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High-throughput proteomic analysis of chronic inflammatory skin diseases: Psoriasis and atopic dermatitis.
Traks, Tanel; Reemann, Paula; Eskla, Kattri-Liis; Ottas, Aigar; Jagomäe, Toomas; Liira, Rasmus; Ilves, Liis; Jaks, Viljar; Raam, Liisi; Abram, Kristi; Kingo, Külli.
Afiliación
  • Traks T; Department of Dermatology and Venereology, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia.
  • Reemann P; Clinical Research Centre, Tartu University Hospital, University of Tartu, Tartu, Estonia.
  • Eskla KL; Department of Dermatology and Venereology, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia.
  • Ottas A; Department of Physiology, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia.
  • Jagomäe T; Clinical Research Centre, Tartu University Hospital, University of Tartu, Tartu, Estonia.
  • Liira R; Estonian Genome Centre, Institute of Genomics, University of Tartu, Tartu, Estonia.
  • Ilves L; Department of Physiology, Institute of Biomedicine and Translational Medicine, University of Tartu, Tartu, Estonia.
  • Jaks V; Institute of Physics, University of Tartu, Tartu, Estonia.
  • Raam L; Department of Dermatology and Venereology, Institute of Clinical Medicine, University of Tartu, Tartu, Estonia.
  • Abram K; Dermatology Clinic, Tartu University Hospital, Tartu, Estonia.
  • Kingo K; Dermatology Clinic, Tartu University Hospital, Tartu, Estonia.
Exp Dermatol ; 33(4): e15079, 2024 Apr.
Article en En | MEDLINE | ID: mdl-38654506
ABSTRACT
Common characteristics in the pathogenesis of psoriasis (PS) and atopic dermatitis (AD) have been presumed, but only a few studies have clearly supported this. The current aim was to find possible similarities and differences in protein expression patterns between these two major chronic inflammatory skin diseases. High-throughput tandem mass spectrometry proteomic analysis was performed using full thickness skin samples from adult PS patients, AD patients and healthy subjects. We detected a combined total of 3045 proteins in the three study groups. According to principal component analysis, there was significant overlap between the proteomic profiles of PS and AD, and both clearly differed from that of healthy skin. The following validation of selected proteins with western blot analysis showed similar tendencies in expression levels and produced statistically significant results. The expression of periostin (POSTN) was consistently high in AD and very low or undetectable in PS (5% FDR corrected p < 0.001), suggesting POSTN as a potential biomarker to distinguish these diseases. Immunohistochemistry further confirmed higher POSTN expression in AD compared to PS skin. Overall, our findings support the concept that these two chronic skin diseases might share considerably more common mechanisms in pathogenesis than has been suspected thus far.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Psoriasis / Moléculas de Adhesión Celular / Proteómica / Dermatitis Atópica Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Exp Dermatol Asunto de la revista: DERMATOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Estonia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Psoriasis / Moléculas de Adhesión Celular / Proteómica / Dermatitis Atópica Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Exp Dermatol Asunto de la revista: DERMATOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Estonia