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Transmembrane adaptor protein TRIM regulates T cell receptor (TCR) expression and TCR-mediated signaling via an association with the TCR zeta chain.

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378050%3A_____%2F01%3A23010293" target="_blank" >RIV/68378050:_____/01:23010293 - isvavai.cz</a>

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Transmembrane adaptor protein TRIM regulates T cell receptor (TCR) expression and TCR-mediated signaling via an association with the TCR zeta chain.

  • Original language description

    Adaptor protein TRIM preferentially interacts with the TCRvia the TCR-y and CD3-eg. Overexpression of TRIM cells results in enhancement of TCR expression and elevated induction of Ca(2+) mobilization. TRIM-mediated upregulation of TCR expression resultsfrom inhibition of spontaneous TCR internalization of TCR complexes on the cell surface. TRIM is a novel component of the TCR complex modulating the strength of TCR signals through regulation of TCR expression on the cell surface.

  • 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/GA204%2F99%2F0367" target="_blank" >GA204/99/0367: Molecular mechanisms of signalling through immunoreceptors</a><br>

  • Continuities

    Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2001

  • 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 Experimental Medicine

  • ISSN

    0022-1007

  • e-ISSN

  • Volume of the periodical

    193

  • Issue of the periodical within the volume

    11

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    15

  • Pages from-to

    1269-1283

  • UT code for WoS article

  • EID of the result in the Scopus database