Altered expression of MUC2 and MUC5AC in response to Shigella infection, an in vivo study

Biochimica et Biophysica Acta - General Subjects

Volumn 1770, Issue 6, 2007, Pages 884-889

  Radhakrishnan, Prakash ^a   Halagowder, Devaraj ^a   Devaraj, S Niranjali ^a  

^a UNIVERSITY OF MADRAS   (India)

Author keywords

Ileal loop ligation assay; MUC2; MUC5AC; Shigella species; Shigellosis

Indexed keywords

MITOGEN ACTIVATED PROTEIN KINASE 1; MITOGEN ACTIVATED PROTEIN KINASE 3; MUCIN 2; MUCIN 5AC; PROTEIN KINASE C; TUMOR NECROSIS FACTOR ALPHA;

ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; CONTROLLED STUDY; ENTERITIS; IN VIVO STUDY; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; RABBIT; SHIGELLA; SHIGELLOSIS; SIGNAL TRANSDUCTION; UPREGULATION;

ANIMALS; DIARRHEA; DYSENTERY, BACILLARY; EPITHELIAL CELLS; HUMANS; INFLAMMATORY BOWEL DISEASES; INTESTINAL MUCOSA; MITOGEN-ACTIVATED PROTEIN KINASE 1; MITOGEN-ACTIVATED PROTEIN KINASE 3; MUCINS; PROTEIN KINASE C; RABBITS; SHIGELLA DYSENTERIAE; SHIGELLA FLEXNERI; TIME FACTORS; TUMOR NECROSIS FACTOR-ALPHA; UP-REGULATION;

SHIGELLA;

EID: 34247219571     PISSN: 03044165     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbagen.2007.01.019     Document Type: Article

References (31)

