Crosstalk of JNK1-STAT3 is critical for RAW264.7 cell survival
Language English Country England, Great Britain Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
25269780
DOI
10.1016/j.cellsig.2014.09.013
PII: S0898-6568(14)00317-9
Knihovny.cz E-resources
- Keywords
- Cell apoptosis, Cell survival pathway, Crosstalk, JAK/STAT, MAPK, T-2 toxin,
- MeSH
- Anthracenes pharmacology MeSH
- Apoptosis drug effects MeSH
- Models, Biological MeSH
- Cell Line MeSH
- Cytokines genetics metabolism MeSH
- Fluorescent Antibody Technique MeSH
- Phosphorylation drug effects MeSH
- Janus Kinases metabolism MeSH
- Kinetics MeSH
- Macrophages cytology drug effects metabolism ultrastructure MeSH
- Mitochondria drug effects metabolism ultrastructure MeSH
- Mitogen-Activated Protein Kinase 8 metabolism MeSH
- Mice MeSH
- ras Proteins metabolism MeSH
- Gene Expression Regulation drug effects MeSH
- Ribosomes drug effects metabolism ultrastructure MeSH
- Signal Transduction * drug effects MeSH
- T-2 Toxin pharmacology MeSH
- STAT3 Transcription Factor metabolism MeSH
- Cell Survival drug effects MeSH
- Animals MeSH
- Check Tag
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Anthracenes MeSH
- Cytokines MeSH
- Janus Kinases MeSH
- Mitogen-Activated Protein Kinase 8 MeSH
- pyrazolanthrone MeSH Browser
- ras Proteins MeSH
- T-2 Toxin MeSH
- STAT3 Transcription Factor 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.
References provided by Crossref.org
Selective inhibitors for JNK signalling: a potential targeted therapy in cancer
Antioxidant agents against trichothecenes: new hints for oxidative stress treatment