The Molecular Signature Related to Local Inflammatory and Immune Response in Canine Cutaneous Hypersensitivity Reactions: A Preliminary Study.
Camilla CapacciaFrancesco CiancabillaIlaria PorcellatoChiara BrachelenteMassimo ZeraniMargherita MaranesiGabriella GuelfiPublished in: Current issues in molecular biology (2024)
Cutaneous hypersensitivity reactions (CHRs) are complex inflammatory skin disorders that affect humans and dogs. This study examined the inflammatory and immune responses leading to skin damage, inflammation, and irritation by investigating gene expression through quantitative PCR (qPCR) and protein localization through the immunohistochemistry (IHC) of specific receptors and molecules involved in CHRs. Formalin-fixed paraffin-embedded (FFPE) samples from canine CHR skin (n = 20) and healthy dog skin (n = 3) were analyzed for expression levels of eight genes, including members of the pattern recognition receptor (PRR) family, CD209 and CLEC4G, the Regakine-1-like chemokine, and acute phase proteins (APPs), LBP-like and Hp-like genes. Additionally, we examined the local involvement of IL-6, Janus Kinase 1 (JAK1), and the signal transducer activator of transcription 3 (STAT3) in the CHR cases. The study demonstrated statistically significant increases in the expression levels of CD209, Hp-like ( p < 0.01), LBP-like, Regakine-1-like, and CLEC4G ( p < 0.05) genes in CHRs compared to healthy controls. Conversely, IL-6, JAK1, and STAT3 showed no significant difference between the two groups ( p > 0.05). Protein analysis revealed JAK1 and STAT3 expression in CHR hyperplastic epithelial cells, dermal fibroblasts, and endothelial cells of small capillaries, indicating a possible involvement in the JAK/STAT pathway in local inflammatory response regulation. Our findings suggest that the skin plays a role in the development of CHRs.
Keyphrases
- immune response
- wound healing
- soft tissue
- poor prognosis
- oxidative stress
- gene expression
- inflammatory response
- binding protein
- endothelial cells
- genome wide
- cell proliferation
- dna methylation
- toll like receptor
- drug induced
- genome wide identification
- bioinformatics analysis
- transcription factor
- lipopolysaccharide induced
- single cell
- genome wide analysis