202.
14. Cronin A.J., Keifer J.C., Davies M.F., King T.S., Bixler E.O. Melatonin secretion after surgery. Lancet 2000, 356:1244-1245.
15. Da Silveira Cruz-Machado S., Carvalho-Sousa C.E., Tamura E.K., Pinato L., Cecon E., Fernandes P.A., et al. TLR4 and CD14 receptors expressed in rat pineal gland trigger NFKB pathway. J. Pineal Res. 2010, 49:183-192.
16. Da Silveira Cruz-Machado S., Pinato L., Tamura E.K., Carvalho-Sousa C.E., Markus R.P. Glia-pinealocyte network: the paracrine modulation of melatonin synthesis by tumor necrosis factor (TNF). PLoS ONE 2012, 7:e40142.
17. Fernandes P.A., Bothorel B., Clesse D., Monteiro A.W., Calgari C., Raison S., et al. Local corticosterone infusion enhances nocturnal pineal melatonin production in vivo. J. Neuroendocrinol. 2009, 21:90-97.
18. Fernandes P.A., Cecon E., Markus R.P., Ferreira Z.S. Effect of TNF-alpha on the melatonin synthetic pathway in the rat pineal gland: basis for a 'feedback' of the immune response on circadian timing. J. Pineal Res. 2006, 41:344-350.
19. Ferreira Z.S., Bothorel B., Markus R.P., Simonneaux V. Plasma corticosterone elevation inhibits the activation of nuclear factor kappa B (NFKB) in the Syrian hamster pineal gland. Stress 2012, 15:339-347.
20. Ferreira Z.S., Fernandes P.A., Duma D., Assreuy J., Avellar M.C., Markus R.P. Corticosterone modulates noradrenaline-induced melatonin synthesis through inhibition of nuclear factor kappa B. J. Pineal Res. 2005, 38:182-188.
21. Ganguly S., Coon S.L., Klein D.C. Control of melatonin synthesis in the mammalian pineal gland: the critical role of serotonin acetylation. Cell Tissue Res. 2002, 309:127-137.
22. Ganguly S., Gastel J.A., Weller J.L., Schwartz C., Jaffe H., Namboodiri M.A., et al. Role of a pineal cAMP-operated arylalkylamine N-acetyltransferase/14-3-3-binding switch in melatonin synthesis. Proc. Natl. Acad. Sci. USA 2001, 98:8083-8088.
23. Ganguly S., Weller J.L., Ho A., Chemineau P., Malpaux B., Klein D.C. Melatonin synthesis: 14-3-3-dependent activation and inhibition of arylalkylamine N-acetyltransferase mediated by phosphoserine-205. Proc. Natl. Acad. Sci. USA 2005, 102:1222-1227.
24. Guerrero J.M., Reiter R.J. Melatonin-immune system relationships. Curr. Top. Med. Chem. 2002, 2:167-179.
25. Guo X., Kuzumi E., Charman S.C., Vuylsteke A. Perioperative melatonin secretion in patients undergoing coronary artery bypass grafting. Anesth. Analg. 2002, 94:1085-1091.
26. Hong Y.H., Lillehoj H.S., Lee S.H., Dalloul R.A., Lillehoj E.P. Analysis of chicken cytokine and chemokine gene expression following Eimeria acervulina and Eimeria tenella infections. Vet. Immunol. Immunopathol. 2006, 114:209-223.
27. Hyland K., Clayton P.T. Aromatic l-amino acid decarboxylase deficiency: diagnostic methodology. Clin. Chem. 1992, 38:2405-2410.
28. Jiang-Shieh Y.F., Wu C.H., Chien H.F., Wei I.H., Chang M.L., Shieh J.Y., et al. Reactive changes of interstitial glia and pinealocytes in the rat pineal gland challenged with cell wall components from Gram-positive and -negative bacteria. J. Pineal Res. 2005, 38:17-26.
