TLR4-mediated release of heparin-binding protein in human airways: a co-stimulatory role for IL-26

• Published in: Frontiers in immunology Vol. 14; p. 1178135
• Main Authors: Paulsson, Magnus, Cardenas, Eduardo I, Che, Karlhans F, Brundin, Bettina, Smith, Margaretha, Qvarfordt, Ingemar, Lindén, Anders
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Media S.A 2023
• Subjects: Adjuvants, Immunologic; azurocidin; Blood Proteins - metabolism; CAP37; Carrier Proteins - metabolism; cells; Clinical Medicine; heparin-binding protein (HBP); Humans; identification; IL-26; Immunologi inom det medicinska området; Immunology; Immunology in the medical area; infection; Infectious Medicine; Infektionsmedicin; interleukin-26; Klinisk medicin; lipopolysaccharide; lipopolysaccharide (LPS); Lipopolysaccharides - pharmacology; Medical and Health Sciences; Medicin och hälsovetenskap; monocytes; neutrophil recruitment; neutrophils; receptor 4 (TLR4); secretion; survival; toll-like; toll-like receptor 4 (TLR4); Toll-Like Receptor 4 - metabolism; lipopolysaccharide (LPS); azurocidin; heparin-binding protein (HBP); CAP37; IL-26; toll-like receptor 4 (TLR4); neutrophils
• ISSN: 1664-3224; 1664-3224
• DOI: 10.3389/fimmu.2023.1178135

Bacterial infection causes accumulation of neutrophils that release antimicrobial proteins including heparin-binding protein (HBP). In human airways, this neutrophil accumulation can be re-capitulated via intrabronchial exposure to lipopolysaccharide (LPS), a Toll-like receptor 4 (TLR4) agonist, that also causes a local increase in the neutrophil-mobilizing cytokine IL-26. Although LPS is considered a weak stimulus for HBP release , its effect on HBP release in human airways has not been characterized. We determined whether intrabronchial exposure to LPS causes concomitant release of HBP and IL-26 in human airways, and whether IL-26 can enhance LPS-induced release of HBP in isolated human neutrophils. We found that the concentration of HBP was markedly increased in bronchoalveolar lavage (BAL) fluid 12, 24, and 48 hours after LPS exposure, and that it displayed a strong and positive correlation with that of IL-26. Moreover, the concentration of HBP in conditioned media from isolated neutrophils was enhanced only after co-stimulation with LPS and IL-26. Taken together, our findings indicate that TLR4 stimulation causes concomitant release of HBP and IL-26 in human airways, and that IL-26 may constitute a required co-stimulant for HBP release in neutrophils, thus enabling the concerted action of HBP and IL-26 in local host defense.