This technology describes a method for synchronizing the cell cycle in a population of stem cells to ensure a uniform response to differentiation signals.
Stem cells derived from patients can be differentiated into a variety of cell types, holding great potential for use in regenerative and personalized medicine. The large cell numbers needed for these applications, however, requires the expansion of cell populations in a 2D cell culture system, a process that often introduces asynchrony in cell cycle progression. This asynchrony greatly hinders the efficacy with which stem cells can be differentiated into target cell types, as cells may respond variably to exogenous factors. As such, there is a need for a simple culturing method that synchronizes the cell cycle in a population to enable a homogenous response to differentiation signals.
This technology is a drug-free method for synchronizing the cell cycles in a population of cells that only requires physical cell culture methods. Following suspension culture in methylcellulose, previously asynchronous cells are arrested at G1, a critical inflection point in the cell cycle. Subsequent 2D culture of arrested cells allows for simultaneous reentry to the cell cycle. The synchronized cell population can then be transferred to a 2D or 3D culture environment for optimal differentiation into the desired cell type. By ensuring all the cells in a population have a synchronized cell cycle, this technology provides a robust method for the generation of stem cells that could aid efforts in developing stem cell-based approaches to tissue engineering and regenerative medicine.
This technology has been validated in human and bovine stem cell populations from articular cartilage.
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holding great potential
critical inflection point
subsequent 2d culture
3d culture environment
asynchrony greatly hinders