PACAP-cytokine interactions govern adrenal neuropeptide biosynthesis after systemic administration of LPS

Neuropharmacology

Volumn 58, Issue 1, 2010, Pages 208-214

  Ait Ali, Djida ^a   Stroth, Nikolas ^a   Sen, Jyoti M ^b   Eiden, Lee E ^a  

^a NATIONAL INSTITUTE OF MENTAL HEALTH   (United States)

^b NATIONAL INSTITUTE ON AGING   (United States)

Author keywords

Adrenal cortex; Adrenal medulla; Galanin; LPS; PACAP; Septic shock; Stress; TNF alpha; VIP

Indexed keywords

CYTOKINE; GALANIN; HYPOPHYSIS ADENYLATE CYCLASE ACTIVATING POLYPEPTIDE; I KAPPA B ALPHA; LIPOPOLYSACCHARIDE; MESSENGER RNA; NEUROPEPTIDE; TUMOR NECROSIS FACTOR ALPHA; VASOACTIVE INTESTINAL POLYPEPTIDE;

ADRENAL CORTEX; ADRENAL MEDULLA; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; AUTOREGULATION; CHROMAFFIN CELL; CONTROLLED STUDY; CYTOKINE PRODUCTION; DOWNSTREAM PROCESSING; GENE INDUCTION; IMMUNE RESPONSE; IN VIVO STUDY; MALE; MOUSE; NONHUMAN; PEPTIDE SYNTHESIS; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN PROTEIN INTERACTION; SEPTIC SHOCK; SIGNAL TRANSDUCTION; SPLANCHNIC NERVE; STEROIDOGENESIS; STRESS; UPREGULATION;

ADRENAL GLANDS; ANALYSIS OF VARIANCE; ANIMALS; CATTLE; CELLS, CULTURED; CHROMAFFIN CELLS; CYTOKINES; DRUG SYNERGISM; GALANIN; LIPOPOLYSACCHARIDES; MICE; MICE, INBRED C57BL; MICE, KNOCKOUT; NEUROPEPTIDES; PITUITARY ADENYLATE CYCLASE-ACTIVATING POLYPEPTIDE; TUMOR NECROSIS FACTOR-ALPHA; UP-REGULATION; VASOACTIVE INTESTINAL PEPTIDE;

EID: 71549124313     PISSN: 00283908     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neuropharm.2009.07.034     Document Type: Article

References (40)

