B. Novoa et al., IN-VITRO STUDIES ON THE REGULATION OF RAINBOW-TROUT (ONCORHYNCHUS-MYKISS) MACROPHAGE RESPIRATORY BURST ACTIVITY, Developmental and comparative immunology, 20(3), 1996, pp. 207-216
Modulation of the respiratory burst activity of head kidney macrophage
s isolated from rainbow trout (Oncorhynchus mykiss) was observed follo
wing treatment with several biologically active substances. Macrophage
-activating factor (MAF) induced the highest increment in respiratory
burst activity relative to treatment with lipopolysaccharide (LPS), tu
mor necrosis factor alpha (TNF alpha) or beta-glucans from Saccharomyc
es cerevisiae. Increased responses were more evident when these molecu
les were combined in pairs. Negative regulation of respiratory burst a
ctivity was observed when diMePGE(2) was added to the macrophages, wit
h maximal inhibition seen using a concentration of 2.6 mu M. Inhibitio
n was also seen using stimulated macrophages, either by co-incubation
of stimuli and diMePGE(2) or by adding diMePGE(2) to previously stimul
ated cells. The inhibitory effect on macrophages was detectable within
3 h of incubation with diMePGE(2) and by 24 h the level of the respon
se was even lower than that from unstimulated (control) macrophages. O
f significance was the finding that the inhibitory effect of prostagla
ndin on macrophage function could be overcome by co-incubation with st
imulatory molecules or by pre-treatment with MAF and LPS or MAF and TN
F alpha. Thus, the regulation of macrophage activation in fish is like
ly to be as complex as in mammals. Copyright (C) 1996 Elsevier Science
Ltd.