1. Sur D., Ramamurthy T., Deen J., and Bhattacharya S.K. Shigellosis: challenges and management issues. Indian J. Med. Res. 120 (2004) 454-462
2. DuPont H.L. Shigella species (Bacillary dysentery). In: Mandell G.L.S., Douglas Jr. R.G., and Bennet J.E. (Eds). Principles and Practice of Infectious Disease (1990), Churchill Livingstone 1716-1722
3. Stoll B.J., Glass R.I., Huq M.I., Khan M.U., Banu H., and Holt J. Epidemiologic and clinical features of patients infected with Shigella who attended a diarrhoeal disease hospital in Bangladesh. J. Infect. Dis. 146 (1982) 177-183
4. Rahman M.M., and Wahed M.M. Direct nutrition loss and Diarrhoea. In: Chen L.S., and Crimshaw L.S. (Eds). Diarrhoea and Malnutrition (1983), Plenum, New York 155-160
5. Angulo F.J., and Swerdlow D.L. Bacterial enteric infections in persons infected with HIV. Clin. Infect. Dis. 21 (1995) S84-S93
6. Takeuchi A.M., Spring H., Labrec E.H., and Formal S.B. Experimental bacillary dysentery: an electron microscopic study of the response of the intestinal mucosa to bacterial invasion. Am. J. Pathol. 47 (1965) 1011-1044
7. Hollingsworth M.A., and Swanson B.J. Mucins in cancer: protection and control of the cell surface. Nat. Rev., Cancer 4 (2004) 45-60
8. Moniaux N., Andrianifahanana M., Brand R.E., and Batra S.K. Multiple roles of mucins in pancreatic cancer, a lethal and challenging malignancy. Br. J. Cancer 91 (2004) 1633-1638
9. Weiss A.A., Babyatsky M.W., Ogata S., Chen A., and Itzkowitz S.H. Expression of MUC2 and MUC3 mRNA in human normal, malignant, and inflammatory intestinal tissues. J. Histochem. Cytochem. 44 (1996) 1161-1166
10. Nutten S., Sansonetti P., Huet G., Bisiaux C.B., Meresse B., Colombel J.F., and Desreumaux P. Epithelial inflammation response induced by Shigella flexneri depends on mucin gene expression. Microbes Infect. 4 (2002) 1121-1124
11. Bartman E., Sanderson S.J., Ewing S.L., Niehans G.A., Wiehr C.L., Evans M.K., and Ho S.B. Aberrant expression of MUC5AC and MUC6 gastric mucin genes in colorectal polyps. Int. J. Cancer 80 (1999) 210-221
12. Krunkosky T.M., Fischer B.M., Martin L.D., Jones N., Akely N.J., and Adler K.B. Effects of TNFα on expression of ICAM-1 in human airway epithelial cells in vitro, signaling pathways controlling surface and gene expression. Am. J. Respir. Cell Mol. Biol. 22 (2000) 685-692
13. Levine S.J., Larivee P., Logun C., Angus C.W., Ognibene F.P., and Shelhamer J.H. Tumor necrosis factor-alpha induces mucin hyper secretion and MUC-2 gene expression by human airway epithelial cells. Am. J. Respir. Cell Mol. Biol. 12 (1995) 196-204
14. Dohrman S., Miyata M., Gallup M., Li J.D., Chapelin C., Coste A., Escudier E., Nadel J., and Basbaum C. Mucin gene (MUC2 and MUC5AC) upregulation by gram-positive and gram-negative bacteria. Biochem. Biophys. Acta 1406 (1998) 251-259
15. Smirnova M.G., Kiselev S.L., Birchall J.P., and Pearson J.P. Up-regulation of mucin secretion in HT29-MTX cells by the pro-inflammatory cytokines tumor necrosis factor-alpha and interleukin-6. Eur. Cytokine Netw. 12 (2001) 119-125
16. Zen Y., Harada K., Sasaki M., Tsuneyama K., Katayanagi K., Yamamoto Y., and Nakanuma Y. Lipopolysaccharide induces overexpression of MUC2 and MUC5AC in cultured biliary epithelial cells. Am. J. Pathol. 161 (2002) 1475-1484
17. Fisher B.M., Rochelle L.G., Voynow J.A., Akley N.J., and Adler K.B. Tumor necrosis factor-alpha stimulates mucin secretion and cyclic GMP production by guinea pig tracheal epithelial cells in vitro. Am. J. Respir. Cell Mol. Biol. 20 (1999) 413-422
18. Buisine M.P., Desreumaux P., Leteurtre E., Copin M.C., Colombel J.F., Porcht N.J., and Aubert P. Mucin gene expression in human embryonic and foetal intestine. Gut 49 (2001) 544-551
19. Arm H.G., Flyod T.M., Faber J.E., and Hayes J.R. Use of ligated segments of rabbit small intestine in experimental shigellosis. J. Bacteriol. 89 (1965) 803-809
20. Kita M., and Marmor M.F. Retinal adhesive force in living rabbit, cat, and monkey eyes. J. Invest. Opthalmol. Visual Sci. 33 (1992) 1879-1882
21. Reis C.A., David L., Carvalho F., Mandel U., Bolos C., Mirgorodskaya E., Clausen H., and Simoes M.S. Immunohistochemical study of the expression of MUC6 mucin and co-expression of other secreted mucins (MUC5AC and MUC2) in human gastric carcinomas. J. Histochem. Cytochem. 48 (2000) 377-388
22. Towbin H., Stahelin T., and Gordon J. Modulation of proteins from polyacrylamide gel to nitrocellulose sheets: procedure and some applications. Proc. Natl. Acad. Sci. U. S. A. 76 (1979) 4350-4354
23. Bims M.M. Molecular genetics of virulence in Shigella. Microbiol. Sci. 2 (1985) 275-278
24. Mathan M.M., and Mathan V.I. Ultrastructural pathology of the rectal mucosa in Shigella dysentery. Am. J. Pathol. 123 (1986) 25-38
25. Beachey E.A. Bacterial adherence: adhesin-receptor interactions mediating the attachment of bacteria to mucosal surfaces. J. Infect. Dis. 143 (1981) 325-345
26. RajKumar R.H., Devaraj H., and Niranjali Devaraj S. Binding of Shigella to rat and human intestinal mucin. Mol. Cell. Biochem. 178 (1998) 261-268
27. Sai Sudha P., Devaraj H., and Niranjali Devaraj S. Adherence of Shigella dysenteriae 1 to human colonic mucin. J. Curr. Microbiol. 42 (2001) 381-387
28. Li J.D., Feng W., Gallup M., Kim J.H., Gum J., Kim Y., and Basbaum C. Activation of NF-kappa B via a Src-dependent Ras-MAPK-pp90rsk pathway is required for Pseudomonas aeruginosa-induced mucin overproduction in epithelial cells. Proc. Natl. Acad. Sci. U. S. A. 95 (1998) 5718-5723
29. Jung H.C., Eckmann L., Yang S., Panja A., Fierer J., Morzycka-Wroblewska E., and Kagnoff M.F. A distinct array of proinflammatory cytokines is expressed in human colon epithelial cells in response to bacterial invasion. J. Clin. Invest. 95 (1995) 55-65
30. Raqib R.B., Wretlind J., Andersson A., and Lindberg A. Cytokine secretion in acute shigellosis is correlated to disease activity and directed more to stool than to plasma. J. Infect. Dis. 171 (1995) 376-384
31. Hong D.H., Petrovics G., Anderson W.B., Forstner J., and Forstner G. Induction of mucin gene expression in human colonic cell lines by PMA is dependent on PKC-epsilon. Am. J. Physiol. 277 (1999) G1041-G1047