Flow cytometric analysis of crayfish haemocytes activated by lipopolysaccharides

Fish and Shellfish Immunology

Volumn 17, Issue 3, 2004, Pages 223-233

  Cárdenas, Washington ^a   Dankert, John R ^a   Jenkins, Jill A ^b  

^a UNIVERSITY OF LOUISIANA AT LAFAYETTE   (United States)

^b NATIONAL WETLANDS RESEARCH CENTER   (United States)

Author keywords

Crayfish; Flow cytometry; Haemocyte; Innate immunity; Lipopolysaccharide

Indexed keywords

ASTACOIDEA; BACTERIA (MICROORGANISMS); INVERTEBRATA; MAMMALIA; NEGIBACTERIA; PROCAMBARUS; SALMONELLA; SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR MINNESOTA;

EID: 3342960004     PISSN: 10504648     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.fsi.2003.03.001     Document Type: Article

References (44)

1. Schletter J., Heine H., Ulmer A., Rietschel E. Molecular mechanisms of endotoxin activity. Arch Microbiol. 164:1995;383-389
2. Bayston K., Cohen J. Bacterial endotoxin and current concepts in the diagnosis and treatments of endotoxaemia. J Exp Med. 31:1990;73-83
3. Nakano M., Shinomiya H. The Lps mutational defect in C3H/HeJ mice. Morrison D.C., Ryan J.L. Bacterial endotoxic lipopolysaccharides: molecular biochemistry and cellular biology. Bacterial endotoxic lipopolysaccharides: molecular biochemistry and cellular biology. vol. I:1999;311-328 CRC Press, Boca Raton, FL
4. Gessani S., Testa U., Varano B., Marzio P., Borghi P., Conti L., et al. Enhanced production of LPS-induced cytokines during differentiation of human monocytes to macrophages. J Immunol. 151:1993;3758-3766
5. Raetz C. Bacterial lipopolysaccharides: a remarkable family of bioactive macroamphiphiles. Neidhardt F.C., Curtiss R. Escherichia coli and Salmonella: cellular and molecular biology. 1996;1035-1063 ASM Press, Washington, DC
6. Janeway C.A. Jr., Medzhitov R. Innate immune recognition. Annu Rev Immunol. 20:2002;197-216
7. Wright S. Toll, a new piece in the puzzle of innate immunity. J Exp Med. 189:1999;605-609
8. Kawai T., Takeuchi O., Fujita T., Inoue J.-I., Mühlradt P.F., Sato S., et al. Lipopolysaccharide stimulates the MyD88-independent pathway and results in activation of IFN-regulatory factor 3 and the expression of a subset of lipopolysaccharide-inducible genes. J Immunol. 167:2001;5887-5894
9. Iwanaga S., Kawabata S., Miura Y., Seki N., Shigenaga T., Muta T. Clotting cascade in the immune response of horseshoe crab. Hoffmann J.A., Janeway C.A.J., Natori S. Phylogenetic perspective in immunity: the insect host defense. 1994;79-96 Landes, London
10. Lorenzon S., Guarrini S.D., Smith V., Ferrero E. Effects of LPS injection on circulating haemocytes in crustaceans in vivo. Fish Shellfish Immunol. 9:1999;31-50
11. Söderhäll K., Cerenius L., Johansson M.W. The prophenoloxidase activating system and its role in invertebrate defence. Ann N Y Acad Sci. 712:1994;155-161
12. Cárdenas W., Dankert J.R. Phenoloxidase specific activity in the red swamp crayfish Procambarus clarkii. Fish Shellfish Immunol. 7:1997;283-295
13. Söderhäll K., Häll L. Lipopolysaccharide-induced activation of prophenoloxidase activating system in crayfish haemocyte lysate. Biochim Biophys Acta. 797:1984;99-104
14. Lee S.Y., Wang R., Söderhäll K. A lipopolysaccharide- and beta-1,3-glucan-binding protein from hemocytes of the freshwater crayfish Pacifastacus leniusculus. Purification, characterization, and cDNA cloning. J Biol Chem. 275:2000;1337-1343
15. Roux M.M., Pain A., Klimpel K.R., Dhar A.K. The lipopolysaccharide and beta-1,3-glucan binding protein gene is upregulated in white spot virus-infected shrimp (Penaeus stylirostris). J Virol. 76:2002;7140-7149
16. Johansson M.W., Söderhäll K. Exocytosis of the prophenoloxidase activating system from crayfish haemocytes. J Comp Physiol B. 156:1985;175-181
17. Cárdenas W., Jenkins J.A., Dankert J.R. A flow cytometric approach to the study of crustacean cellular immunity. J Invertebr Pathol. 76:2000;112-119
18. Renault T., Xue Q., Chilmonczyk S. Flow cytometric analysis of European flay oyster, Ostrea edulis, haemocytes using a monoclonal antibody specific for granulocytes. Fish Shellfish Immunol. 11:2001;269-274
19. Smith V.J., Söderhäll K. Induction of degranulation and lysis of haemocytes in the freshwater crayfish, Astacus astacus by components of the prophenoloxidase activating system in vitro. Cell Tissue Res. 233:1983;295-303