29. Kaiser P., Wu Z., Rothwell L., Fife M., Gibson M., Poh T.Y., et al. Prospects for understanding immune-endocrine interactions in the chicken. Gen. Comp. Endocrinol. 2009, 163:83-91.
30. Karkela J., Vakkuri O., Kaukinen S., Huang W.Q., Pasanen M. The influence of anaesthesia and surgery on the circadian rhythm of melatonin. Acta Anaesthesiol. Scand. 2002, 46:30-36.
31. Klein D.C., Ganguly S., Coon S., Weller J.L., Obsil T., Hickman A., et al. 14-3-3 Proteins and photoneuroendocrine transduction: role in controlling the daily rhythm in melatonin. Biochem. Soc. Trans. 2002, 30:365-373.
32. Logan R.W., Sarkar D.K. Circadian nature of immune function. Mol. Cell. Endocrinol. 2012, 349:82-90.
33. Ludemann P., Zwernemann S., Lerchl A. Clearance of melatonin and 6-sulfatoxymelatonin by hemodialysis in patients with end-stage renal disease. J. Pineal Res. 2001, 31:222-227.
34. Majewski P., Adamska I., Pawlak J., Baranska A., Skwarlo-Sonta K. Seasonality of pineal gland activity and immune functions in chickens. J. Pineal Res. 2005, 39:66-72.
35. Majewski P., Dziwinski T., Pawlak J., Waloch M., Skwarlo-Sonta K. Anti-inflammatory and opioid-mediated effects of melatonin on experimental peritonitis in chickens. Life Sci. 2005, 76:1907-1920.
36. Majewski P., Markowska M., Laskowska H., Waloch M., Skwarlo-Sonta K. Effect of morphine on thioglycollate-induced peritonitis in chickens. Neuro Endocrinol. Lett. 2002, 23:161-167.
37. Markowska M., Bialecka B., Ciechanowska M., Koter Z., Laskowska H., Karkucinska-Wieckowska A., et al. Effect of immunization on nocturnal NAT activity in chicken pineal gland. Neuro Endocrinol. Lett. 2000, 21:367-373.
38. Markus R.P., Ferreira Z.S. The immune-pineal axis: the role of pineal and extra-pineal melatonin in modulating inflammation. Adv. Neuroimmune Biol. 2011, 1:95-104.
39. Markus R.P., Ferreira Z.S., Fernandes P.A., Cecon E. The immune-pineal axis: a shuttle between endocrine and paracrine melatonin sources. NeuroImmunoModulation 2007, 14:126-133.
40. Mucha S., Zylinska K., Zerek-Melen G., Swietoslawski J., Stepien H. Effect of interleukin-1 on in vivo melatonin secretion by the pineal gland in rats. Adv. Pineal Res. 1994, 7:177-181.
41. Nishimura S., Fujino Y., Shimaoka M., Hagihira S., Taenaka N., Yoshiya I. Circadian secretion patterns of melatonin after major surgery. J. Pineal Res. 1998, 25:73-77.
42. Obsil T., Ghirlando R., Klein D.C., Ganguly S., Dyda F. Crystal structure of the 14-3-3zeta:serotonin N-acetyltransferase complex: a role for scaffolding in enzyme regulation. Cell 2001, 105:257-267.
43. Olszanska B., Majewski P., Lewczuk B., Stepinska U. Melatonin and its synthesizing enzymes (arylalkylamine N-acetyltransferase-like and hydroxyindole-O-methyltransferase) in avian eggs and early embryos. J. Pineal Res. 2007, 42:310-318.
44. Pang S.F., Li L., Ayre E.A., Pang C.S., Lee P.P., Xu R.K., et al. Neuroendocrinology of melatonin in reproduction: recent developments. J. Chem. Neuroanat. 1998, 14:157-166.
45. A. Piesiewicz, U. Kedzierska, E. Podobas, I. Adamska, K. Zuzewicz, P.M. Majewski, Season-dependent postembryonic maturation of the diurnal rhythm of melatonin biosynthesis in the chicken pineal gland. Chronobiol. Int. (2012), http://dx.doi.org/10.3109/07420528.2012.719964.
