Protease-Activated Receptor-2 Regulates Neuro-Epidermal Communication in Atopic Dermatitis - Université Paris Cité Access content directly
Journal Articles Frontiers in Immunology Year : 2020

Protease-Activated Receptor-2 Regulates Neuro-Epidermal Communication in Atopic Dermatitis

Timo Buhl
  • Function : Author
Akihiko Ikoma
  • Function : Author
Cordula Kempkes
  • Function : Author
Ferda Cevikbas
  • Function : Author
Mathias Sulk
  • Function : Author
Joerg Buddenkotte
  • Function : Author
Tasuku Akiyama
  • Function : Author
Debbie Crumrine
  • Function : Author
Eric Camerer
Earl Carstens
  • Function : Author
Michael Schön
  • Function : Author
Peter Elias
  • Function : Author
Shaun Coughlin
  • Function : Author
Martin Steinhoff
  • Function : Author


Background: Activation of protease-activated receptor-2 (PAR2) has been implicated in inflammation, pruritus, and skin barrier regulation, all characteristics of atopic dermatitis (AD), as well as Netherton syndrome which has similar characteristics. However, understanding the precise role of PAR2 on neuro-immune communication in AD has been hampered by the lack of appropriate animal models. Methods: We used a recently established mouse model with epidermal overexpression of PAR2 (PAR2OE) and littermate WT mice to study the impact of increased PAR2 expression in epidermal cells on spontaneous and house dust mite (HDM)-induced skin inflammation, itch, and barrier dysfunction in AD, in vivo and ex vivo. Results: PAR2OE newborns displayed no overt abnormalities, but spontaneously developed dry skin, severe pruritus, and eczema. Dermatological, neurophysiological, and immunological analyses revealed the hallmarks of AD-like skin disease. Skin barrier defects were observed before onset of skin lesions. Application of HDM onto PAR2OE mice triggered pruritus and the skin phenotype. PAR2OE mice displayed an increased density of nerve fibers, increased nerve growth factor and endothelin-1 expression levels, alloknesis, enhanced scratching (hyperknesis), and responses of dorsal root ganglion cells to non-histaminergic pruritogens. Conclusion: PAR2 in keratinocytes, activated by exogenous and endogenous proteases, is sufficient to drive barrier dysfunction, inflammation, and pruritus and sensitize skin to the effects of HDM in a mouse model that mimics human AD. PAR2 signaling in keratinocytes appears to be sufficient to drive several levels of neuro-epidermal communication, another feature of human AD.



Dates and versions

hal-03906246 , version 1 (19-12-2022)



Timo Buhl, Akihiko Ikoma, Cordula Kempkes, Ferda Cevikbas, Mathias Sulk, et al.. Protease-Activated Receptor-2 Regulates Neuro-Epidermal Communication in Atopic Dermatitis. Frontiers in Immunology, 2020, 11, ⟨10.3389/fimmu.2020.01740⟩. ⟨hal-03906246⟩


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