Vet Med - Czech, 2008, 53(1):1-11 | DOI: 10.17221/1935-VETMED

Expression of CD14 and CD44 on bovine polymorphonuclear leukocytes during resolution of mammary inflammatory response induced by muramyldipeptide and lipopolysaccharide

T. Langrova1,2, Z. Sladek1,2, D. Rysanek2
1 Mendel University of Agriculture and Forestry, Brno, Czech Republic
2 Veterinary Research Institute, Brno, Czech Republic

The aim of the study was to prove the effect of muramyldipeptide and lipopolysaccharide on the expression of CD14 and CD44 during an induced inflammatory response of the mammary gland and its resolution. The purpose was to clarify whether the CD14 and CD44 expression is controlled by the mechanisms of resolution. The CD44 had previously been judged to be an activation marker along with CD11b on polymorphonuclear leukocytes. The experimental inflammatory response was induced by muramyldipeptide and lipopolysaccharide, while phosphate buffered saline was used as a control. The course of the inflammatory response was monitored at four time points: 24 h and 48 h (initiation of inflammatory response), 72 h and 168 h (resolution of inflammatory response). The total number of cells was determined by a hemocytometer. Flow cytometry was used to determine differential counts of leukocytes, proportions of CD11b+ polymorphonuclear leukocytes, proportions of apoptotic and necrotic polymorphonuclear leukocytes, and proportions of CD14+ and CD44+ polymorphonuclear leukocytes. The proportion of CD11b+ polymorphonuclear leukocytes after induction of inflammation with muramyldipeptide was higher (P < 0.05) compared to that after induction by phosphate buffered saline, was highly significantly greater after lipopolysaccharide (P < 0.01), and remained at approximately the same level for the whole period of observation (168 h). A higher proportion of CD14+ polymorphonuclear leukocytes was observed 72 h after induction with phosphate buffered saline. A statistically highly significant lower proportion was observed after induction with muramyldipeptide (P < 0.01), and a statistically significant lower proportion was observed after induction with lipopolysaccharide (P < 0.05). Decrease in the proportion of CD14+ polymorphonuclear leukocytes followed. In the initial phase of the inflammatory response (24 to 72 h) there was a gradual increase in the proportion of CD44+ polymorphonuclear leukocytes, and more so after the phosphate buffered saline. A greatly lower proportion of CD44+ polymorphonuclear leukocytes was observed after administration of muramyldipeptide and lipopolysaccharide: 24 h (P < 0.01), 48 h (P < 0.05) and 72 h (P < 0.01). Compared with muramyldipeptide and lipopolysaccharide, there was a statistically highly significant (P < 0.01) lower proportion of CD44+ polymorphonuclear leukocytes observed 168 h after induction with phosphate buffered saline. Hence the proportion of CD44+ polymorphonuclear leukocytes is low in the initial phase of inflammation, and CD44, in contrast with CD11b, does not appear to be a polymorphonuclear marker of activation. The results of the study have shown that expression of CD14 and CD44 is controlled by the factors inducing inflammatory response as well as by the mechanisms of resolution.

Keywords: heifer; mammary gland; inflammation; bacterial toxins; apoptosis

Published: January 31, 2008  Show citation

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Langrova T, Sladek Z, Rysanek D. Expression of CD14 and CD44 on bovine polymorphonuclear leukocytes during resolution of mammary inflammatory response induced by muramyldipeptide and lipopolysaccharide. Vet Med - Czech. 2008;53(1):1-11. doi: 10.17221/1935-VETMED.
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References

