Journalartikel

IRE1 and PERK signaling regulates inflammatory responses in a murine model of contact hypersensitivity


AutorenlisteGendrisch, Fabian; Voelkel, Lukas; Fluck, Melanie; Apostolova, Petya; Zeiser, Robert; Jakob, Thilo; Martin, Stefan F.; Esser, Philipp R.

Jahr der Veröffentlichung2022

Seiten966-978

ZeitschriftAllergy

Bandnummer77

Heftnummer3

ISSN0105-4538

eISSN1398-9995

DOI Linkhttps://doi.org/10.1111/all.15024

VerlagWiley


Abstract
Background Contact sensitizers may interfere with correct protein folding. Generation of un-/misfolded proteins can activate the IRE-1 or PERK signaling pathways initiating the unfolded protein response (UPR) and thereby determine inflammatory immune responses. We have analyzed the effect of sensitizers with different potencies on the induction of UPR activation/inhibition and the subsequent generation of a pro-inflammatory micromilieu in vitro as well as the effect of UPR modulation on the inflammatory response in the murine contact hypersensitivity (CHS) in vivo. Methods Semi-quantitative and quantitative PCR, fluorescence microscopy, ELISA, NF-kappa B activation and translocation assays, DC/keratinocyte co-culture assay, FACS, and in vivo CHS experiments were performed. Results Sensitizers and irritants activate IRE-1 and PERK in murine and human keratinocytes. Synergistic effects occur after combination of different weak sensitizers / addition of irritants. Moreover, tolerogenic dinitrothiocyanobenzene can be converted into a strong sensitizer by pre-activation of the UPR. Blocking UPR signaling results in decreased NF-kappa B activation and cytokine production in keratinocytes and in activation marker downregulation in a HaCaT/THP-1 co-culture. Interestingly, not only systemic but also topical application of UPR inhibitors abrogates CHS responses in vivo. Conclusion These observations highlight an important role of the UPR in determination of the inflammatory response in vitro and in vivo further underlining the importance of tissue stress and damage responses in the development of ACD and provide mechanistically based concepts as a basis for the development of new therapeutic approaches to treat allergic contact dermatitis.



Zitierstile

Harvard-ZitierstilGendrisch, F., Voelkel, L., Fluck, M., Apostolova, P., Zeiser, R., Jakob, T., et al. (2022) IRE1 and PERK signaling regulates inflammatory responses in a murine model of contact hypersensitivity, Allergy, 77(3), pp. 966-978. https://doi.org/10.1111/all.15024

APA-ZitierstilGendrisch, F., Voelkel, L., Fluck, M., Apostolova, P., Zeiser, R., Jakob, T., Martin, S., & Esser, P. (2022). IRE1 and PERK signaling regulates inflammatory responses in a murine model of contact hypersensitivity. Allergy. 77(3), 966-978. https://doi.org/10.1111/all.15024



Schlagwörter

  
Go to first page
  
Go to previous page
  
1 von 2
  
Go to next page
  
Go to last page
  


Zuletzt aktualisiert 2025-21-05 um 18:19