1. Agaphelin modulates the activation of human bronchial epithelial cells induced by lipopolysaccharide and IL-4.
- Author
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Favarin DC, Pereira ABM, Francischetti IMB, da Silva MV, Rodrigues V Jr, da Silva PR, Valenzuela JG, Teixeira DNS, Oliveira CJF, and Rogério AP
- Subjects
- Biomarkers, Cytokines metabolism, Epithelial Cells drug effects, Epithelial Cells metabolism, Humans, Protein Binding, STAT1 Transcription Factor metabolism, Signal Transduction, Toll-Like Receptor 4 metabolism, Anti-Inflammatory Agents pharmacology, Insect Proteins pharmacology, Interleukin-4 metabolism, Lipopolysaccharides immunology, Respiratory Mucosa immunology, Respiratory Mucosa metabolism, Salivary Proteins and Peptides pharmacology
- Abstract
Sand fly saliva presents molecules with potential to development of compounds for treatment of inflammatory diseases. Agaphelin, isolated from the saliva of the mosquito Anopheles gambiae, demonstrates anti-inflammatory properties such as neutrophils chemotaxis inhibition. Here, we extend these results and evaluated the role of agaphelin (0.1-100 nM) in an in vitro model consisting in the activation of human bronchial epithelial cells (BEAS-2B) by IL-4 (50 ng/mL) or lipopolysaccharide (LPS; 10 ng/mL). Agaphelin is non-cytotoxic for BEAS-2B cells. Notably, agaphelin markedly reduces CCL2 and IL-8 production induced by IL-4 or LPS, without altering the IL-10 production. The TLR4 expression and STAT1 phosphorylation induced by LPS were inhibited by agaphlin. In addition, agaphelin decreased the phosphorylation of STAT6 induce by IL-4, whose effect was independent of IL-4-binding activity. Taken together, these findings identify agaphelin as a potential anti-inflammatory therapeutic agent for airway inflammations., Competing Interests: Declaration of Competing Interest The authors declare that they have no conflict of interest., (Copyright © 2020 Elsevier GmbH. All rights reserved.)
- Published
- 2020
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