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Pflugers Arch ; 461(1): 191-202, 2011 Jan.
Article in English | MEDLINE | ID: mdl-21110038

ABSTRACT

Embryonic stem cells (ESCs) can uniquely proliferate indefinitely and differentiate into all cell lineages. ESCs may therefore provide an unlimited supply of cells for cell-based therapies. Previous study reported the presence of hyperpolarization-activated inward currents in undifferentiated mouse (m) ESCs, but the functional role of this hyperpolarization-activated current in mESCs is unknown. In this study, the role of this current in maintaining the proliferative capacity and the cell cycle progression of ESCs was investigated. In D3 mESCs, this hyperpolarization-activated inward current can be blocked by HCN channel blocker ZD7288. Application of the HCN channel blockers, cesium (1-10 mM) or ZD7288 (0.1-30 µM), attenuated cell proliferation in a concentration-dependent manner. Both HCN blockers were found to be non-cytotoxic to mESCs as determined by cell viability test. Interestingly, ZD7288 at 10 and 30 µM was found to decrease the proportion of cells in G(0)/G(1) phase and increase the proportion of cells in S phase. This suggests that this hyperpolarization-activated current can affect the cell cycle progression in mESCs. In summary, the present investigation suggests that ESC proliferation and cell cycle progression can be regulated by this hyperpolarization-activated current.


Subject(s)
Cell Cycle/drug effects , Cell Proliferation/drug effects , Cyclic Nucleotide-Gated Cation Channels/antagonists & inhibitors , Embryonic Stem Cells/cytology , Animals , Cell Survival/drug effects , Cesium/pharmacology , Cyclic Nucleotide-Gated Cation Channels/metabolism , Cyclin B/biosynthesis , Embryonic Stem Cells/drug effects , Hyperpolarization-Activated Cyclic Nucleotide-Gated Channels , Membrane Potentials , Mice , Patch-Clamp Techniques , Pyrimidines/pharmacology
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