HIF-1α is a "brake" in JNK-mediated activation of amyloid protein precursor and hyperphosphorylation of tau induced by T-2 toxin in BV2 cells
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články
PubMed
38319535
DOI
10.1007/s12550-024-00525-6
PII: 10.1007/s12550-024-00525-6
Knihovny.cz E-zdroje
- Klíčová slova
- Amyloid precursor protein, Hypoxia-inducible factor-1α, T-2 toxin, Tau, c-Jun N-terminal kinase,
- MeSH
- amyloidový prekurzorový protein beta * metabolismus MeSH
- buněčné linie MeSH
- faktor 1 indukovatelný hypoxií - podjednotka alfa * metabolismus genetika MeSH
- fosforylace účinky léků MeSH
- JNK mitogenem aktivované proteinkinasy metabolismus MeSH
- myši MeSH
- proteiny tau * metabolismus MeSH
- signální transdukce účinky léků MeSH
- T-2 toxin * toxicita MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- amyloidový prekurzorový protein beta * MeSH
- faktor 1 indukovatelný hypoxií - podjednotka alfa * MeSH
- Hif1a protein, mouse MeSH Prohlížeč
- JNK mitogenem aktivované proteinkinasy MeSH
- proteiny tau * MeSH
- T-2 toxin * MeSH
Mycotoxins have been shown to activate multiple mechanisms that may potentially lead to the progression of Alzheimer's disease (AD). Overexpression/aberrant cleavage of amyloid precursor protein (APP) and hyperphosphorylation of tau (P-tau) is hallmark pathologies of AD. Recent advances suggest that the neurotoxic effects of mycotoxins involve c-Jun N-terminal kinase (JNK) and hypoxia-inducible factor-1α (HIF-1α) signaling, which are closely linked to the pathogenesis of AD. Due to the high toxicity and broad contamination of T-2 toxin, we assessed how T-2 toxin exposure alters APP and P-tau formation in BV2 cells and determined the underlying roles of HIF-1α and JNK signaling. The findings revealed that T-2 toxin stimulated the expression of HIF-1α and hypoxic stress factors in addition to increasing the expression of APP and P-tau. Additionally, HIF-1α acted as a "brake" on the induction of APP and P-tau expression by negatively regulating these proteins. Notably, T-2 toxin activated JNK signaling, which broke this "brake" to promote the formation of APP and P-tau. Furthermore, the cytoskeleton was an essential target for T-2 toxin to exert cytotoxicity, and JNK/HIF-1α participated in this damage. Collectively, when the T-2 toxin induces the production of APP and P-tau, JNK might interfere with HIF-1α's protective function. This study will provide clues for further research on the neurotoxicity of mycotoxins.
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