Calcineurin inhibitors reduce NFAT-dependent expression of antifungal pentraxin-3 by human monocytes
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00159816%3A_____%2F20%3A00072951" target="_blank" >RIV/00159816:_____/20:00072951 - isvavai.cz</a>
Alternative codes found
RIV/00216224:14110/20:00115426
Result on the web
<a href="https://jlb.onlinelibrary.wiley.com/doi/full/10.1002/JLB.4VMA0318-138R" target="_blank" >https://jlb.onlinelibrary.wiley.com/doi/full/10.1002/JLB.4VMA0318-138R</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1002/JLB.4VMA0318-138R" target="_blank" >10.1002/JLB.4VMA0318-138R</a>
Alternative languages
Result language
angličtina
Original language name
Calcineurin inhibitors reduce NFAT-dependent expression of antifungal pentraxin-3 by human monocytes
Original language description
Calcineurin (CN) inhibitors are effective clinical immunosuppressants but leave patients vulnerable to potentially fatal fungal infections. This study tested the hypothesis that CN inhibition interferes with antifungal immune defenses mediated by monocytes. We showed that NFAT is expressed by human monocytes, and is activated by exposure to fungal ligands. We confirmed that NFAT translocation potently activated target gene transcription using a human monocytic reporter cell line. Inhibition of CN-NFAT by cyclosporine A significantly reduced monocyte production of TNF-alpha, IL-10, and MCP-1 proteins in response to pattern recognition receptor ligands as well as to Aspergillus fumigatus conidia. Moreover, we revealed that human monocytes express the antifungal protein pentraxin-3 under control of NFAT. In conclusion, clinical CN inhibitors have the potential to interfere with the novel NFAT-dependent pentraxin-3 pathway as well as antifungal cytokine production in human monocytes, thereby impeding monocyte-mediated defenses against fungal infection in immune-suppressed patients.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10601 - Cell biology
Result continuities
Project
Result was created during the realization of more than one project. More information in the Projects tab.
Continuities
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Others
Publication year
2020
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Journal of leukocyte biology
ISSN
0741-5400
e-ISSN
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Volume of the periodical
107
Issue of the periodical within the volume
3
Country of publishing house
US - UNITED STATES
Number of pages
12
Pages from-to
497-508
UT code for WoS article
000515440500012
EID of the result in the Scopus database
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