Neutrophils as one of the major haptoglobin sources in mastitis affected milk

Veterinary Research

Volumn 40, Issue 3, 2009, Pages

  Lai, I Hsiang ^a   Tsao, Jung Hsu ^b   Lu, Yi Ping ^c   Lee, Jai Wei ^d   Zhao, Xin ^e   Chien, Feng Lin ^a   Mao, Simon J T ^a,f  

^a NATIONAL CHIAO TUNG UNIVERSITY   (Taiwan)

^b Yong Rong Dairy Farm ^*  (Taiwan)

^c Pingtung Hsien Livestock Disease Control Center   (Taiwan)

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

^e MCGILL UNIVERSITY   (Canada)

^f ASIA UNIVERSITY   (Taiwan)

Author keywords

Haptoglobin; Immunocytochemistry; MAC T cells; Mastitis; Neutrophil

Indexed keywords

HAPTOGLOBIN; MESSENGER RNA;

ANIMAL CELL; ARTICLE; CELL CULTURE; CELL LEVEL; CONFOCAL MICROSCOPY; CONTROLLED STUDY; DAIRY CATTLE; ENZYME LINKED IMMUNOSORBENT ASSAY; FOOD CONTAMINATION; IMMUNOFLUORESCENCE TEST; IMMUNOHISTOCHEMISTRY; MASTITIS; MILK; NEUTROPHIL COUNT; NONHUMAN; POLYACRYLAMIDE GEL ELECTROPHORESIS; PROTEIN EXPRESSION; PROTEIN FOLDING; PROTEIN ISOLATION; PROTEIN PURIFICATION; PROTEIN SYNTHESIS; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SOMATIC CELL; WESTERN BLOTTING; ANIMAL; CATTLE; CATTLE DISEASE; CHEMISTRY; CYTOLOGY; FEMALE; GENE EXPRESSION REGULATION; GENETICS; METABOLISM; NEUTROPHIL; PHYSIOLOGY; UDDER;

BOVINAE;

ANIMALS; CATTLE; FEMALE; GENE EXPRESSION REGULATION; HAPTOGLOBINS; MAMMARY GLANDS, ANIMAL; MASTITIS, BOVINE; MILK; NEUTROPHILS; RNA, MESSENGER;

EID: 63849088876     PISSN: 09284249     EISSN: 12979716     Source Type: Journal    
DOI: 10.1051/vetres:2008055     Document Type: Article

References (32)

