Crosstalk of JNK1-STAT3 is critical for RAW264.7 cell survival
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
25269780
DOI
10.1016/j.cellsig.2014.09.013
PII: S0898-6568(14)00317-9
Knihovny.cz E-zdroje
- Klíčová slova
- Cell apoptosis, Cell survival pathway, Crosstalk, JAK/STAT, MAPK, T-2 toxin,
- MeSH
- anthraceny farmakologie MeSH
- apoptóza účinky léků MeSH
- biologické modely MeSH
- buněčné linie MeSH
- cytokiny genetika metabolismus MeSH
- fluorescenční protilátková technika MeSH
- fosforylace účinky léků MeSH
- Janus kinasy metabolismus MeSH
- kinetika MeSH
- makrofágy cytologie účinky léků metabolismus ultrastruktura MeSH
- mitochondrie účinky léků metabolismus ultrastruktura MeSH
- mitogenem aktivovaná proteinkinasa 8 metabolismus MeSH
- myši MeSH
- Ras proteiny metabolismus MeSH
- regulace genové exprese účinky léků MeSH
- ribozomy účinky léků metabolismus ultrastruktura MeSH
- signální transdukce * účinky léků MeSH
- T-2 toxin farmakologie MeSH
- transkripční faktor STAT3 metabolismus MeSH
- viabilita buněk účinky léků MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- anthraceny MeSH
- cytokiny MeSH
- Janus kinasy MeSH
- mitogenem aktivovaná proteinkinasa 8 MeSH
- pyrazolanthrone MeSH Prohlížeč
- Ras proteiny MeSH
- T-2 toxin MeSH
- transkripční faktor STAT3 MeSH
T-2 toxin, a major compound of trichothecenes, inhibits protein synthesis and induces inflammation and cell apoptosis through the activation of MAPK 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 treated with T-2 toxin. Our results revealed a crosstalk between JNK1 and STAT3 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 cells had been incubated with T-2 toxin for 12h. Our data suggest that T-2 toxin had a Janus face: it induced both apoptotic and cell survival pathways. These results suggest that the crosstalk and the balance between MAPK and JAK/STAT pathway might be involved in T-2 toxin-induced apoptosis in RAW264.7 cells.
Citace poskytuje Crossref.org
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