摘要：SummaryPreadipocyte differentiation can be induced upon a hormonal treatment, and various factors secreted by the cells may contribute to adipogenesis. In this study, RNA-seq revealed Serpina3c as a critical factor regulating the signaling network during adipogenesis. Serpina3c is a secretory protein and is highly expressed in fat tissues. Knockdown of Serpina3c decreased adipogenesis by attenuating the mitotic clonal expansion of 3T3-L1 cells. These cells exhibited decreases in integrin α5, which abolished the phosphorylation of integrin β3. We found that Serpina3c inhibits a serine protease that regulates integrin α5 degradation. Knockdown of Serpina3c disrupted integrin-mediated insulin growth factor 1 (IGF-1) signaling and ERK activation. Serpina3c-mediated regulation of integrin-IGF-1 signaling is also associated with AKT activation, which affects the nuclear translocation of GSK3β. Altogether, our results indicate that Serpina3c secreted from differentiating adipocytes inhibits serine proteases to modulate integrin/IGF-1-mediated ERK and AKT signaling and thus is a critical factor contributing to adipogenesis.Graphical AbstractDisplay OmittedHighlights•RNA-seq revealed Serpina3c as a critical factor regulating adipogenesis•Knockdown of Serpina3c attenuated the mitotic clonal expansion of 3T3-L1 cells•Knockdown of Serpina3c leads to the degradation of integrin α5•Serpina3c regulates integrin-mediated IGF-1 signaling and ERK/AKT activationMolecular Biology; Developmental Biology; Transcriptomics
