MiR‐494‐3p regulates skin fibroblast activities by mediating fibromodulin production

Abstract Skin wound healing is a well‐coordinated process in which various cells and factors participate, during which fibroblast exhibits a critical role by exerting its multiple activities, including proliferation, migration, invasion, and differentiation. Previous studies have identified that fibromodulin (FMOD) could enhance dermal wound healing by promoting skin fibroblast activities, but little is known about its upstream regulator. We occasionally found that FMOD expression was downregulated in skin fibroblast by transforming growth factor‐β1 treatment. It was hypothesized that microRNAs (miRNA) in skin fibroblast could downregulate FMOD production and blocking them would increase FMOD expression, as well as promote skin wound healing. Here, by utilizing combined analysis of miRNA microarray from the Gene Expression Omnibus database and miRNA targets prediction, we successfully identified a miRNA, termed miR‐494‐3p, could regulate FMOD production in human skin fibroblast (BJ fibroblast). The functional analysis revealed that miR‐494‐3p mimics could inhibit BJ fibroblast migration and invasion but not proliferation and differentiation, while miR‐494‐3p inhibition markedly promotes migration, invasion, and differentiation of BJ fibroblast. Moreover, we established FMOD overexpression (OE) and knockout BJ fibroblast. We found that FMOD OE could rescue the inhibitory effects of miR‐494‐3p mimics on the migration and invasion of BJ fibroblast. In contrast, the miR‐494‐3p inhibitor transfection could not enhance migration, invasion, and differentiation of FMOD KO BJ fibroblast. Together, our results suggest that miR‐494‐3p may be a potential target for skin wound management via regulating FMOD production.