1. Ait-Ali D., Turquier V., Grumolato L., Yon L., Jourdain M., Alexandre D., Eiden L.E., Vaudry H., and Anouar Y. The proinflammatory cytokines tumor necrosis factor-alpha and interleukin-1 stimulate neuropeptide gene transcription and secretion in adrenochromaffin cells via activation of extracellularly regulated kinase 1/2 and p38 protein kinases, and activator protein-1 transcription factors. Mol. Endocrinol. 18 (2004) 1721-1739
2. Ait-Ali D., Turquier V., Tanguy Y., Thouennon E., Ghzili H., Mounien L., Derambure C., Jegou S., Salier J.P., Vaudry H., Eiden L.E., and Anouar Y. Tumor necrosis factor (TNF)-alpha persistently activates nuclear factor-kappaB signaling through the type 2 TNF receptor in chromaffin cells: implications for long-term regulation of neuropeptide gene expression in inflammation. Endocrinology 149 (2008) 2840-2852
3. Andreis P.G., Tortorella C., Ziolkowska A., Spinazzi R., Malendowicz L.K., Neri G., and Nussdorfer G.G. Evidence for a paracrine role of endogenous adrenomedullary galanin in the regulation of glucocorticoid secretion in the rat adrenal gland. Int. J. Mol. Med. 19 (2007) 511-515
4. Anouar Y., MacArthur L., Cohen J., Iacangelo A.L., and Eiden L.E. Identification of a TPA-responsive element mediating preferential transactivation of the galanin gene promoter in chromaffin cells. J. Biol. Chem. 269 (1994) 6823-6831
5. Arranz A., Androulidaki A., Zacharioudaki V., Martinez C., Margioris A.N., Gomariz R.P., and Tsatsanis C. Vasoactive intestinal peptide suppresses toll-like receptor 4 expression in macrophages via Akt1 reducing their responsiveness to lipopolysaccharide. Mol. Immunol. 45 (2008) 2970-2980
6. Bornstein S.R., Haidan A., and Ehrhart-Bornstein M. Cellular communication in the neuro-adrenocortical axis: role of vasoactive intestinal polypeptide (VIP). Endocr. Res. 22 (1996) 819-829
7. Brenneman D.E. Neuroprotection: a comparative view of vasoactive intestinal peptide and pituitary adenylate cyclase-activating polypeptide. Peptides 28 (2007) 1720-1726
8. Chomczynski P., and Sacchi N. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal. Biochem. 162 (1987) 156-159
9. Ehrhart-Bornstein M., Bornstein S.R., Scherbaum W.A., Pfeiffer E.F., and Holst J.J. Role of the vasoactive intestinal peptide in a neuroendocrine regulation of the adrenal cortex. Neuroendocrinology 54 (1991) 623-628
10. Elenkov I.J., Chrousos G.P., and Wilder R.L. Neuroendocrine regulation of IL-12 and TNF-alpha/IL-10 balance. Clinical implications. Ann. N Y Acad. Sci. 917 (2000) 94-105
11. Eskay R.L., and Eiden L.E. Interleukin-1 alpha and tumor necrosis factor-alpha differentially regulate enkephalin, vasoactive intestinal polypeptide, neurotensin, and substance P biosynthesis in chromaffin cells. Endocrinology 130 (1992) 2252-2258
12. Fischer-Colbrie R., Eskay R.L., Eiden L.E., and Maas D. Transsynaptic regulation of galanin, neurotensin, and substance P in the adrenal medulla: combinatorial control by second-messenger signaling pathways. J. Neurochem. 59 (1992) 780-783
13. Fischer-Colbrie R., Kirchmair R., Kahler C.M., Wiedermann C.J., and Saria A. Secretoneurin: a new player in angiogenesis and chemotaxis linking nerves, blood vessels and the immune system. Curr. Protein Pept. Sci. 6 (2005) 373-385
14. Goetzl E.J., Chan R.C., and Yadav M. Diverse mechanisms and consequences of immunoadoption of neuromediator systems. Ann. N Y Acad. Sci. 1144 (2008) 56-60
15. Hamelink C., Tjurmina O., Damadzic R., Young W.S., Weihe E., Lee H.W., and Eiden L.E. Pituitary adenylate cyclase-activating polypeptide is a sympathoadrenal neurotransmitter involved in catecholamine regulation and glucohomeostasis. Proc. Natl. Acad. Sci. U.S.A. 99 (2002) 461-466
16. Imler J.L., and Zheng L. Biology of Toll receptors: lessons from insects and mammals. J. Leukoc. Biol. 75 (2004) 18-26
17. Ito C.Y., Kazantsev A.G., and Baldwin Jr. A.S. Three NF-kappa B sites in the I kappa B-alpha promoter are required for induction of gene expression by TNF alpha. Nucleic Acids Res. 22 (1994) 3787-3792
18. Kanamatsu T., Unsworth C.D., Diliberto Jr. E.J., Viveros O.H., and Hong J.S. Reflex splanchnic nerve stimulation increases levels of proenkephalin A mRNA and proenkephalin A-related peptides in the rat adrenal medulla. Proc. Natl. Acad. Sci. U.S.A. 83 (1986) 9245-9249
