Expression of bovine granulocyte chemotactic protein-2 (GCP-2) in neutrophils and a mammary epithelial cell line (MAC-T) in response to various bacterial cell wall components

Veterinary Journal

Volumn 186, Issue 1, 2010, Pages 89-95

  Yu, Chi ^a   Shi, Zhao Ru ^a   Chu, Chun Yen ^a   Lee, Kuo Hua ^b   Zhao, Xin ^c   Lee, Jai Wei ^a  

^a NATIONAL PINGTUNG UNIVERSITY OF SCIENCE AND TECHNOLOGY   (Taiwan)

^b Hsin Chu Branch Station   (Taiwan)

^c MCGILL UNIVERSITY   (Canada)

Author keywords

Bacterial cell wall components; Bovine; Granulocyte chemotactic protein 2; Mammary epithelial cells; Mastitis; Polymorphonuclear neutrophils

Indexed keywords

BACTERIUM LIPOPOLYSACCHARIDE; GRANULOCYTE CHEMOTACTIC PROTEIN 2; INTERLEUKIN 8; LIPOTEICHOIC ACID; PEPTIDOGLYCAN;

ANIMAL CELL; ANIMAL TISSUE; ARTICLE; BACTERIAL CELL WALL; BOVINE MASTITIS; BREAST EPITHELIUM; CATTLE; CONTROLLED STUDY; ESCHERICHIA COLI; GENE EXPRESSION; LEUKOCYTE MIGRATION; NEUTROPHIL; NEUTROPHIL CHEMOTAXIS; NONHUMAN; NUCLEOTIDE SEQUENCE; STAPHYLOCOCCUS AUREUS; UPREGULATION;

ANIMALS; CATTLE; CELL LINE; CHEMOKINE CXCL6; CHEMOTACTIC FACTORS; EPITHELIAL CELLS; ESCHERICHIA COLI; FEMALE; HUMANS; INTERLEUKIN-8; LIPOPOLYSACCHARIDES; MAMMARY GLANDS, ANIMAL; MASTITIS, BOVINE; NEUTROPHILS; PEPTIDOGLYCAN; RECOMBINANT PROTEINS; TEICHOIC ACIDS;

BACTERIA (MICROORGANISMS); BOS; BOVINAE; ESCHERICHIA COLI; NEGIBACTERIA; POSIBACTERIA;

EID: 77958169555     PISSN: 10900233     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tvjl.2009.07.012     Document Type: Article

References (36)

