Serpina3c Regulates Adipogenesis by Modulating Insulin Growth Factor 1 and Integrin Signaling

• Main Authors: Yoonjeong Choi, Hyeonjin Choi, Bo Kyung Yoon, Hyemin Lee, Jo Woon Seok, Hyo Jung Kim, Jae-woo Kim
• Format: Article
• Language: English
• Published: Elsevier 2020-03-01
• Series: iScience
• Online Access: http://www.sciencedirect.com/science/article/pii/S2589004220301450

Summary: Preadipocyte 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. : Molecular Biology; Developmental Biology; Transcriptomics Subject Areas: Molecular Biology, Developmental Biology, Transcriptomics