  1. Akgul C., Moulding D.A., Edwards S.W. (2001): Molecular control of neutrophil apoptosis. FEBS Letters, 487, 318-322. Go to original source... Go to PubMed...
  2. Bannerman D.D., Paape M.J., Lee J.W., Zhao X., Hope J.C., Rainard P. (2004): Escherichia coli and Staphylococcus aureus elicit differential innate immune re sponses following intramammary infection. Clinical and Diagnostic Laboratory Immunology, 11, 463- 472. Go to original source... Go to PubMed...
  3. Capuco A.V., Paape M.J., Nickerson S.C. (1986): In vitro study of polymorphonuclear leukocyte damage to mammary tissues of lactating cows. American Journal of Veterinary Research, 47, 663-668.
  4. Dosogne H., Vangroenweghe F., Mehrzad J., MassartLeen A.M., Burvenich C. (2003): Differential leukocyte count method for bovine low somatic cell count milk. Journal of Dairy Science, 86, 828-834. Go to original source... Go to PubMed...
  5. Fenton M.J., Golenbock D.T. (1998): LPS-binding proteins and receptors. Journal of Leukocyte Biology, 64, 25-32. Go to original source... Go to PubMed...
  6. Gregory C.D., Devitt A. (1999): CD14 and apoptosis. Apoptosis, 4, 11-20. Go to original source... Go to PubMed...
  7. Heidenreich S. (1999): Monocyte CD14: a multifunctional receptor engaged in apoptosis from both sides. Journal of Leukocyte Biology, 65, 737-743. Go to original source... Go to PubMed...
  8. Hughes J.R., Johnson A., Mooney C., Hugo K., Gordon J., Savill J. (1997): Neutrophil fate in experimental glomerular capillary injury in the rat. American Journal of Pathology, 150, 223-234.
  9. Khan A.I., Kerfoot S.M., Heit B., Liu L., Andonegui G., Ruffell B., Johnson P., Kubes P. (2004): Role of CD44 and hyaluronan in neutrophil recruitment. The Journal of Immunology, 173, 7594-7601. Go to original source... Go to PubMed...
  10. Liu J.J., Song C.W., Yue Y., Duan C.G., Yang J., He T., He Y.Z. (2005): Quercetin inhibits LPS-induced delay in spontaneous apoptosis and activation of neutrophils. Inflammation Research, 54, 500-507. Go to original source... Go to PubMed...
  11. Maliszewski C.R. (1991): CD14 and immune response to lipopolysaccharide. Science, 252, 1321-1322. Go to original source... Go to PubMed...
  12. Matouskova O., Cigler M., Chalupa K., Hruska K. (1992): STAT Plus - Manual (in Czech). 1st ed. Veterinary Research Institute, Brno. 168 pp.
  13. Meagher L.C., Savill J., Baker A., Fuller R.W., Haslett C.H. (1992): Phagocytosis of apoptotic neutrophils does not induce macrophage release of thromboxan B2. Journal of Leukocyte Biology, 52, 269-273. Go to original source... Go to PubMed...
  14. Messmer U.K., Pfeilschifter J. (2000): New insights into the mechanism for clearance of apoptotic cells. Bioassays, 22, 878-881. Go to original source... Go to PubMed...
  15. Otterlei M., Sundan A., Skjak-Braek G., Ryan L., Smidsrod O., Espevik T. (1993): Similar mechanisms of action of defined polysaccharides and lipopolysaccharides: characterization of binding and tumor necrosis factor-α induction. Infection and Immunity, 61, 1917-1925. Go to original source... Go to PubMed...
  16. Paape M.J., Lilius E.M., Wiitanen P.A., Kontio M.P., Miller R.H. (1996): Intramammary defense against infections induced by Escherichia coli in cows. American Journal of Veterinary Research, 57, 477-482. Go to original source...
  17. Paape M.J., Bannerman D.D., Zhao X., Lee J. (2003): The bovine neutrophil: Structure and function in blood and milk. Veterinary Research, 34, 597-627. Go to original source... Go to PubMed...
  18. Rambeaud M., Almeida R.A., Pighetti G.M., Oliver S.P. (2003): Dynamics of leukocytes and cytokines during experimentally induced Streptococcus uberis mastitis. Veterinary Immunology and Immunopathology, 96, 193-205. Go to original source... Go to PubMed...
  19. Rysanek D., Sladek Z., (2006): The image of exocytosis during neutrophils and macrophages phagocytic activities in inflammation of mammary gland triggered by experimental Staphylococcus aureus infection. Anatomia Histologia Embryologia, 35, 171-177. Go to original source... Go to PubMed...
  20. Rysanek D., Babak V., Sladek Z., Toman M. (2001): Variations among unbred heifers in the activities of polymorphonuclear leukocytes from the mammary gland and blood. Journal of Veterinary Medicine, Series B, 48, 31-41. Go to original source...
  21. Rysanek D., Sladek Z., Vasickova D., Faldyna M.: (2005): Effects of certain inducers of leukocytes migration into the bovine mammary gland on neutrophil apoptosis manifestation in a subsequent in vitro cultivation. Physiological Research, 54, 305-312. Go to original source...
  22. Rysanek D., Sladek Z., Babak V., Vasickova D., Hubackova M. (2006): Spontaneous and induced cytolysis of leukocytes from bovine mammary gland in the course of cultivation in vitro - the correlation with neutrophil granulocytes apoptosis. Veterinarni Medicina, 51, 265-277. Go to original source...
