Mechanotransduction via the Piezo1-Akt pathway underlies Sost suppression in osteocytes

Biochem Biophys Res Commun. 2020 Jan 15;521(3):806-813. doi: 10.1016/j.bbrc.2019.10.174. Epub 2019 Nov 8.


Osteocytes function as critical regulators of bone homeostasis by coordinating the functions of osteoblasts and osteoclasts, and are constantly exposed to mechanical force. However, the molecular mechanism underlying the mechanical signal transduction in osteocytes is not well understood. Here, we found that Yoda1, a selective Piezo1 agonist, increased intracellular calcium mobilization and dose-dependently decreased the expression of Sost (encoding Sclerostin) in the osteocytic cell line IDG-SW3. We also demonstrated that mechanical stretch of IDG-SW3 suppressed Sost expression, a result which was abrogated by treatment with the Piezo1 inhibitor GsMTx4, and the deficiency of Piezo1. Furthermore, the suppression of Sost expression was abolished by treatment with an Akt inhibitor. Taken together, these results indicate that the activation of the Piezo1-Akt pathway in osteocytes is required for mechanical stretch-induced downregulation of Sost expression.

Keywords: Bone homeostasis; Calcium mobilization; Mechanical signal transduction; Mechanical stimulation; Mechanosensitive ion channel.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / genetics*
  • Animals
  • Down-Regulation
  • Ion Channels / metabolism*
  • Mechanotransduction, Cellular*
  • Mice
  • Osteocytes / cytology*
  • Osteocytes / metabolism
  • Proto-Oncogene Proteins c-akt / metabolism*
  • Signal Transduction


  • Adaptor Proteins, Signal Transducing
  • Ion Channels
  • Piezo1 protein, mouse
  • Sost protein, mouse
  • Proto-Oncogene Proteins c-akt