Morphological basis of sensory neuropathy and neuroimmunomodulation in minor salivary glands of patients with Sjögren's syndrome

Archives of Oral Biology

Volumn 49, Issue 7, 2004, Pages 529-538

  Batbayar, B ^a   Nagy, G ^a   Kovesi G ^a   Zelles, T ^a   Feher E ^a  

^a SEMMELWEIS UNIVERSITY   (Hungary)

Author keywords

Immunocytes; Neuroimmunomodulation; Neuropeptides; Salivary glands; Sensory neuropathy; Sj gren's syndrome

Indexed keywords

GALANIN; NEUROPEPTIDE Y; NEUROPROTECTIVE AGENT; SUBSTANCE P; TYROSINE 3 MONOOXYGENASE; VASOACTIVE INTESTINAL POLYPEPTIDE;

ADULT; AGED; ARTICLE; ELECTRON MICROSCOPY; FEMALE; HUMAN; IMMUNOLOGY; IMMUNOMODULATION; LYMPHOCYTE; MALE; MAST CELL; MIDDLE AGED; MINOR SALIVA GLAND; NERVE FIBER; PATHOLOGY; PERIPHERAL NEUROPATHY; PLASMA CELL; SJOEGREN SYNDROME;

ADULT; AGED; FEMALE; GALANIN; HUMANS; LYMPHOCYTES; MALE; MAST CELLS; MICROSCOPY, ELECTRON; MIDDLE AGED; NERVE FIBERS; NEUROIMMUNOMODULATION; NEUROPEPTIDE Y; NEUROPROTECTIVE AGENTS; PERIPHERAL NERVOUS SYSTEM DISEASES; PLASMA CELLS; SALIVARY GLANDS, MINOR; SJOGREN'S SYNDROME; SUBSTANCE P; TYROSINE 3-MONOOXYGENASE; VASOACTIVE INTESTINAL PEPTIDE;

EID: 2342512177     PISSN: 00039969     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.archoralbio.2004.02.001     Document Type: Article

References (53)