  23. Savill J.S. (1997): Recognition and phagocytosis of cell undergoing apoptosis. British Medical Bulletin, 53, 491-508. Go to original source... Go to PubMed...
  24. Savill J.S., Fadok V., Henson P., Haslett C. (1993): Phagocyte recognition of cells undergoing apoptosis. Immunology Today, 14, 131-136. Go to original source... Go to PubMed...
  25. Savill J.S., Gregory C., Haslett C. (2003): Cell biology. Eat me or die. Science, 302, 1516-1517. Go to original source... Go to PubMed...
  26. Schutt Ch. (1999): Molecules in focus, CD14. The International Journal of Biochemistry and Cell Biology, 31, 545-549. Go to original source... Go to PubMed...
  27. Sladek Z., Rysanek D. (2000): Apoptosis of polymorphonuclear leukocytes of the juvenile bovine mammary gland during induced influx. Veterinary Research, 31, 553-563. Go to original source... Go to PubMed...
  28. Sladek Z., Rysanek D. (2001): Neutrophil apoptosis during the resolution of bovine mammary gland injury. Research in Veterinary Science, 70, 41-46. Go to original source... Go to PubMed...
  29. Sladek Z., Rysanek D. (2006): The role of CD14 during resolution of experimentally induced Staphylococcus aureus and Streptococcus uberis mastitis. Comparative Immunology, Microbiology and Infectious Diseases, 29, 243-262. Go to original source... Go to PubMed...
  30. Sladek Z., Rysanek D., Faldyna M. (2001a): Light microscopic and flow cytometric detection of apoptosis and necrosis of neutrophils in the mammary gland of the virgin heifer. Acta Veterinaria Brno, 70, 149-155. Go to original source...
  31. Sladek Z., Rysanek D., Faldyna M. (2001b): Leukocytes in bovine virgin mammary gland: flow cytometry imaging during development and resolution of induced influx. Veterinarni Medicina, 46, 190-198. Go to original source...
  32. Sladek Z., Rysanek D., Faldyna M. (2002): Activation of phagocytes during initiation and resolution of mammary gland injury induced by lipopolysaccharide in heifers. Veterinary Research, 33, 191-204. Go to original source... Go to PubMed...
  33. Sladek Z., Rysanek D., Ryznarova H., Faldyna M. (2005): Neutrophil apoptosis during experimentally induced Staphylococcus aureus mastitis. Veterinary Research, 36, 629-643. Go to original source... Go to PubMed...
  34. Smith G.S. (2000): Neutrophils. In: Feldman B.F., Zinkl J.G, Jain N.C. (eds.): Schalm´s Veterinary Hematology. Lippincott Williams and Wilkins, Philadelphia. 281- 296.
  35. Takeuchi O., Hoshino K., Kawai T., Sanjo H., Takada H., Ogawa T., Takada K., Akira S. (1999): Differential roles of TLR2 and TLR4 in recognition of Gram-negative and Gram-positive bacterial cell wall components. Immunity, 11, 443-451. Go to original source... Go to PubMed...
  36. Takeuchi O., Hoshino K., Akira S. (2000a): Cutting edge: TLR2-deficient and MyD88-deficient mice are highly susceptible to Staphylococcus aureus infection. Journal of Immunology, 165, 5392-5396. Go to original source... Go to PubMed...
  37. Takeuchi O., Takeda K., Hoshino K., Adachi O., Ogawa T., Akira S. (2000b): Cellular responses to bacterial cell wall components are mediated through MyD88dependent signaling cascades. International Immunology, 12, 113-117. Go to original source... Go to PubMed...
  38. Teder P., Vandivier R.W., Jiang D., Liang J., Cohn L., Pure E., Henson P.M., Noble P.W. (2002): Resolution of lung inflammation by CD44. Science, 296(5565), 155-158. Go to original source... Go to PubMed...
  39. Trotter J. (2000): WinMDI 2.8 software. Windows Multiple Document Interface Flow Cytometry Application.
  40. Vachon E., Martin R., Plumb J., Kwok V., Vandivier R. W., Glogauer M., Kapus A., Wang X., Chow C.W., Grinstein S., Downey G.P. (2006): CD44 is a phagocytic receptor. Blood, 107, 4149-4158. Go to original source... Go to PubMed...
  41. Van Miert A.S. (1991): Acute phase response and non cellular defense mechanisms. Flemish Veterinary Journal, 62, 69-91. Go to PubMed...
  42. Van Oostveldt K., Paape M.J., Dosogne H., Burvenich C. (2002): Effect of apoptosis on phagocytosis, respiratory burst and CD18 adhesion receptor expression of bovine neutrophils. Domestic Animal Endocrinology, 22, 37-50. Go to original source... Go to PubMed...
  43. Vermes I., Haanen C., Steffens-Nakken H., Reutellingsperger C. (1995): A novel assay for apoptosis. Flow cytometric detection of phosphatidylserine expression on early apoptotic cells using fluorescein labelled Annexin V. Journal of Immunological Methods, 184, 39-51. Go to original source... Go to PubMed...
  44. Vivers S., Dransfield I., Hart S.P. (2002): Role of macrophage CD44 in the disposal of inflammatory cell corpses. Clinical Science, 103, 441-449. Go to original source... Go to PubMed...

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