19. Lee E.G., Boone D.L., Chai S., Libby S.L., Chien M., Lodolce J.P., and Ma A. Failure to regulate TNF-induced NF-kappaB and cell death responses in A20-deficient mice. Science 289 (2000) 2350-2354
20. Li M., David C., Kikuta T., Somogyvari-Vigh A., and Arimura A. Signaling cascades involved in neuroprotection by subpicomolar pituitary adenylate cyclase-activating polypeptide 38. J. Mol. Neurosci. 27 (2005) 91-105
21. Lipniacki T., Paszek P., Brasier A.R., Luxon B., and Kimmel M. Mathematical model of NF-kappaB regulatory module. J. Theor. Biol. 228 (2004) 195-215
22. Mahata S.K., Mahata M., Livsey Taylor C.V., Taupenot L., Parmer R.J., and O'Connor D.T. The novel catecholamine release-inhibitory peptide catestatin (chromogranin A344-364). Properties and function. Adv. Exp. Med. Biol. 482 (2000) 263-277
23. Misch E.A., and Hawn T.R. Toll-like receptor polymorphisms and susceptibility to human disease. Clin. Sci. (Lond) 114 (2008) 347-360
24. Oguri S., Motegi K., Iwakura Y., and Endo Y. Primary role of interleukin-1 alpha and interleukin-1 beta in lipopolysaccharide-induced hypoglycemia in mice. Clin. Diagn. Lab. Immunol. 9 (2002) 1307-1312
25. Papadakis K.A., and Targan S.R. Tumor necrosis factor: biology and therapeutic inhibitors. Gastroenterology 119 (2000) 1148-1157
26. Perez-Rodriguez R., Roncero C., Olivan A.M., Gonzalez M.P., and Oset-Gasque M.J. Signaling mechanisms of interferon gamma induced apoptosis in chromaffin cells: involvement of nNOS, iNOS, and NFkappaB. J. Neurochem. 108 (2009) 1083-1096
27. Qi M., Zhou Z.Z., Wurster R.D., and Jones S.B. Mechanisms involved in the rapid dissipation of plasma epinephrine response to bacterial endotoxin in conscious rats. Am. J. Physiol. 261 (1991) R1431-R1437
28. Quintana F.J., Zaltzman R., Fernandez-Montesinos R., Herrera J.L., Gozes I., Cohen I.R., and Pozo D. NAP, a peptide derived from the activity-dependent neuroprotective protein, modulates macrophage function. Ann. N Y Acad. Sci. 1070 (2006) 500-506
29. Stroth N., Hamelink C., and Eiden L.E. PACAP-dependent cellular plasticity in the mouse adrenal gland. FASEB J. 21 (2007) A1249-A1250
30. Su Y., Ganea D., Peng X., and Jonakait G.M. Galanin down-regulates microglial tumor necrosis factor-alpha production by a post-transcriptional mechanism. J. Neuroimmunol 134 (2003) 52-60
31. Sun S.C., Ganchi P.A., Ballard D.W., and Greene W.C. NF-kappa B controls expression of inhibitor I kappa B alpha: evidence for an inducible autoregulatory pathway. Science 259 (1993) 1912-1915
32. Tai T.C., Claycomb R., Siddall B.J., Bell R.A., Kvetnansky R., and Wong D.L. Stress-induced changes in epinephrine expression in the adrenal medulla in vivo. J. Neurochem. 101 (2007) 1108-1118
33. Takeda K., and Akira S. Toll-like Receptors. Curr Protoc Immunol (2007) (Chapter 14) Unit 14 12
34. Takeda K., Kaisho T., and Akira S. Toll-like receptors. Annu. Rev. Immunol. 21 (2003) 335-376
35. Tonshoff C., Hemmick L., and Evinger M.J. Pituitary adenylate cyclase activating polypeptide (PACAP) regulates expression of catecholamine biosynthetic enzyme genes in bovine adrenal chromaffin cells. J. Mol. Neurosci. 9 (1997) 127-140
36. Ulloa L., and Tracey K.J. The "cytokine profile": a code for sepsis. Trends Mol. Med. 11 (2005) 56-63
37. Wong D.L., and Tank A.W. Stress-induced catecholaminergic function: transcriptional and post-transcriptional control. Stress 10 (2007) 121-130
38. Yadav M., and Goetzl E.J. Vasoactive intestinal peptide-mediated Th17 differentiation: an expanding spectrum of vasoactive intestinal peptide effects in immunity and autoimmunity. Ann. N Y Acad. Sci. 1144 (2008) 83-89
39. Zacharowski K., Zacharowski P.A., Koch A., Baban A., Tran N., Berkels R., Papewalis C., Schulze-Osthoff K., Knuefermann P., Zahringer U., Schumann R.R., Rettori V., McCann S.M., and Bornstein S.R. Toll-like receptor 4 plays a crucial role in the immune-adrenal response to systemic inflammatory response syndrome. Proc. Natl. Acad. Sci. U.S.A. 103 (2006) 6392-6397
40. Zhou X.F., and Livett B.G. Substance P has biphasic effects on catecholamine secretion evoked by electrical stimulation of perfused rat adrenal glands in vitro. J. Auton. Nerv Syst. 31 (1990) 31-39