1. Akarsu E.S., Mamuk S. Escherichia coli lipopolysaccharides produce serotype-specific hypothermic response in biotelemetered rats. American Journal of Physiology - Regulatory, Integrative and Comparative Physiology 2007, 292:R1846-R1850.
2. Bannerman D.D., Paape M.J., Lee J.-W., Zhao X., Hope J.C., Rainard P. Escherichia coli and Staphylococcus aureus elicit differential innate immune responses following intramammary infection. Clinical Diagnostic Laboratory Immunology 2004, 11:463-472.
3. Bannerman D.D., Kauf A.C., Paape M.J., Springer H.R., Goff J.P. Comparison of Holstein and Jersey innate immune responses to Escherichia coli intramammary infection. Journal of Dairy Science 2008, 91:2225-2235.
4. Burvenich C., Paape M.J., Hill A.W., Guidry A.J., Miller R.H., Heyneman R., Kremer W.D., Brand A. Role of the neutrophil leukocyte in the local and systemic reactions during experimentally induced E. coli mastitis in cows immediately after calving. Veterinary Quarterly 1994, 16:45-50.
5. Fillmore R.A., Nelson S.E., Lausch R.N., Oakes J.E. Differential regulation of ENA-78 and GCP-2 gene expression in human corneal keratinocytes and epithelial cells. Investigative Ophthalmology and Visual Science 2003, 44:3432-3437.
6. Huynh H.T., Robitaille G., Turner J.D. Establishment of bovine mammary epithelial cells (MAC-T): an in vitro model for bovine lactation. Experimental Cell Research 1991, 197:191-199.
7. Kumar A., Zhang J., Yu F.-S.X. Innate immune response of corneal epithelial cells to Staphylococcus aureus infections: role of peptidoglycan in stimulating proinflammatory cytokine secretion. Investigative Ophthalmology and Visual Science 2004, 45:3513-3522.
8. Lahouassa H., Moussay E., Rainard P., Riollet C. Differential cytokine and chemokine responses of bovine mammary epithelial cells to Staphylococcus aureus and Escherichia coli. Cytokine 2007, 38:12-21.
9. Lee J.-W., Zhao X. Recombinant human interleukin-8, but not human interleukin-1β, induces bovine neutrophil migration in an in vitro co-culture system. Cell Biology International 2000, 24:889-895.
10. Lee, J.-W., Huang, M.-K., Roy, M., Zhao, X., 2005. Identification of novel genes expressed in bovine mammary epithelial cells in response to Staphylococcus aureus cell wall components by differential display. In: Proceedings of the 4th International Dairy Federation International Mastitis Conference, Maastricht, The Netherlands, 12-15 June 2005.
11. Lee J.-W., Bannerman D.D., Paape M.J., Huang M.-K., Zhao X. Characterization of cytokine expression in milk somatic cells during intramammary infections with Escherichia coli or Staphylococcus aureus by real-time PCR. Veterinary Research 2006, 37:219-229.
12. Lin Y., Xia L., Turner J.D., Zhao X. Morphologic observation of neutrophil diapedesis across bovine mammary gland epithelium in vitro. American Journal of Veterinary Research 1995, 56:203-207.
13. Lin Y., Cai J., Turner J.D., Zhao X. Quantification of bovine neutrophil migration across mammary epithelium in vitro. Canadian Journal of Veterinary Research 1996, 60:145-149.
14. McClenahen D., Krueger R., Lee H.-Y., Thomas C., Kehrli M.E., Czuprynski C. Interleukin-8 expression by mammary gland endothelial and epithelial cells following experimental mastitis infection with E. coli. Comparative Immunology Microbiology and Infectious Diseases 2006, 29:127-137.
15. Melmed G., Thomas L.S., Lee N., Tesfay S.Y., Lukasek K., Michelsen K.S., Zhou Y., Hu B., Arditi M., Abreu M.T. Human intestinal epithelial cells are broadly unresponsive to toll-like receptor 2-dependent bacterial ligands: implications for host-microbial interactions in the gut. Journal of Immunology 2003, 170:1406-1415.
16. Morath S., Geyer A., Hartung T. Structure-function relationship of cytokine induction by lipoteichoic acid from Staphylococcus aureus. Journal of Experimental Biology 2001, 193:393-397.
17. Morath S., Geyer A., Spreitzer I., Hermann C., Hartung T. Structural decomposition and heterogeneity of commercial lipoteichoic acid preparations. Infection and Immunity 2002, 70:938-944.
18. Morsey M.A., Popowych J., Kowalski J., Gerlach G., Godson D., Campos M., Babiuk L.A. Molecular cloning and expression of bovine interleukin-8. Microbial Pathogenesis 1996, 20:203-212.
