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Nonredundant roles of Src-family kinases and Syk in the initiation of B-cell antigen receptor signaling

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378050%3A_____%2F13%3A00398758" target="_blank" >RIV/68378050:_____/13:00398758 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.4049/jimmunol.1202401" target="_blank" >http://dx.doi.org/10.4049/jimmunol.1202401</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.4049/jimmunol.1202401" target="_blank" >10.4049/jimmunol.1202401</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Nonredundant roles of Src-family kinases and Syk in the initiation of B-cell antigen receptor signaling

  • Original language description

    When a BCR on a mature B cell is engaged by its ligand, the cell becomes activated, and the Ab-mediated immune response can be triggered. The initiation of BCR signaling is orchestrated by kinases of the Src and Syk families. However, the proximal BCR-induced phosphorylation remains incompletely understood. According to a model of sequential activation of kinases, Syk acts downstream of Src family kinases (SFKs). In addition, signaling independent of SFKs and initiated by Syk has been proposed. Both hypotheses lack sufficient evidence from relevant B cell models, mainly because of the redundancy of Src family members and the importance of BCR signaling for B cell development. We addressed this issue by analyzing controlled BCR triggering ex vivo on primary murine B cells and on murine and chicken B cell lines. Chemical and Csk-based genetic inhibitor treatments revealed that SFKs are required for signal initiation and Syk activation. In addition, ligand and anti-BCR Ab-induced signalin

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    EB - Genetics and molecular biology

  • OECD FORD branch

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

    2013

  • 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 Immunology

  • ISSN

    0022-1767

  • e-ISSN

  • Volume of the periodical

    190

  • Issue of the periodical within the volume

    4

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    12

  • Pages from-to

    1807-1818

  • UT code for WoS article

    000314825400044

  • EID of the result in the Scopus database