Fluid shear stress induces Runx‐2 expression via upregulation of PIEZO1 in MC3T3‐E1 cells

J Song, L Liu, L Lv, S Hu, A Tariq… - Cell biology …, 2020 - Wiley Online Library
J Song, L Liu, L Lv, S Hu, A Tariq, W Wang, X Dang
Cell biology international, 2020Wiley Online Library
Mechanically induced biological responses in bone cells involve a complex biophysical
process. Although various mechanosensors have been identified, the precise
mechanotransduction pathway remains poorly understood. PIEZO1 is a newly discovered
mechanically activated ion channel in bone cells. This study aimed to explore the
involvement of PIEZO1 in mechanical loading (fluid shear stress)‐induced signaling
cascades that control osteogenesis. The results showed that fluid shear stress increased …
Abstract
Mechanically induced biological responses in bone cells involve a complex biophysical process. Although various mechanosensors have been identified, the precise mechanotransduction pathway remains poorly understood. PIEZO1 is a newly discovered mechanically activated ion channel in bone cells. This study aimed to explore the involvement of PIEZO1 in mechanical loading (fluid shear stress)‐induced signaling cascades that control osteogenesis. The results showed that fluid shear stress increased PIEZO1 expression in MC3T3‐E1 cells. The fluid shear stress elicited the key osteoblastic gene Runx‐2 expression; however, PIEZO1 silencing using small interference RNA blocked these effects. The AKT/GSK‐3β/β‐catenin pathway was activated in this process. PIEZO1 silencing impaired mechanically induced activation of the AKT/GSK‐3β/β‐catenin pathway. Therefore, the results demonstrated that MC3T3‐E1 osteoblasts required PIEZO1 to adapt to the external mechanical fluid shear stress, thereby inducing osteoblastic Runx‐2 gene expression, partly through the AKT/GSK‐3β/β‐catenin pathway.
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