1. Boulanger V., Zhao X., Lacasse P., Protective effect of melatonin and catalase in bovine neutrophilinduced model of mammary cell damage, J. Dairy Sci. (2002) 85:562-569.
2. Chen W.L., Hwang M.T., Liau C.Y., Ho J.C., Hong K.C., Mao S.J.T., β-Lactoglobulin is a thermal marker in processed milk as studied by electrophoresis and circular dichroic spectra, J. Dairy Sci. (2005) 88:1618-1630.
3. Chen W.L., Liu W.T., Yang M.C., Hwang M.T., Tsao J.H., Mao S.J.T., A novel conformationdependent monoclonal antibody specific to the native structure of β-lactoglobulin and its application, J. Dairy Sci. (2006) 89:912-921.
4. Cooray R., Waller K.P., Venge P., Haptoglobin comprises about 10% of granule protein extracted from bovine granulocytes isolated from healthy cattle, Vet. Immunol. Immunopathol. (2007) 119:310-315.
5. Eckersall P.D., Young F.J., McComb C., Hogarth C.J., Safi S., Weber A., et al., Acute phase proteins in serum and milk from dairy cows with clinical mastitis, Vet. Rec. (2001) 148:35-41.
6. Eckersall P.D., Young F.J., Nolan A.M., Knight C.H., McComb C., Waterston M.M., et al., Acute phase proteins in bovine milk in an experimental model of Staphylococcus aureus subclinical mastitis, J. Dairy Sci. (2006) 89:1488-1501.
7. Gervois P., Kleemann R., Pilon A., Percevault F., Koenig W., Staels B., Kooistra T., Global suppression of IL-6-induced acute phase response gene expression after chronic in vivo treatment with the peroxisome proliferator-activated receptor-a activator fenofibrate, J. Biol. Chem. (2004) 279:16154-16160.
8. Grönlund U., Hallén Sandgren C., Persson Waller K., Haptoglobin and serum amyloid A in milk from dairy cows with chronic sub-clinical mastitis, Vet. Res. (2005) 36:191-198.
9. Hiss S., Mielenz M., Bruckmaier R.M., Sauerwein H., Haptoglobin concentrations in blood and milk after endotoxin challenge and quantification of mammary Hp mRNA expression, J. Dairy Sci. (2004) 87:3778-3784.
10. Huynh H.T., Robitaille G., Turner J.D., Establishment of bovine mammary epithelial cells (MAC-T): an in vitro model for bovine lactation, Exp. Cell Res. (1991) 197:191-199.
11. Kolb A.F., Engineering immunity in the mammary gland, J. Mammary Gland Biol. Neoplasia (2002) 7:123-134.
12. Kristiansen M., Graversen J.H., Jacobsen C., Sonne O., Hoffman H., Law S.K., Moestrup S.K., Identification of the haemoglobin scavenger receptor, Nature (2001) 409:198-201.
13. Lai I.H., Tsai T.I., Lin H.H., Lai W.Y., Mao S.J.T., Cloning and expression of human haptoglobin subunits in Escherichia coli: delineation of a major antioxidant domain, Protein Expr. Purif. (2007) 52:356-362.
14. Lai I.H., Lin K.Y., Larsson M., Yang M.C., Shiau C.H., Liao M.H., Mao S.J.T., A unique tetrameric structure of deer plasma haptoglobin: an evolutionary advantage in the Hp 2-2 phenotype with homogeneous structure, FEBS J. (2008) 275: 981-993.
15. Lai Y.A., Lai I.H., Tseng C.F., Lee J., Mao S.J.T., Evidence of tandem repeat and extra thiol-groups in the polymeric formation of bovine haptoglobin: a unique structure of Hp 2-2 phenotype, J. Biochem. Mol. Biol. (2007) 40:1028-1038.
16. Langlois M.R., Delanghe J.R., Biological and clinical significance of haptoglobin polymorphism in humans, Clin. Chem. (1996) 42:1589-1600.
17. Lauzon K., Zhao X., Bouetard A., Delbecchi L., Paquette B., Lacasse P., Antioxidants to prevent bovine neutrophil-induced mammary epithelial cell damage, J. Dairy Sci. (2005) 88:4295-4303.
18. Lee J.W., Zhao X., Recombinant human interleukin- 8, but not human interleukin-1beta, induces bovine neutrophil migration in an in vitro co-culture system, Cell Biol. Int. (2000) 24:889-895.
19. Merle R., Schröder A., Hamann J., Cell function in the bovine mammary gland: a preliminary study on interdependence of healthy and infected udder quarters, J. Dairy Res. (2007) 74:174-179.
20. Monks J., Neville M.C., Albumin transcytosis across the epithelium of the lactating mouse mammary gland, J. Physiol. (2004) 560:267-280.
21. Nielsen B.H., Jacobsen S., Andersen P.H., Niewold T.A., Heegaard P.M., Acute phase protein concentrations in serum and milk from healthy cows, cows with clinical mastitis and cows with extramammary inflammatory conditions, Vet. Rec. (2004) 154:361-365.
22. Olde Riekerink R.G., Barkema H.W., Veenstra W., Berg F.E., Stryhn H., Zadoks R.N., Somatic cell count during and between milkings, J. Dairy Sci. (2007) 90:3733-3741.
23. Pedersen L.H., Aalbaek B., Røntved C.M., Ingvartsen K.L., Sorensen N.S., Heegaard P.M., Jensen H.E., Early pathogenesis and inflammatory response in experimental bovine mastitis due to Streptococcus uberis, J. Comp. Pathol. (2003) 128:156-164.
24. Petersen H.H., Nielsen J.P., Heegaard P.M., Application of acute phase protein measurements in veterinary clinical chemistry, Vet. Res. (2004) 35:163-187.
25. Poutrel B., Stegemann M.R., Roy O., Pothier F., Tilt N., Payne-Johnson M., Evaluation of the efficacy of systemic danofloxacin in the treatment of induced acute Escherichia coli bovine mastitis, J. Dairy Res. (2008) 75:310-318.
26. Pyörälä S., Indicator of inflammation in the diagnosis of mastitis, Vet. Res. (2003) 34:565-578.
27. Rainard P., Riollet C., Innate immunity of the bovine mammary gland, Vet. Res. (2006) 37:369-400.
28. Theilgaard-Mönch K., Jacobsen L.C., Nielsen M.J., Rasmussen T., Udby L., Gharib M., et al., Haptoglobin is synthesized during granulocyte differentiation, stored in specific granules, and released by neutrophils in response to activation, Blood (2006) 108:353-361.
29. Thielen M.A., Mielenz M., Hiss S., Zerbe H., Petzl W., Schuberth H.J., et al., Short communication: Cellular localization of haptoglobin mRNA in the experimentally infected bovine mammary gland, J. Dairy Sci. (2007) 90:1215-1219.
30. Tseng C.F., Lin C.C., Huang H.Y., Liu H.C., Mao S.J.T., Antioxidant role of human haptoglobin, Proteomics (2004) 4:2221-2228.
31. Tseng C.F., Mao S.J.T., Analysis of antioxidant as a therapeutic agent for atherosclerosis, Curr. Pharm. Anal. (2006) 2:369-384.
32. Wagner L., Gessl A., Parzer S.B., Base W., Waldhäusl W., Pasternack M.S., Haptoglobin phenotyping by newly developed monoclonal antibodies. Demonstration of haptoglobin uptake into peripheral blood neutrophils and monocytes, J. Immunol. (1996) 156:1989-1996.