Abstract
The simultaneous determination of the cell cycle phase of individual adherent mesenchymal stem cells (MSCs) using a fluorescence microscope after staining with 4',6-diamidine-2'-phenylindole dihydrochloride and bromodeoxyuridine and the laser phase shift by phase-shifting laser microscopy (PLM) revealed that the laser phase shift of cells in the G(2)/M phase was markedly higher than that of cells in the G(0)/G(1) phase. Even in the synchronous cultures to G(0)/G(1) and G(2)/M cell cycle phases, the laser phase shift of the cells in the G(2)/M phase was markedly higher than that of the cells in the G(0)/G(1) phase. The analysis of the cultures of MSCs from different donors with the addition of FGF2 at different concentrations revealed that there was a marked negative correlation between the average phase shift and mean generation time. In conclusion, it is possible to estimate noninvasively the proliferation activity of MSCs population by measuring the phase shift using PLM.
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