1. Strand V., Talal N. Advances in the diagnosis and concept of Sjögren's syndrome (autoimmune exocrinopathy). Bull. Rheum. Dis. 30:1980;1046-1050
2. Moutsopoulos H.M. Sjögren's syndrome: autoimmune epithelitis (review). Clin. Immunol. Immunopathol. 72:1994;162-165
3. Lafitte C. Neuroradiological manifestations of primary Sjogren's syndrome. Revue Neurologique. 158:2002;959-965
4. Kaplan J.G., Rosenberg R., Reinitz E., Buchbinder S., Schaumburg H.H. Invited review: peripheral neuropathy in Sjogren's syndrome. Muscle Nerve. 13:1990;570-579
5. Chen W.H., Yeh J.H., Chiu H.C. Plasmapheresis in the treatment of ataxic sensory neuropathy associated with Sjogren's syndrome. Eur. Neurol. 45:2001;270-274
6. Urban P.P., Keilmann A., Teichmann E.M., Hopf H.C. Sensory neuropathy of the trigeminal, glossopharengeal, and vagal nerves in Sjogren's syndrome. J. Neurol. Sci. 186:2001;59-63
7. Grant I.A., Hunder G.G., Homburger H.A., Dyck P.J. Peripheral neuropathy associated with sicca complex. Neurology. 48:1997;855-862
8. Fehér E., Zelles T., Nagy G. Immunocytochemical localisation of neuropeptide-containing nerve fibres in human labial glands. Arch. Oral Biol. 44:1999;S33-S37
9. Konttinen Y.T., Sorsa T., Hukkanen M., Segerberg M., Kuhlefelt-Sundstrom M., Malmstrom M., et al. Topology of innervation of labial salivary glands by protein gene product 9.5 and synaptophysin immunoreactive nerves in patients with Sjogren's syndrome. J. Rheumatol. 19:1992;30-37
10. Tornwall J., Uusitalo H., Hukkanen M., Sorsa T., Konttinen Y.T. Distribution of vasoactive intestinal peptide (VIP) and its binding sites in labial salivary glands in Sjogren's syndrome and in normal controls. Clin. Exp. Rheum. 12:1994;287-292
11. Chrousos G.P. The hypothalamic-pituitary-adrenal axis and immune-mediated inflammation. N. Engl. J. Med. 332:1995;1351-1362
12. Kidd B.L., Mapp P.I., Blake D.R., Gibson S.J., Polak J.M. Neurogenic influences in arthritis. Ann. Rheum. Dis. 49:1990;649-652
13. Levine J.D., Collier D.H., Basbaum M.A., Moskowitz M.A., Helms C.A. Hypothesis: the nervous system may contribute to the pathophysiology of rheumatoid arthritis. J. Rheumatol. 12:1985;406-411
14. Levine J.D., Moskowith M.A., Basbaum A.I. The contribution of neurogenic inflammation in experimental arthritis. J. Immun. 135:1985;843-847
15. Levine J.D., Clark R., Devor M., Helms C., Moskowitz M.A., Basbaum A.I. Intraneuronal substance P contributes to the severity of experimental arthritis. Science. 226:1984;547-549
16. Louis S.M., Johnstone D., Russell A., Jamieson A., Dockray G.J. Antibodies to calcitonin gene-related peptide reduce inflammation induced by topical mustard oil but not to carrageenin in the rat. Neurosci. Lett. 102:1989;257-260
17. Bedoui S., Kawamura N., Straub R.H., Pabst R., Yamamura T., von Horsten S. Relevance of neuropeptide Y for the neuroimmune crosstalk (review). J. Neuroimmunol. 134:2003;1-11
18. Bijlsma J.W.J., Cutolo M., Masi A.T., Chikanza I.C. The neuroendocrine immune basis of rheumatic diseases. Immunol. Today. 20:1999;298-301
19. Gomariz R.P., Martinez C., Abad C., Leceta J., Delgado M. Immunology of VIP: a review and therapeutical perspectives. Curr. Pharm. Des. 7:2001;89-111
20. Vitali C., Bombardieri S., Jonsson R., Moutsopoulos H.M., Alexander E.L., Carsons S.E., et al. Classification criteria for Sjogren's syndrome: a revised version of the European criteria proposed by the American-European Consensus Group. Ann. Rheum. Dis. 61:2002;554-558
21. Santavirta N., Konttinen Y.T., Tornwall J., Segerberg M., Santavirta S., Matucci-Cerinic M., et al. Neuropeptides of the autonomic nervous system in Sjogren's syndrome. Ann. Rheum. Dis. 56:1990;737-740
22. Konttinen Y.T., Hukkanen M., Kemppinen P., Segerberg M., Sorsa T., Malmstrom M., et al. Peptide-containing nerves in labial salivary glands in Sjogren's syndrome. Arthritis Rheum. 35:1992;815-820
23. Fristad I. Dental innervation: functions and plasticity after peripheral injury (review). Acta Odontol. Scand. 55:1997;236-354
24. Elcock C., Boissonade F.M., Robinson P.P. Neuropeptide expression in the ferret trigeminal ganglion following ligation of the inferior alveolar nerve. Arch. Oral Biol. 46:2001;729-743
25. Lazarov N.E. Comparative analysis of the chemical neuroanatomy of the mammalian trigeminal ganglion and mesencephalic trigeminal nucleus. Prog. Neurobiol. 66:2002;19-59
26. Hou M., Uddman R., Tajti J., Edvinsson L. Nociceptin immunoreactivity and receptor mRNA in the human trigeminal ganglion. Brain Res. 964:2003;179-186
27. Mellgren S.I., Conn D.L., Stevens J.C., Dyck P.J. Peripheral neuropathy in primary Sjogren's syndrome. Neurology. 39:1989;390-394
