YAP1 influences differentiation of osteoblastic MC3T3‐E1 cells through the regulation of ID1. Issue 8 (7th January 2019) - Yang, Beining
Abstract: Yes‐associated protein 1 (YAP1) transcriptional coactivator has recently been identified to regulate skeletal lineage cell differentiation and bone development. However, the role and molecular mechanisms of YAP1 in the regulation of osteoblastic differentiation remains to be elucidated. In this study, we demonstrated that YAP1 expression was increased during osteogenic differentiation of rat bone mesenchymal stem cells and MC3T3‐E1. YAP1 overexpression MC3T3‐E1 showed increased expression of osteogenesis markers, such as runt‐related transcription factor 2, osteocalcin, and osteopontin, as well as alkaline phosphatase and alizarin red staining. Conversely, YAP1 knockdown significantly suppressed MC3T3‐E1 osteoblastic differentiation. Mechanistically, we found that YAP1 overexpression upregulated the mRNA and protein expression of the inhibitor of differentiation/DNA binding 1 (ID1), which was contrary to the results of YAP1‐knockdown group. Moreover, the early osteogenic differentiation of MC3T3‐E1 cells was enhanced by ID1 overexpression. Furthermore, transient transfection with exogenous ID1 overexpression plasmid completely recaptured the decreased effects of YAP1 knockdown on MC3T3‐E1 cell differentiation. In addition, β‐catenin and AMP‐activated protein kinase signaling pathways participated in YAP1 regulation processes. Taken together, our study suggests that YAP1 is a crucial modulator of osteoblast differentiation in vitro, and provides insight into the mechanism by which YAP1 regulates osteoblast differentiation. Abstract : Schematic diagram depicting the role and mechanisms of Yes‐associated protein 1 (YAP1) in the differentiation of MC3T3‐E1. YAP1 plays a positive role in the osteogenic differentiation of MC3T3‐E1, partly through the regulation of ID1. Meanwhile, YAP1 activated β‐catenin and inhibited AMP‐activated protein kinase signaling pathways.