Matches in SemOpenAlex for { <https://semopenalex.org/work/W2040397671> ?p ?o ?g. }
- W2040397671 endingPage "e62016" @default.
- W2040397671 startingPage "e62016" @default.
- W2040397671 abstract "Background β-glucans are fungal cell wall components that bind to the C-type lectin-like receptor dectin-1. Polymorphisms of dectin-1 gene are associated with susceptibility to invasive fungal infection and medically refractory ulcerative colitis. The purpose of this study has been addressing the response of human macrophages to β-glucans under different conditions mimicking the composition of the inflammatory milieu in view of the wide plasticity and large range of phenotypical changes showed by these cells, and the relevant role of dectin-1 in several pathophysiological conditions. Principal Findings Serum-differentiated macrophages stimulated with β-glucans showed a low production of TNFα and IL-1β, a high production of IL-6 and IL-23, and a delayed induction of cyclooxygenase-2 and PGE2 biosynthesis that resembled the responses elicited by crystals and those produced when phagosomal degradation of the phagocytic cargo increases ligand access to intracellular pattern recognition receptors. Priming with a low concentration of LPS produced a rapid induction of cyclooxygenase-2 and a synergistic release of PGE2. When the differentiation of the macrophages was carried out in the presence of M-CSF, an increased expression of dectin-1 B isoform was observed. In addition, this treatment made the cells capable to release arachidonic acid in response to β-glucan. Conclusions These results indicate that the macrophage response to fungal β-glucans is strongly influenced by cytokines and microbial-derived factors that are usual components of the inflammatory milieu. These responses can be sorted into three main patterns i) an elementary response dependent on phagosomal processing of pathogen-associated molecular patterns and/or receptor-independent, direct membrane binding linked to the immunoreceptor tyrosine-based activation motif-bearing transmembrane adaptor DNAX-activating protein 12, ii) a response primed by TLR4-dependent signals, and iii) a response dependent on M-CSF and dectin-1 B isoform expression that mainly signals through the dectin-1 B/spleen tyrosine kinase/cytosolic phospholipase A2 route." @default.
- W2040397671 created "2016-06-24" @default.
- W2040397671 creator A5000201213 @default.
- W2040397671 creator A5010023676 @default.
- W2040397671 creator A5012402337 @default.
- W2040397671 creator A5020817430 @default.
- W2040397671 creator A5030862473 @default.
- W2040397671 creator A5050059516 @default.
- W2040397671 creator A5056326228 @default.
- W2040397671 creator A5071725389 @default.
- W2040397671 creator A5076681797 @default.
- W2040397671 date "2013-04-24" @default.
- W2040397671 modified "2023-10-18" @default.
- W2040397671 title "The Response of Human Macrophages to β-Glucans Depends on the Inflammatory Milieu" @default.
- W2040397671 cites W1482682744 @default.
- W2040397671 cites W1610489281 @default.
- W2040397671 cites W1674996329 @default.
- W2040397671 cites W1766651653 @default.
- W2040397671 cites W1964465182 @default.
- W2040397671 cites W1985347885 @default.
- W2040397671 cites W1987044793 @default.
- W2040397671 cites W1989968940 @default.
- W2040397671 cites W1993162037 @default.
- W2040397671 cites W1994603967 @default.
- W2040397671 cites W1994671525 @default.
- W2040397671 cites W1999099522 @default.
- W2040397671 cites W2004644593 @default.
- W2040397671 cites W2006061916 @default.
- W2040397671 cites W2023989156 @default.
- W2040397671 cites W2024392158 @default.
- W2040397671 cites W2036743290 @default.
- W2040397671 cites W2048844594 @default.
- W2040397671 cites W2051185006 @default.
- W2040397671 cites W2059344017 @default.
- W2040397671 cites W2063668813 @default.
- W2040397671 cites W2069360787 @default.
- W2040397671 cites W2075913925 @default.
- W2040397671 cites W2085746003 @default.
- W2040397671 cites W2086524434 @default.
- W2040397671 cites W2088903425 @default.
- W2040397671 cites W2089430148 @default.
- W2040397671 cites W2099874350 @default.
- W2040397671 cites W2101524137 @default.
- W2040397671 cites W2103322081 @default.
- W2040397671 cites W2107531246 @default.
- W2040397671 cites W2111219358 @default.
- W2040397671 cites W2111717604 @default.
- W2040397671 cites W2119104273 @default.
- W2040397671 cites W2119252911 @default.
- W2040397671 cites W2126924404 @default.
- W2040397671 cites W2128850053 @default.
- W2040397671 cites W2140333814 @default.
- W2040397671 cites W2143498880 @default.
- W2040397671 cites W2162444234 @default.
- W2040397671 cites W2170191276 @default.
- W2040397671 cites W2172216021 @default.
- W2040397671 cites W4313341523 @default.
- W2040397671 doi "https://doi.org/10.1371/journal.pone.0062016" @default.
- W2040397671 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3634770" @default.
- W2040397671 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/23637950" @default.
- W2040397671 hasPublicationYear "2013" @default.
- W2040397671 type Work @default.
- W2040397671 sameAs 2040397671 @default.
- W2040397671 citedByCount "38" @default.
- W2040397671 countsByYear W20403976712013 @default.
- W2040397671 countsByYear W20403976712014 @default.
- W2040397671 countsByYear W20403976712015 @default.
- W2040397671 countsByYear W20403976712016 @default.
- W2040397671 countsByYear W20403976712017 @default.
- W2040397671 countsByYear W20403976712018 @default.
- W2040397671 countsByYear W20403976712019 @default.
- W2040397671 countsByYear W20403976712020 @default.
- W2040397671 countsByYear W20403976712021 @default.
- W2040397671 countsByYear W20403976712022 @default.
- W2040397671 countsByYear W20403976712023 @default.
- W2040397671 crossrefType "journal-article" @default.
- W2040397671 hasAuthorship W2040397671A5000201213 @default.
- W2040397671 hasAuthorship W2040397671A5010023676 @default.
- W2040397671 hasAuthorship W2040397671A5012402337 @default.
- W2040397671 hasAuthorship W2040397671A5020817430 @default.
- W2040397671 hasAuthorship W2040397671A5030862473 @default.
- W2040397671 hasAuthorship W2040397671A5050059516 @default.
- W2040397671 hasAuthorship W2040397671A5056326228 @default.
- W2040397671 hasAuthorship W2040397671A5071725389 @default.
- W2040397671 hasAuthorship W2040397671A5076681797 @default.
- W2040397671 hasBestOaLocation W20403976711 @default.
- W2040397671 hasConcept C100701293 @default.
- W2040397671 hasConcept C111289621 @default.
- W2040397671 hasConcept C136449434 @default.
- W2040397671 hasConcept C170493617 @default.
- W2040397671 hasConcept C181199279 @default.
- W2040397671 hasConcept C202751555 @default.
- W2040397671 hasConcept C203014093 @default.
- W2040397671 hasConcept C2775858924 @default.
- W2040397671 hasConcept C2776352991 @default.
- W2040397671 hasConcept C2776914184 @default.
- W2040397671 hasConcept C2777700362 @default.
- W2040397671 hasConcept C2778078955 @default.