Abnormal basement membrane results in increased keratinocyte‑derived periostin expression in psoriasis similar to wound healing

Flink, Lili Borbála and Gharrafinia, Ameneh and Papp, Benjamin Tamás and Varga, Ákos and Vigh, András István and Vidács, Dániel László and Kui, Róbert and Kemény, Lajos and Bata-Csörgő, Zsuzsanna and Bozó, Renáta (2023) Abnormal basement membrane results in increased keratinocyte‑derived periostin expression in psoriasis similar to wound healing. SCIENTIFIC REPORTS, 13. No. 16386. ISSN 2045-2322

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Abstract

The psoriatic skin resembles wound healing, and it shows abnormalities at the basement membrane (BM), also in the non-lesional skin. Fibroblast-derived dermal periostin has well-known functions in wound healing and Th2-mediated diseases, such as atopic dermatitis. Here we show that serum periostin level was elevated in psoriatic patients, remarkably in the systemically treated ones. Obvious periostin positivity was detected in basal keratinocytes of the non-lesional, lesional, and previouslylesional psoriatic vs. healthy skin. Ex vivo skin models were generated to examine how diferent skin injuries afect periostin expression during wound healing. Our newly developed cultured salt-split model demonstrated that BM-injury induced periostin expression in basal keratinocytes, and periostin levels in the supernatant were also increased upon healing. In wound healing models, β1-integrin expression was similarly induced. β1-integrin blocking caused reduced periostin expression in in vitro scratch assay, indicating that β1-integrin can mediate periostin production. In contrast to atopic dermatitis, psoriatic basal keratinocytes are in an activated state and show a stable wound healinglike phenotype with the overexpression of periostin. This abnormal BM-induced wound healing as a potential compensatory mechanism can be initiated already in the non-lesional skin present in the lesion and keratinocytes can remain activated in the healed skin.

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