Background: Psoriasis is a chronic inflammatory skin disease. The etiology of psoriasis is not fully understood, but the genetic background is considered to be the most important factor. To date, many psoriasis-related genes have been discovered, but the role of many important genes has not been well understood.
Objective: The purpose of this study is to uncover possible roles of in psoriasis.
Methods: Expression of MDA5 was investigated using immunohistochemistry. Then, was overexpressed in keratinocytes using a recombinant adenovirus.
Results: As a result of immunohistochemical staining, the expression of was significantly increased in the epidermis of psoriasis compared to normal skin. Similarly, the expression of was increased in imiquimod-induced psoriasiform dermatitis model. In cultured keratinocytes, toll-like receptor 3 agonist poly(I:C) induced expression of at both mRNA and protein levels. When was overexpressed using a recombinant adenovirus, poly(I:C)-induced cytokine expression was significantly increased. Finally, overexpression significantly inhibited calcium-induced differentiation of keratinocytes.
Conclusion: These results suggest that MDA5 increases in psoriasis and negatively regulates keratinocyte differentiation.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8273324 | PMC |
http://dx.doi.org/10.5021/ad.2021.33.4.339 | DOI Listing |
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