HIF-1α inhibits T-2 toxin-mediated "immune evasion" process by negatively regulating PD-1/PD-L1
Jazyk angličtina Země Irsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
36115646
DOI
10.1016/j.tox.2022.153324
PII: S0300-483X(22)00236-0
Knihovny.cz E-zdroje
- Klíčová slova
- HIF-1α, Hypoxia, Immune evasion, PD-1/PD-L1, T-2 toxin,
- MeSH
- antigeny CD274 metabolismus MeSH
- antigeny CD279 metabolismus MeSH
- faktor 1 indukovatelný hypoxií - podjednotka alfa farmakologie MeSH
- hypoxie MeSH
- lidé MeSH
- T-2 toxin * toxicita MeSH
- trichotheceny * toxicita MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- antigeny CD274 MeSH
- antigeny CD279 MeSH
- faktor 1 indukovatelný hypoxií - podjednotka alfa MeSH
- T-2 toxin * MeSH
- trichotheceny * MeSH
Trichothecene mycotoxins have a strong immunosuppressive effect, which may even escape host immune surveillance and damage the immune repair to show an "immune evasion" effect. Increasing lines of evidence have shown that hypoxia and hypoxia-inducible factors (HIFs) are key mediators of trichothecenes, and these toxins appear to be closely related to the "immune evasion" mechanisms. Therefore, we used RAW264.7 cell model to explore the association of T-2 toxins with "immune evasion" process and hypoxia, as well as their cross-linking effects induced by T-2 toxin. Our results showed that HIF-1α is an important toxicity target of T-2 toxin, which could induce intracellular hypoxia. T-2 toxin induced an "immune evasion" process by activating the PD-1/PD-L1 signaling pathway. Interestingly, when HIF-1α activation was blocked, the "immune evasion" process regulated by PD-1/PD-L1 signaling was activated, resulting in the cells damage, suggesting that hypoxia induced by T-2 toxin plays a protective role for RAW264.7 cell damage. Thus, our work shows that HIF-1α inhibits T-2 toxin-mediated "immune evasion" process by negatively regulating PD-1/PD-L1signaling. This study contributes to a better understanding of the immunotoxicity mechanism of trichothecenes.
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