Abstract

Leukotriene synthesis in neutrophils is critical for host survival during infection. In particular, leukotriene B4 (LTB4) is a powerful neutrophil chemoattractant that plays a crucial role in neutrophil swarming. In this work, we demonstrated that preincubation of human neutrophils with Salmonella typhimurium strongly stimulated LTB4 production induced by the bacterial chemoattractant, peptide N-formyl-L-methionyl-L-leucyl-l-phenylalanine (fMLP), while the reverse sequence of additions was ineffective. Preincubation with bacterial lipopolysaccharide or yeast polysaccharide zymosan particles gives weaker effect on fMLP-induced LTB4 production. Activation of 5-lipoxygenase (5-LOX), a key enzyme in leukotrienes biosynthesis, depends on rise of cytosolic concentration of Ca2+ and on translocation of the enzyme to the nuclear membrane. Both processes were stimulated by S. typhimurium. With an increase in the bacteria:neutrophil ratio, the transformation of LTB4 to ω-OH-LTB4 was suppressed, which further supported increased concentration of LTB4. These data indicate that in neutrophils gathered around bacterial clusters, LTB4 production is stimulated and at the same time its transformation is suppressed, which promotes neutrophil swarming and elimination of pathogens simultaneously.

Highlights

  • Neutrophils are the most abundant leukocytes circulating in mammalian blood

  • FMLP Boosts Leukotriene Synthesis in polymorphonuclear leukocytes (PMNLs) Pre-exposed to Bacteria

  • We observed a strong stimulation of leukotriene synthesis induced by formyl-peptide when neutrophils were preactivated by either opsonized (OS) or non-opsonized S. typhimurium (S)

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Summary

Introduction

Neutrophils (polymorphonuclear leukocytes, PMNLs) are the most abundant leukocytes circulating in mammalian blood. They are the first immune cells recruited by invading pathogens or damaged cells, playing a central role in both inflammation and host defense (Metschnikoff 1891; Kobayashi et al, 2018). N-formyl-L-methionyl-L-leucyl-L-phenylalanine (fMLP), a prototype N-formylated peptide, is a potent ligand for FPR1, a strong neutrophil chemoattractant, Bacteria Stimulate fMLP-Induced Leukotriene Synthesis and macrophage activator (Schiffmann et al, 1975; Snyderman and Pike 1984; Ye et al, 2009; Dorward et al, 2015; Dahlgren et al, 2016). FPRs play a critical role in defense against bacteria by recruiting inflammatory cells to sites of infection

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