BK Channel Deficiency in Osteoblasts Reduces Bone Formation via the Wnt/β-Catenin Pathway

Mol Cells. 2021 Aug 31;44(8):557-568. doi: 10.14348/molcells.2021.0004.

Abstract

Global knockout of the BK channel has been proven to affect bone formation; however, whether it directly affects osteoblast differentiation and the mechanism are elusive. In the current study, we further investigated the role of BK channels in bone development and explored whether BK channels impacted the differentiation and proliferation of osteoblasts via the canonical Wnt signaling pathway. Our findings demonstrated that knockout of Kcnma1 disrupted the osteogenesis of osteoblasts and inhibited the stabilization of β-catenin. Western blot analysis showed that the protein levels of Axin1 and USP7 increased when Kcnma1 was deficient. Together, this study confirmed that BK ablation decreased bone mass via the Wnt/β-catenin signaling pathway. Our findings also showed that USP7 might have the ability to stabilize the activity of Axin1, which would increase the degradation of β-catenin in osteoblasts.

Keywords: BK channel; Kcnma1; bone development; osteoblasts; β-catenin.

MeSH terms

  • Animals
  • Cell Differentiation
  • Female
  • Gene Deletion
  • Large-Conductance Calcium-Activated Potassium Channels / deficiency*
  • Large-Conductance Calcium-Activated Potassium Channels / metabolism
  • Mice
  • Mice, Knockout
  • Osteoblasts / metabolism*
  • Osteogenesis*
  • Wnt Signaling Pathway*
  • beta Catenin / metabolism

Substances

  • Large-Conductance Calcium-Activated Potassium Channels
  • beta Catenin