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Crosstalk of JNK1-STAT3 is critical for RAW264.7 cell survival

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F62690094%3A18450%2F14%3A50002644" target="_blank" >RIV/62690094:18450/14:50002644 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.cellsig.2014.09.013" target="_blank" >http://dx.doi.org/10.1016/j.cellsig.2014.09.013</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.cellsig.2014.09.013" target="_blank" >10.1016/j.cellsig.2014.09.013</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Crosstalk of JNK1-STAT3 is critical for RAW264.7 cell survival

  • Original language description

    T-2 toxin, a major compound of trichothecenes, inhibits protein synthesis and induces inflammation and cell apoptosis through the activation ofMAPK pathway. The JAK/STAT pathway has recently been shown to be downstream targets of trichothecenes. However,whether there is any crosstalk between JNK and JAK/STAT pathways in trichothecene toxicity has not been studied. In the present study, we explored this potential in RAW264.7 cells treatedwith T-2 toxin. Our results revealed a crosstalk between JNK1 andSTAT3 after T-2 toxin treatment,which was mediated by K-Ras. T-2 toxin treatment resulted in rapid phosphorylation, and more importantly, JNK1- STAT3 signaling pathway was shown to maintain the normal function of the mitochondria and to inhibit T-2 toxin-induced apoptosis. Therefore, this pathway was considered to be a potential cell survival pathway. Breakdown and degranulation of ribosomes in the rough endoplasmic reticulum and swelling of mitochondria were clearly visible after the ce

  • Czech name

  • Czech description

Classification

  • Type

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

  • CEP classification

    FP - Other medical fields

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2014

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Cellular signalling

  • ISSN

    0898-6568

  • e-ISSN

  • Volume of the periodical

    26

  • Issue of the periodical within the volume

    12

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    10

  • Pages from-to

    2951-2960

  • UT code for WoS article

    000345107700040

  • EID of the result in the Scopus database