Published in

Elsevier, Veterinary Immunology and Immunopathology, 2-4(139), p. 308-312, 2011

DOI: 10.1016/j.vetimm.2010.10.021

Links

Tools

Export citation

Search in Google Scholar

Induction of reactive oxygen species in bovine neutrophils is CD11b, but not dectin-1-dependent

Journal article published in 2011 by I. Conejeros, R. Patterson, R. A. Burgos, C. Hermosilla, D. Werling ORCID
This paper is available in a repository.
This paper is available in a repository.

Full text: Download

Green circle
Preprint: archiving allowed
Orange circle
Postprint: archiving restricted
Red circle
Published version: archiving forbidden
Data provided by SHERPA/RoMEO

Abstract

Neutrophils play a key role in initiating an innate immune response, being the first type of immune cell arriving at the site of injury or infection. These cells are able to mount a direct anti-bactericidal response by the production of reactive oxygen or reactive nitrogen species (ROS/RNS). An important component of the host innate immune response is recognition of pathogen-associated molecular patterns (PAMPs) by pattern recognition receptors (PRRs). Toll-like receptors (TLRs) are an important family of PRRs and, are a key component in activation of innate immune mechanisms. In the present study we described the presence of mRNA transcripts for TLR1, TLR2, TLR4, TLR6, TLR7 and TLR10 in bovine neutrophils. In contrast, the presence of mRNA transcripts for TLR3 varied between animals, whereas no transcripts were detected for TLR5, TLR8, TLR9 or the C-type lectin receptor dectin-1 in neutrophils isolated from bovine blood. Additionally, zymosan, a dectin-1/TLR2 ligand, induced ROS, but not RNS production in a CD11b-, but not dectin-1-dependent manner. This effect was dependent on Store Operated Calcium Entry (SOCE), and partially inhibited using monoclonal antibodies to CD11b. Taken together, our data describe the presence of specific PRRs transcripts in the mRNA isolated from bovine neutrophil and show a CD11b-/Ca(2+) dependent ROS production by these cells.