19. Paape M.J., Wergin W.P., Guidry A.J., Pearson R.E. Leukocytes-second line of defense against invading mastitis pathogens. Journal of Dairy Science 1979, 62:135-153.
20. Petzl W., Zerbe H., Günther J., Yang W., Seyfert H.-M., Nürnberg G., Schuberth H.-J. Escherichia coli, but not Staphylococcus aureus triggers an early increased expression of factors contributing to innate immune defense in the udder of the cow. Veterinary Research 2008, 39:18.
21. Proost P., De Wolf-Peeters C., Conings R., Opdenakker G., Billiau A., Van Damme J. Identification of a novel granulocyte chemotactic protein (GCP-2) from human tumor cells: in vitro and in vivo comparison with natural forms of GRO, IP-10, and IL-8. Journal of Immunology 1993, 150:1000-1010.
22. Proost P., Wuytes A., Conings R., Lenaerts J.P., Billiau A., Opdenakker G., Van Damme J. Human and bovine granulocyte chemotactic protein-2: complete amino acid sequence and functional characterization as chemokines. Biochemistry 1993, 32:10170-10177.
23. Rainard P., Fromageau A., Cunha P., Gilbert F.B. Staphylococcus aureus lipoteichoic acid triggers inflammation in the lactating bovine mammary gland. Veterinary Research 2008, 39:52.
24. Sachse F., Ahlers F., Stoll W., Redack C. Neutrophil chemokines in epithelial inflammatory processes of human tonsils. Clinical and Experimental Immunology 2005, 140:293-300.
25. SAS/STAT User's Guide, 2000. Version 8, SAS Institution Inc., Cary, NC.
26. Seiler P., Aichele P., Raupach B., Odermatt B., Steinhoff U., Kaufmann H.E. Rapid neutrophil response controls fast-replicating intracellular bacteria but not slow-replicating Mycobacterium tuberculosis. Journal of Infectious Diseases 2000, 181:671-680.
27. Sheehy R.A., Della-Vedova J.J., Nicholas K.R., Wynn P.C. Hormone-dependent milk protein gene expression in bovine mammary explants from biopsies at different stages of pregnancy. Journal of Dairy Research 2004, 71:135-140.
28. Strandberg Y., Gray C., Vuocolo T., Donaldson L., Broadway M., Tellam R. Lipopolysaccharide and lipoteichoic acid induce different innate immune responses in bovine mammary epithelial cells. Cytokine 2005, 31:72-86.
29. Strieter R.M., Polverini P.J., Kunkel S.L., Arenberg D.A., Burdick M.D., Kasper J., Dzuiba J., Van Damme J., Walz A., Marriott D. The functional role of the ELR motif in CXC chemokine-mediated angiogenesis. Journal of Biological Chemistry 1995, 270:27348-27357.
30. Swanson K.M., Dobson K., Henderson D.H.V., Davis S.R., Farr V.C., Singh K. Transcriptome profiling of Streptococcus uberis induced mastitis reveals fundamental differences between immune gene expression in the mammary gland and in a primary cell culture model. Journal of Dairy Science 2009, 93:117-129.
31. 2-terminal sequence-characterized human monokine possessing neutrophil chemotactic, skin-reactive, and granulocytosis-promoting activity. Journal of Experimental Medicine 1988, 167:1364-1376.
32. Van Damme J., Wuyts A., Froyen G., Van Coillie E., Struyf S., Billiau A., Proost P., Wang J.M., Opdenakker G. Granulocyte chemotactic protein-2 and related CXC chemokines: from gene regulation to receptor usage. Journal of Leukocyte Biology 1997, 62:563-569.
33. Vandercappellen J., Van Damme J., Struyl S. The role of CXC chemokines and their receptors in cancer. Cancer Letters 2008, 267:226-244.
34. Wolf M., Delgado M.B., Jones S.A., Dewald B., Clark-Lewis I., Baggiolini M. Granulocyte chemotactic protein 2 acts via both IL-8 receptors, CXCR1 and CXCR2. European Journal of Immunology 1998, 28:164-170.
35. Wuyts A., Haelens A., Proost P., Lenaerts J.-P., Conings R., Opdenakker G., Van Damme J. Identification of mouse granulocyte chemotactic protein-2 from fibroblasts and epithelial cells. Functional comparison with natural KC and macrophage inflammatory protein-2. Journal of Immunology 1996, 157:1736-1743.
36. Wuyts A., Struyf S., Gijsbers K., Schutyser E., Put W., Conings R., Lenaerts J.-P., Geboes K., Opdenakker G., Menten P., Proost P., Van Damme J. The CXC chemokine GCP-2/CXCL6 is predominantly induced in mesenchymal cells by interleikin-1β and is down-regulated by interferon-γ: comparison with interleukin-8/CXCL8. Laboratory Investigation 2003, 83:23-33.