| Autor: |
Chubinskiy-Nadezhdin VI; Institute of Cytology RAS, 194064, Tikhoretsky Ave. 4, St. Petersburg, Russia. vchubinskiy@gmail.com., Sudarikova AV; Institute of Cytology RAS, 194064, Tikhoretsky Ave. 4, St. Petersburg, Russia., Shilina MA; Institute of Cytology RAS, 194064, Tikhoretsky Ave. 4, St. Petersburg, Russia., Vasileva VY; Institute of Cytology RAS, 194064, Tikhoretsky Ave. 4, St. Petersburg, Russia., Grinchuk TM; Institute of Cytology RAS, 194064, Tikhoretsky Ave. 4, St. Petersburg, Russia., Lyublinskaya OG; Institute of Cytology RAS, 194064, Tikhoretsky Ave. 4, St. Petersburg, Russia., Nikolsky NN; Institute of Cytology RAS, 194064, Tikhoretsky Ave. 4, St. Petersburg, Russia., Negulyaev YA; Institute of Cytology RAS, 194064, Tikhoretsky Ave. 4, St. Petersburg, Russia.; Department of Medical Physics, Peter the Great St. Petersburg Polytechnic University, 29, Polytechnicheskaya st., 195251, St. Petersburg, Russia. |
| Abstrakt: |
The study of ion channels in stem cells provides important information about their role in stem cell fate. Previously we have identified the activity of calcium-activated potassium channels of big conductance (BK channels) in human endometrium-derived mesenchymal stem cells (eMSCs). BK channels could have significant impact into signaling processes by modulating membrane potential. The membrane potential and ionic permeability dynamically changes during cycle transitions. Here, we aimed at verification of the role of BK channels as potassium transporting pathway regulating cell cycle passageway of eMSCs. The functional expression of native BK channels was confirmed by patch-clamp and immunocytochemistry. In non-synchronized cells immunofluorescent analysis revealed BK-positive and BK-negative stained eMSCs. Using cell synchronization, we found that the presence of BK channels in plasma membrane was cell cycle-dependent and significantly decreased in G2M phase. However, the study of cell cycle progression in presence of selective BK channel inhibitors showed no effect of pore blockers on cycle transitions. Thus, BK channel-mediated K + transport is not critical for the fundamental mechanism of passageway through cell cycle of eMSCs. At the same time, the dynamics of the presence of BK channels on plasma membrane of eMSCs can be a novel indicator of cellular proliferation. |
