Effect of fetal bovine serum and heat-inactivated fetal bovine serum on microbial cell wall-induced expression of procoagulant activity by equine and canine mononuclear cells in vitro

American Journal of Veterinary Research

Volumn 67, Issue 6, 2006, Pages 1020-1024

  Okano, Shozo ^a,b   Hurley, David J ^b   Vandenplas, Michel L ^b   Moore, James N ^b  

^a KITASATO UNIVERSITY   (Japan)

^b UNIVERSITY OF GEORGIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

LIPOPOLYSACCHARIDE; LIPOPOLYSACCHARIDE BINDING PROTEIN; MONOCLONAL ANTIBODY; POLYMYXIN B; PROCOAGULANT; RECOMBINANT PROTEIN; ZYMOSAN;

ANIMAL CELL; ARTICLE; BACTERIAL CELL WALL; CELL ISOLATION; CELL STIMULATION; CONTAMINATION; CONTROLLED STUDY; CULTURE MEDIUM; DOG; FEMALE; HEAT TREATMENT; HORSE; IN VITRO STUDY; MALE; MONONUCLEAR CELL; NONHUMAN; SENSITIVITY ANALYSIS; SERUM; YEAST CELL;

ANIMALS; BLOOD COAGULATION FACTORS; CATTLE; CELL WALL; DOGS; DOSE-RESPONSE RELATIONSHIP, DRUG; FEMALE; GENE EXPRESSION REGULATION; HORSES; HUMANS; LEUKOCYTES, MONONUCLEAR; LIPOPOLYSACCHARIDES; MALE; ZYMOSAN;

BACTERIA (MICROORGANISMS); BOS TAURUS; CANIS FAMILIARIS; EQUIDAE;

EID: 33745665011     PISSN: 00029645     EISSN: None     Source Type: Journal    
DOI: 10.2460/ajvr.67.6.1020     Document Type: Article

References (26)

1. Camerer E, Kolsto AB, Prydz H. Cell biology of tissue factor, the principal initiator of blood coagulation. Thromb Res 1996;81:1-41
2. Grunig G, Winder C, Hulliger C, et al. Expression of pro-coagulant activity by equine lung macrophages: stimulation by blood lymphocytes Res Vet Sci 1991;51:278-284
3. Henry MM, Moore JN. Endotoxin-induced procoagulant activity in equine peripheral blood monocytes. Circ Shock 1988;26:297-309
4. Ouellette AL, Evans RJ, Heath MF. Platelets enhance endotoxin-induced monocytes tissue factor (TF) activity in the horse. Res Vet Sci 2004;76:31-35.
5. Heumann D, Gallay P, Barras C, et al. Control of LPS binding and LPS-induced TNF secretion in human peripheral blood monocytes. J Immunol 1992; 148:3505-3512
6. Steinemann S, Ulevitch RJ, Mackman N. Role of the lipopolysaccharide (LPS)-binding protein/CD14 pathway in LPS induction of tissue factor expression in monocytic cells. Arterioscler Thromb 1994;14:1202-1209.
7. Yang Z, Khemlani LS, Dean DF, et al. Serum components enhance bacterial lipopolysaccharide-induced tissue factor expression and tumor necrosis factor-α secretion by bovine alveolar macrophages in vitro. J Leukoc Biol 1994;55:483-488
8. Chu AJ, Moore J, Sampsell RN. Daily supplementation with MaxEPA suppresses endotoxin-inducible monocytic procoagulation in dogs. J Surg Res 1997;71:93-99
9. Vickers J, Russwurm S, Dohrn B, et al Monocyte tissue factor (CD142) and Mac-1 (CD11b) are increased in septic patients. Thromb Haemost 1998;79:1219-1222.
10. Osterud B, Bjorklid E. The tissue factor pathway in disseminated intravascular coagulation. Semin Thromb Haemost 2001;27:605-617.
11. Beutler B, Hoebe K, Du X, et al. How we detect microbes and respond to them: the Toll-like receptors and their transducers. J Leukoc Biol 2003;74:479-485.
12. Henry MM, Moore JN. Clinical relevance of monocytes pro-coagulant activity in horses with colic. J Am Vet Med Assoc 1991;198:843-848.
13. Barton MH, Collatos C, Moore JN. Endotoxin induced expression of tumour necrosis factor, tissue factor and plasminogen activator inhibitor activity by peritoneal macrophages. Equine Vet J 1996;28:382-389
14. Adam R, Kuczera F, Kohler H, et al. Superoxide anion generation in human milk macrophages: opsonin-dependent versus opsonin-independent stimulation compared with blood monocytes Pediatr Res 2001;49:435-439
15. Miyake K. Innate recognition of lipopolysaccharide by Toll-like receptor 4-MD-2. Trends Microbiol 2004;12:186-192.
16. Schumann RR, Leong SR, Flaggs GW, et al. Structure and function of lipopolysaccharide binding protein Science 1990; 249:1429-1431.
17. Van Amersfoot ES, Van Berkel TJC, Kuiper J. Receptors, mediators, and mechanisms involved in bacterial sepsis and septic shock. Clin Microbiol Rev 2003;16:379-414
18. Boone CE, Mantel N, Caruso TD, et al. Quality control studies on fetal bovine serum used in tissue culture. In Vitro 1972;7:174-189
19. Pinyopummintr T, Bavister BD. Development of bovine embryos in a cell-free medium: effects of type of serum, timing of its inclusion and heat inactivation. Theriogenology 1994; 41:1241-1249
20. Carneiro LAM, Travassos LH, Philpott DJ. Innate immune recognition of microbes through Nod1 and Nod2: implications for disease. Microbes Infect 2004;6:609-616.
21. Beutler B. Not "molecular patterns" but molecules. Immunity 2005;19:155-158
22. Evans SE, Hahn PY, McCann F, et al Pneumocystis cell wall beta-glucans stimulate alveolar epithelial cell chemokine generation through nuclear factor-ΚB-dependent mechanisms Am J Respir Cell Mol Biol 2005; 32:490-497
23. Landmann R, Muller B, Zimmerli W. CD14, new aspects of ligand and signal diversity. Microbes Infect 2000;2:295-304.
24. Webber JR, Freyer D, Alexander C, et al Recognition of pneumonococcal peptidoglycan: an expanded, pivotal role for LPS binding protein. Immunity 2003;19:269-279
25. Murray PJ. NOD proteins: an intracellular pathogen-recognition system or signal transduction modifiers? Curr Opin Immunol 2005;17:352-358.
26. Grondahl G, Johannisson A, Jensen-Waern M, et al. Opsonization of yeast cells with equine iC3b, C3b and IgG. Vet Immunol Immunopathol 2001;80:209-223.