20. Smith V.J., Söderhäll K. β-1,3 glucan activation of crustacean hemocytes in vitro and in vivo. Biol Bull. 164:1983;299-314
21. SAS Institute Inc. SAS/STAT User's guide, Version 6. 4th ed. :1990;SAS, Cary, NC
22. Shapiro H. Shapiro H. Practical flow cytometry. 1995;Wiley-Liss, New York. p. 542
23. North R. The concept of the activated macrophage. J Immunol. 121:1978;806-809
24. Allam B., Ashton-Alcox K.A., Ford S.E. Flow cytometric measurement of hemocyte viability and phagocytic activity in the clam, Ruditapes philippinarum. J Shellfish Res. 21:2002;13-19
25. Yip E.C.H., Wong J.T.Y. Fluorescence activated cell-sorting of haemocytes in Penaeid prawns. Aquaculture. 204:2002;25-31
26. Sequeira T., Vilanova M., Lobo-da-Cunha A., Baldaia L., Arala-Chaves M. Flow cytometric analysis of molt-related changes in hemocyte type in male and female Penaeus japonicus. Biol Bull. 189:1995;376-380
27. Owens L., O'Neill A. Use of a clinical cell flow cytometer for differential counts of prawn Penaeus monodon haemocytes. Dis Aquat Organisms. 31:1997;147-153
28. Lüderitz O., Freudenberg M.A., Galanos C., Lehmann V., Rietschel E., Shaw D.H. Lipopolysaccharides of Gram-negative bacteria. Curr Top Membr Transp. 17:1982;79-151
29. Galanos C., Lüderitz O., Rietschel E., Westphal O., Brade H., Brade L., et al. Synthetic and natural Escherichia coli free lipid A express identical endotoxic activities. Eur J Biochem. 148:1985;1-5
30. Burrell R. Human responses to bacterial endotoxin. Circ Shock. 43:1994;137-153
31. Munford R.S., Hall C.L. Detoxification of bacterial lipopolysaccharides (endotoxins) by a human neutrophil enzyme. Science. 234:1986;203-205
32. Pohlman T.H., Munford R.S., Harlan J.M. Deacylated lipopolysaccharide inhibits neutrophil adherence to endothelium induced by lipopolysaccharide in vitro. J Exp Med. 165:1987;1393-1402
33. Lee S.Y., Söderhäll K. Early events in crustacean innate immunity. Fish Shellfish Immunol. 12:2002;421-437
34. Söderhäll K., Smith V.J., Johansson M.W. Exocytosis and uptake of bacteria by isolated haemocyte populations of two crustaceans: evidence for cellular co-operation in the defense reactions of arthropods. Cell Tissue Res. 245:1986;43-49
35. Charalambidis N., Zervas C., Lambropoulou M., Katsoris P., Marmaras V. Lipopolysaccharide-stimulated exocytosis of nonself recognition protein from insect hemocytes depend on protein tyrosine phosphorylation. Eur J Cell Biol. 67:1995;32-41
36. Charalambidis N., Foukas L., Zervas C., Marmaras V. Hemocyte surface phenoloxidase (PO) and immune response to lipopolysaccharide (LPS) in Ceratitis capitata. Insect Biochem Mol Biol. 26:1996;867-874
37. Darzynkiewicz Z., Juan G., Li X., Gorczyca W., Murakami T., Traganos F. Cytometry in cell necrobiology: analysis of apoptosis and accidental cell death (necrosis). Cytometry. 27:1997;1-20
38. Alikhani M., Alikhani Z., He H., Liu R., Popek B., Graves D. Lipopolysaccharides indirectly stimulate apoptosis and global induction of apoptotic genes in fibroblasts. J Biol Chem. 278:2003;52901-52908
39. Beck G., Cardinale S., Wang L., Reiner M., Sugumaran M. Characterization of a defense complex consisting of interleukin 1 and phenoloxidase from the hemolymph of the Tobacco hornworm, Manduca sexta. J Biol Chem. 271:1996;11035-11038
40. Ottaviani E., Franceschi C. The invertebrate phagocytic immunocyte: clues to a common evolution of immune and neuroendocrine systems. Immunol Today. 18:1997;169-174
41. Qureshi S., Larivière L., Leveque G., Clermont S., Moore K., Gros P., et al. Endotoxin-tolerant mice have mutations in Toll-like receptor 4 (Tlr4). J Exp Med. 189:1999;615-625
42. Song Y.L., Liu J.J., Chan L.C., Sung H.H. Glucan-induced disease resistance in tiger shrimp (Penaeus monodon). Dev Biol Standard. 90:1997;413-421
43. Chang C.F., Chen H.Y., Su M.S., Liao I.C. Immunomodulation by dietary beta-1,3-glucan in the brooders of the black tiger shrimp Penaeus monodon. Fish Shellfish Immunol. 10:2000;505-514
44. Sritunyalucksana K., Sithisarn P., Withayachumnarnkul B., Flegel T. Activation of prophenoloxidase, agglutinin and antibacterial activity in haemolymph of the black tiger prawn, Penaeus monodon, by immunostimulants. Fish Shellfish Immunol. 9:1999;21-30