Tj. Brazil et al., PRIMING INDUCES FUNCTIONAL COUPLING OF N-FORMYL-METHIONYL-LEUCYL-PHENYLALANINE RECEPTORS IN EQUINE NEUTROPHILS, Journal of leukocyte biology, 63(3), 1998, pp. 380-388
The synthetic formylpeptide fMLP is widely used as a model chemoattrac
tant and secretagogue for mammalian neutrophils. Despite possessing fM
LP receptors, equine neutrophils do not produce superoxide anions in r
esponse to fMLP and there is no inflammatory reaction in the horse whe
n fMLP is injected intradermally. The functional capability of these r
eceptors was investigated after pretreatment with recognized priming a
gents, Purified neutrophils were pretreated with lipopolysaccharide (L
PS), platelet-activating factor (PAF), or tumor necrosis factor alpha
(TNF-alpha) and superoxide anion generation and shape clange quantifie
d by lucigenin-dependent chemiluminescence (LDCL) and flow cytometry,
respectively. LPS, TNF-alpha, and PAF pretreatment induced significant
LDCL in response to fMLP; similarly LPS pretreatment was a prerequisi
te for fMLP-stimulated neutrophil polarization in response to fMLP. Ho
wever, LPS failed to induce fMLP-mediated chemotaxis of equine neutrop
hils. These data indicate that equine neutrophil fMLP receptors are no
t vestigial as previously thought but can trigger both respiratory bur
st activity and cell polarization responses after priming.