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Immunolocalization and Expression of JAK1 and JAK3 in the Skin of Dust Mite-Sensitive Beagle Dogs before and after Allergen Exposure

SIMPLE SUMMARY: Our study aimed to stain a cellular pathway that is a potential target of drugs to treat allergies. In our study, we took skin samples from dogs allergic to dust, before and after exposure to dust mites, and stained those samples for this pathway. We found that this pathway was prese...

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Detalles Bibliográficos
Autores principales: Sartori, Roberta, Ahrens, Kim, Wilkes, Rachel, Marsella, Rosanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10458269/
https://www.ncbi.nlm.nih.gov/pubmed/37624299
http://dx.doi.org/10.3390/vetsci10080512
Descripción
Sumario:SIMPLE SUMMARY: Our study aimed to stain a cellular pathway that is a potential target of drugs to treat allergies. In our study, we took skin samples from dogs allergic to dust, before and after exposure to dust mites, and stained those samples for this pathway. We found that this pathway was present in skin cells and that exposure to the dust mites changed how this pathway was expressed. These results confirm that this pathway plays a role in the course of allergic responses and that topical creams targeting this pathway can be promising to treat allergic skin disease. ABSTRACT: Janus kinase (JAK) pathways have emerged as targets of treatment, yet localization and expression of JAK1 and JAK3 in canine atopic skin have not been studied. This study aimed to compare the localization and expression of JAK1 and JAK3 in the skin of atopic dogs before and after allergen exposure. Skin biopsies taken from atopic beagles sensitized to house dust mites (HDM) before (D0) and after four weeks (D28) of allergen exposure were stained. Staining was subjectively scored by examiners unaware of the source of the slides. Image J was used for the semiquantitative assessment of staining intensity. JAK1 and JAK3 staining was epidermal and dermal. JAK1 staining was cytoplasmic, primarily found in basal keratinocytes and dermal cells, while JAK 3 was nuclear (all epidermal levels and on dermal inflammatory cells). Epidermal thickness was significantly higher on D28 than on D0 (p < 0.0001). For JAK1, epidermal staining divided by epithelial thickness was significantly lower on D28 (p = 0.0002) compared to D0. For JAK3 staining, intensity in the dermis was significantly higher on D28 (p = 0.0405) compared to D0. We conclude that decreased expression of JAK1 in the epidermis and increased expression of JAK3 in the dermis of atopic dogs occur after allergen exposure.