All

What are you looking for?

All
Projects
Results
Organizations

Quick search

  • Projects supported by TA ČR
  • Excellent projects
  • Projects with the highest public support
  • Current projects

Smart search

  • That is how I find a specific +word
  • That is how I leave the -word out of the results
  • “That is how I can find the whole phrase”

Btk is a positive regulator in the TREM-1/DAP12 signaling pathway

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378050%3A_____%2F11%3A00370093" target="_blank" >RIV/68378050:_____/11:00370093 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1182/blood-2010-11-317016" target="_blank" >http://dx.doi.org/10.1182/blood-2010-11-317016</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1182/blood-2010-11-317016" target="_blank" >10.1182/blood-2010-11-317016</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Btk is a positive regulator in the TREM-1/DAP12 signaling pathway

  • Original language description

    TREM-1 receptor has been implicated in the production of proinflammatory cytokines and chemokines during bacterial infection and sepsis. For downstream signal transduction, TREM-1 is coupled to the ITAM-containing adaptor DAP12. We demonstrate that Bruton tyrosine kinase (Btk), becomes phosphorylated upon TREM-1 triggering. In cell lines, in which expression of Btk was diminished by shRNA-mediated knockdown, phosphorylation of Erk1/2 and PLC?1 and Ca+ mobilization were reduced after TREM-1 stimulation.TREM-1-induced production of the pro-inflammatory cytokines, TNF-? and IL-8, and up-regulation of activation/differentiation cell surface markers were impaired in Btk knockdown cells.Intact membrane localization and a functional kinase domain were required for TREM-1-mediated signaling. After TREM-1 engagement, TNF-? production by PBMCs was reduced in the patients suffering from XLA, a disease caused by mutations in the BTK gene.

  • 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

    <a href="/en/project/1M0506" target="_blank" >1M0506: Center of Molecular and Cellular Immunology</a><br>

  • Continuities

    Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2011

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Blood

  • ISSN

    0006-4971

  • e-ISSN

  • Volume of the periodical

    118

  • Issue of the periodical within the volume

    4

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    10

  • Pages from-to

    936-945

  • UT code for WoS article

    000293221700020

  • EID of the result in the Scopus database