28. Gemignani F., Marbini A., Pavesi G., Di Vittorio S., Manganelli P., Cenacchi G., et al. Peripheral neuropathy associated with primary Sjogren's syndrome. J. Neurol. Neurosurg. Psychiatr. 57:1994;983-986
29. Calza L., Pozza M., Zanni M., Manzini C.U., Manzini E., Hökfelt T. Peptide plasticity in primary sensory neurones and spinal cord during adjuvant-induced arthritis in the rat: an immunocytochemical and in situ hybridization study. Neuroscience. 82:1997;575-589
30. Shanahan F, Anton PA. Role of peptides in the regulation of the mucosal immune and inflammatory response. In: Walsh JH, Dockray GJ, editors. Gut peptides. New York: Raven Press; 1994.
31. Ottaway CA, Stanisz AM. Neural-immune interactions in the intestine: implications for inflammatory bowel disease. In: Kirsner JB, Shorter RG, editors. Inflammatory bowel disease. Baltimore: Williams and Wilkins; 1995.
32. Fehér E., Kovács Á., Gallatz K., Fehér J. Direct morphological evidence of neuroimmunomodulation in colonic mucosa of patients with Crohn's disease. Neuroimmunomodulation. 4:1997;250-257
33. Feher E., Altdorfer K., Bagameri G., Feher J. Neuroimmune interactions in experimental colitis. An immunoelectron microscopic study. Neuroimmunomodulation. 9:2001;247-255
34. Xing L.M., Guo J., Wand X. Induction and expression of beta-calcitonin gene-related peptide in rat T lymphocytes and its significance. J. Immunol. 165:2000;4359-4366
35. Gaytan F., Martinez-Fuentes A.J., Gracia-Navarro F., Vaudry H., Aguilar E. Pituitary adenylate cyclase activating peptide (PACAP) immunolocalization in lymphoid tissue of rat. Cell Tissue Res. 276:1994;233-237
36. Abad C., Martinez C., Leceta J., Juarranz M.G., Delgado M., Gomariz R.P. Pituitary adenylate-cyclase-activating polypeptide expression in the immune system. Neuroimmunomodulation. 10:2003;177-186
37. Delgado M., Abad C., Martinez C., Juarranz M.G., Leceta J., Ganea D., et al. PACAP in immunity and inflammation (review). Ann. N. Y. Acad. Sci. 992:2003;141-157
38. Lai J.P., Douglas S.D., Zhao M., Ho W.Z. Quantification of substance P mRNA in human mononuclear phagocytes and lymphocytes using a mimic-based PT-PCR. J. Immunol. Methods. 230:1999;149-157
39. Toyoda M., Makino T., Kagoura M., Morohashi M. Immunolocalization of substance P in human skin mast cells. Arch. Dermatol. Res. 292:2000;418-421
40. Stoyanova I.I., Gulubova M.V. Mast cells and inflammatory mediators in chronic ulcerative colitis. Acta Histochem. 104:2002;185-192
41. Li Y., Tian S., Douglas S.D., Ho W.Z. Morphine upregulates expression of substance P and its receptor in human blood mononuclear phagocytes and lymphocytes. Cell. Immunol. 205:2000;120-127
42. Bracci-Laudiero L., Aloe L., Stenfors C., Tirassa P., Theodorson E., Lundberg T. Nerve growth factor stimulates production of neuropeptide Y in human lymphocytes. NeuroReport. 7:1996;485-488
43. Amenta F., Bronzetti E., Cantalamessa F., El-Assouad D., Felici L., Ricci A., et al. Identification of dopamine plasma membrane and vesicular transporters in human peripheral blood lymphocytes. J. Neuroimmunol. 117:2001;133-142
44. McCormack R.J., Hart R.P., Ganea D. Expression of NK-1 receptor mRNA in murine lymphocytes. Neuroimmunomodulation. 3:1996;35-46
45. Kaltreider H.B., Ischikawa S., Byrd P.K., Ingram D.A., Kishiyama J.L., Sreedharan S.P., et al. Upregulation of neuropeptides and neuropeptide receptors in a murine model of immune inflammation in lung parenchyma. Am. J. Respir. Cell Mol. Biol. 16:1997;133-144
46. Mills C.D., Kincaid K., Alt J.M., Heilman M.J., Hill A.M. M-1/M-2 macrophages and the Th1/Th-2 paradigm. J. Immunol. 164:2000;6166-6173
47. Rothwell N.J. Cytokines - killers in the brain? J. Physiol. 514:1998;3-17
48. Rothwell N.J. Show them how it is really done. Nature. 405:2000;621
49. Martinez C., Delgado M., Abad C., Gomariz R.P., Ganea D., Leceta J. Regulation of VIP production and secretion by murine lymphocytes. J. Neuroimmunol. 93:1999;126-138
50. Konttinen Y.T., Hietanen J., Virtanen I., Ma J., Sorsa T., Xu W., et al. Mast cell derangement in salivary glands in patients with Sjogren's syndrome. Rheumatol. Int. 19:2000;141-147
51. Syrjänen S.M., Syrjänen K.J. Mast cells in the labial salivary glands of patients suffering from rheumatoid arthritis. Scand. J. Dent. Res. 92:1984;557-563
52. Syrjänen S.M., Syrjänen K.J. Inflammatory cell infiltrate in labial salivary glands of patients with rheumatoid arthritis with special emphasis on tissue mast cells. Scand. J. Dent. Res. 92:1984;557-563
53. Skopouli F.N., Li L., Boumba D., Stefanaki S., Hanel K., Moutsopoulos H.M., et al. Association of mast cells with fibrosis and fatty infiltration in the minor salivary glands of patients with Sjogren's syndrome. Clin. Exp. Rheumatol. 16:1998;63-65