46. Piesiewicz A., Podobas E., Keogonekdzierska U., Joachimiak E., Markowska M., Majewski P., et al. Season-related differences in the biosynthetic activity of the neonatal chicken pineal gland. Open Ornithol. J. 2010, 3:134-140.
47. Pontes G.N., Cardoso E.C., Carneiro-Sampaio M.M., Markus R.P. Injury switches melatonin production source from endocrine (pineal) to paracrine (phagocytes) - melatonin in human colostrum and colostrum phagocytes. J. Pineal Res. 2006, 41:136-141.
48. Pontes G.N., Cardoso E.C., Carneiro-Sampaio M.M., Markus R.P. Pineal melatonin and the innate immune response: the TNF-alpha increase after cesarean section suppresses nocturnal melatonin production. J. Pineal Res. 2007, 43:365-371.
49. Ribelayga C., Pevet P., Simonneaux V. HIOMT drives the photoperiodic changes in the amplitude of the melatonin peak of the Siberian hamster. Am. J. Physiol. Regul. Integr. Comp. Physiol. 2000, 278:R1339-R1345.
50. Simonneaux V., Ribelayga C. Generation of the melatonin endocrine message in mammals: a review of the complex regulation of melatonin synthesis by norepinephrine, peptides, and other pineal transmitters. Pharmacol. Rev. 2003, 55:325-395.
51. Skwarlo-Sonta K. Melatonin in immunity: comparative aspects. Neuro Endocrinol. Lett. 2002, 23(Suppl. 1):61-66.
52. Skwarlo-Sonta K., Majewski P., Markowska M., Jakubowska A., Waloch M. Bimodal effects of melatonin on the inflammatory reaction in young chickens. Treatise on Pineal Gland and Melatonin 2002, 225-238. Science Publishers, Enfield (NH), USA Plymouth, UK. C. Haldar, M. Singaravel, S. Maitra (Eds.).
53. Skwarlo-Sonta K., Majewski P., Markowska M., Oblap R., Olszanska B. Bidirectional communication between the pineal gland and the immune system. Can. J. Physiol. Pharmacol. 2003, 81:342-349.
54. Tamura E.K., Fernandes P.A., Marcola M., Da Silveira Cruz-Machado S., Markus R.P. Long-lasting priming of endothelial cells by plasma melatonin levels. PLoS ONE 2010, 5:e13958.
55. Tan D.X., Manchester L.C., Terron M.P., Flores L.J., Reiter R.J. One molecule, many derivatives: a never-ending interaction of melatonin with reactive oxygen and nitrogen species?. J. Pineal Res. 2007, 42:28-42.
56. Underwood H., Steele C.T., Zivkovic B. Circadian organization and the role of the pineal in birds. Microsc. Res. Tech. 2001, 53:48-62.
57. Vasto S., Candore G., Balistreri C.R., Caruso M., Colonna-Romano G., Grimaldi M.P., et al. Inflammatory networks in ageing, age-related diseases and longevity. Mech. Ageing Dev. 2007, 128:83-91.
58. Withyachumnarnkul B., Nonaka K.O., Santana C., Attia A.M., Reiter R.J. Interferon-gamma modulates melatonin production in rat pineal glands in organ culture. J. Interferon Res. 1990, 10:403-411.
59. Zawilska J.B., Skene D.J., Arendt J. Physiology and pharmacology of melatonin in relation to biological rhythms. Pharmacol. Rep. 2009, 61:383-410.
60. Zeman M., Gwinner E., Herichova I., Lamosova D., Kost'al L. Perinatal development of circadian melatonin production in domestic chicks. J. Pineal Res. 1999, 26:28-34.
61. Zeman M., Herichova I. Circadian melatonin production develops faster in birds than in mammals. Gen. Comp. Endocrinol. 2011, 172:23-30.