Influence of technical parameters on the in vitro motility of equine neutrophils in the presence of streptococcal culture supernatant

• Published in: Veterinary immunology and immunopathology Vol. 23; no. 1; pp. 85 - 101
• Main Authors: Blancquaert, Anne-Marie B., Colgan, Sean P., Bruyninckx, Walter J.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 30.11.1989
• Subjects: Animals; CABALLOS; Cell Count; Chemotaxis, Leukocyte - immunology; CHEVAL; Culture Media; Enterococcus faecalis - immunology; FAGOCITOS; Female; Gelatin; HORSES; Horses - immunology; Immunologic Techniques; In Vitro Techniques; LEUCOCITOS; LEUCOCYTE; LEUKOCYTES; Neutrophils - immunology; PHAGOCYTE; PHAGOCYTES; Sepharose; STREPTOCOCCUS; Time Factors
• ISSN: 0165-2427; 1873-2534
• DOI: 10.1016/0165-2427(89)90112-8

To identify the influence of technical factors on the in vitro motility of equine neutrophils towards streptococcus culture supernatant in an under-agarose assay, we studied the changes in eight cell migration parameters. The distances the phagocytes travelled by directed, random and spontaneous migration increased with incubation time, cell concentration and the gelatin and serum contents of the migration plates. The contribution of chemotaxis to the phagocyte migrations, however, decreased simultaneously. The directed and random, though not the spontaneous, migrations of the phagocytes increased also when the chemoattractant wells were placed closer to the cell wells but so did the influence of the chemokinetic activity of the bacterial culture supernatant on phagocyte motility. In contrast, preincubation of migration plates with the chemoattractant, the agarose content of the migration plates and contamination of the granulocytes with non-migrating, mononuclear cells did not substantially affect the in vitro migrations of the neutrophils. The changes in the in vitro motility of the equine neutrophils by these technical factors were, in general, comparable to those reported for human cells attracted by a variety of host- and bacteria-derived chemoattractants.