Local calcium signalling is mediated by mechanosensitive ion channels in mesenchymal stem cells

Biochem Biophys Res Commun. 2017 Jan 22;482(4):563-568. doi: 10.1016/j.bbrc.2016.11.074. Epub 2016 Nov 14.

Abstract

Mechanical forces are implicated in key physiological processes in stem cells, including proliferation, differentiation and lineage switching. To date, there is an evident lack of understanding of how external mechanical cues are coupled with calcium signalling in stem cells. Mechanical reactions are of particular interest in adult mesenchymal stem cells because of their promising potential for use in tissue remodelling and clinical therapy. Here, single channel patch-clamp technique was employed to search for cation channels involved in mechanosensitivity in mesenchymal endometrial-derived stem cells (hMESCs). Functional expression of native mechanosensitive stretch-activated channels (SACs) and calcium-sensitive potassium channels of different conductances in hMESCs was shown. Single current analysis of stretch-induced channel activity revealed functional coupling of SACs and BK channels in plasma membrane. The combination of cell-attached and inside-out experiments have indicated that highly localized Ca2+ entry via SACs triggers BK channel activity. At the same time, SK channels are not coupled with SACs despite of high calcium sensitivity as compared to BK. Our data demonstrate novel mechanism controlling BK channel activity in native cells. We conclude that SACs and BK channels are clusterized in functional mechanosensitive domains in the plasma membrane of hMESCs. Co-clustering of ion channels may significantly contribute to mechano-dependent calcium signalling in stem cells.

Keywords: Calcium signalling; Mechanotransduction; Mesenchymal stem cells; Stretch-activated channels.

MeSH terms

  • Calcium / metabolism
  • Calcium Signaling*
  • Cells, Cultured
  • Endometrium / cytology
  • Female
  • Humans
  • Ion Channels / metabolism*
  • Mechanotransduction, Cellular*
  • Mesenchymal Stem Cells / cytology
  • Mesenchymal Stem Cells / metabolism*

Substances

  • Ion Channels
  • Calcium