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Calcineurin-NFAT signaling controls neutrophils' ability of chemoattraction upon fungal infection

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00023736%3A_____%2F24%3A00013728" target="_blank" >RIV/00023736:_____/24:00013728 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216224:14110/24:00139184 RIV/00159816:_____/24:00081026

  • Result on the web

    <a href="https://doi.org/10.1093/jleuko/qiae091" target="_blank" >https://doi.org/10.1093/jleuko/qiae091</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1093/jleuko/qiae091" target="_blank" >10.1093/jleuko/qiae091</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Calcineurin-NFAT signaling controls neutrophils' ability of chemoattraction upon fungal infection

  • Original language description

    Calcineurin-nuclear factor of activated T cells (CN-NFAT) inhibitors are widely clinically used drugs for immunosuppression, but besides their required T cell response inhibition, they also undesirably affect innate immune cells. Disruption of innate immune cell function can explain the observed susceptibility of CN-NFAT inhibitor-treated patients to opportunistic fungal infections. Neutrophils play an essential role in innate immunity as a defense against pathogens, however, the effect of CN-NFAT inhibitors on neutrophil function was poorly described. Thus, we tested the response of human neutrophils to opportunistic fungal pathogens, namely Candida albicans and Aspergillus fumigatus, in the presence of CN-NFAT inhibitors. Here, we report that the NFAT pathway members were expressed in neutrophils and mediated part of the neutrophil response to pathogens. Upon pathogen exposure, neutrophils underwent profound transcriptomic changes with subsequent production of effector molecules. Importantly, genes and proteins involved in the regulation of the immune response and chemotaxis, including the chemokines CCL2, CCL3, and CCL4 were significantly upregulated. The presence of CN-NFAT inhibitors attenuated the expression of these chemokines and impaired the ability of neutrophils to chemoattract other immune cells. Our results amend knowledge about the impact of CN-NFAT inhibition in human neutrophils.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    30205 - Hematology

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2024

  • 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

  • Volume of the periodical

    116

  • Issue of the periodical within the volume

    4

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    14

  • Pages from-to

    816-829

  • UT code for WoS article

    001217258900001

  • EID of the result in the Scopus database

    2-s2.0-85202912440