Number of the records: 1  

Tick salivary cystatin sialostatin L2 suppresses IFN responses in mouse dendritic cells

  1. 1.
    SYSNO ASEP0453400
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleTick salivary cystatin sialostatin L2 suppresses IFN responses in mouse dendritic cells
    Author(s) Lieskovská, Jaroslava (BC-A) RID
    Páleníková, Jana (BC-A)
    Širmarová, J. (CZ)
    Elsterová, Jana (BC-A) ORCID
    Kotsyfakis, Michalis (BC-A) RID, ORCID
    Chagas, A. C. (US)
    Calvo, E. (US)
    Růžek, Daniel (BC-A) RID, ORCID
    Kopecký, Jan (BC-A) RID
    Source TitleParasite immunology. - : Wiley - ISSN 0141-9838
    Roč. 37, č. 2 (2015), s. 70-78
    Number of pages9 s.
    Publication formPrint - P
    Languageeng - English
    CountryGB - United Kingdom
    KeywordsTick ; Dendritic cells ; Interferon ; Cystatin
    Subject RIVEC - Immunology
    R&D ProjectsGAP302/12/2208 GA ČR - Czech Science Foundation (CSF)
    Institutional supportBC-A - RVO:60077344
    UT WOS000348718100002
    DOI10.1111/pim.12162
    AnnotationType I interferon (IFN), mainly produced by dendritic cells (DCs), is critical in the host defence against tick-transmitted pathogens. Here, we report that salivary cysteine protease inhibitor from the hard tick Ixodes scapularis, sialostatin L2, affects IFN- mediated immune reactions in mouse dendritic cells. Following IFN receptor ligation, the Janus activated kinases/signal transducer and activator of transcription (JAK/STAT) pathway is activated. We show that sialostatin L2 attenuates phosphorylation of STATs in spleen dendritic cells upon addition of recombinant IFN-. LPS-stimulated dendritic cells release IFN- which in turn leads to the induction of IFN-stimulated genes (ISG) through JAK/STAT pathway activation. The induction of two ISG, interferon regulatory factor 7 (IRF-7) and IP-10, was suppressed by sialostatin L2 in LPS-stimulated dendritic cells. Finally, the interference of sialostatin L2 with IFN action led to the enhanced replication of tick-borne encephalitis virus in DC. In summary, we present here that tick salivary cystatin negatively affects IFN- responses which may consequently increase the pathogen load after transmission via tick saliva.
    WorkplaceBiology Centre (since 2006)
    ContactDana Hypšová, eje@eje.cz, Tel.: 387 775 214
    Year of Publishing2016
Number of the records: 1  

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