4.5 Article

The Role of TLR2 and TLR4 in Recognition and Uptake of the Apicomplexan Parasite Eimeria bovis and Their Effects on NET Formation

期刊

PATHOGENS
卷 10, 期 2, 页码 -

出版社

MDPI
DOI: 10.3390/pathogens10020118

关键词

E. bovis; TLR; IL-8; neutrophil extracellular traps

资金

  1. DFG [216337519 (TA291/4-1)]
  2. Institute of Parasitology (Justus Liebig University Giessen)
  3. Department of Pathobiology and Population Sciences, Royal Veterinary College, Hawkshead Lane, UK
  4. FONDECYT. from the National Research and Development Agency of Chile (ANID) [11200103]
  5. European Research Development Fund
  6. Welsh Government

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This study found that during bovine PMN-derived NETosis induced by E. bovis, both TLR2 and TLR4 were upregulated, while not significantly affecting phagocytosis of sporozoites. However, it enhanced IL-8 production, with TLR2 inducing stronger NF-kappa B activation compared to TLR4. Immunofluorescence analysis confirmed TLR expression on PMN and concurrent NET formation.
Background: Bovine polymorphonuclear neutrophils (PMN) constitutively express the Toll-like receptors (TLRs) TLR2 and TLR4 and have been shown to generate Neutrophil extracellular traps (NETs) upon exposure to Eimeria bovis. The present work investigated the role of TLR2 and TLR4 in the recognition and uptake of E. bovis sporozoites, IL-8 production and neutrophil extracellular trap (NET) formation. Methods: TLR expression was performed by flow cytometric analysis on PMN exposed to live carboxyfluorescein succinimidyl ester (CFSE)-stained sporozoites. Supernatants of PMN exposed to different E. bovis sporozoite preparations and antigens in the absence or presence of TLR antibodies were assessed for IL-8 secretion. Cells were exposed to sporozoite preparations and assessed for the activation of transcription factor NF-kappa B using a luciferase reporter assay. Immunofluorescence analysis was done to investigate TLR2 and TLR4 surface expression and NET formation on bovine PMN exposed to vital sporozoites. Results: we observed significantly increased TLR2 and TLR4 expression with a mean increase in expression that was greater for TLR2 than TLR4. This upregulation neither inhibited nor promoted sporozoite phagocytosis by bovine PMN. Live sporozoites together with anti-TLR2 mAb resulted in a significant enhancement of IL-8 production. NF-kappa B activation was more strongly induced in TLR2-HEK cells than in TLR4/MD2-HEK cells exposed to heat-killed sporozoites and antigens. Immunofluorescence analysis showed TLR-positive signals on the surface of PMN and concomitant NET formation. Conclusions: This is the first report on E. bovis-induced concomitant TLR2 and TLR4 expression during bovine PMN-derived NETosis.

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