2 min readBiology Behind Stem Cells Could Improve Systems to Deliver Treatments or Cells for Tissue Repair
Hinxton, UK – New cells used in growth or for repair of a damaged tissue derive from a group of specialized dividing cells – stem cells. Stem cells can divide to maintain the source of new cells or can commit irrevocably to becoming a specialized cell, such as a liver or pancreas cell.
Now, researchers describe the switches that determine how stem cells make that crucial decision. Their work might enable stem cells to be converted into a range of adult tissues more efficiently and more homogeneously.
Pluripotent stem cells have the potential to become any cell in the body. Interest in them has grown with the hope that they might be used to replace dying or damaged cells with healthy cells. Repairing tissues would be important in organ regeneration, bone repair and treatment of neurodegenerative diseases.
The team looked at the activity of key genes and proteins during the cell cycle – the processes by which a cell divides – in human pluripotent stem cells. They found that the molecular decision to continue to divide or to differentiate – to commit to a pathway towards a defined tissue type – is made during a restricted phase of the cell cycle.
“We know that cell division and differentiation need to be interconnected, but the mechanisms involved are yet to be uncovered,” says Dr. Ludovic Vallier, lead author from the Wellcome Trust Sanger Institute and the University of Cambridge. “For the first time, we have a glimpse of how these two processes are biologically linked.”
“We have found key regulators of this process and have new methods that could more efficiently produce cell types with a clinical interest from human pluripotent stem cells.”
They looked at the times during the cell cycle that the stem cell could commit to specific lineages, including liver and pancreas. They found that the decision could be made only at certain stages of the cell cycle and that the timing of the decision could drive the cell down different pathways.
This potential synchronization of stem cells could result in new methods to generate specific cell types for regenerative medicine.
The team showed that these cell-cycle restricted decisions are influenced by a group of proteins known as cyclin Ds. The activity of these proteins, which control cell cycle progression, only direct the differentiation of human embroyonic stem cells toward specific lineages by controlling external stimuli. It is possible that the cyclin D mechanisms the team found in human stem cells work in a similar way during the development of human organs and in the natural repair or regrowth of tissues in adults.
The researchers also found that they could use a simple chemical compound, rather than a protein, to drive the stem cells towards tissues such as the liver. Modifying the activity of cell cycle regulators with simpler chemical treatments could make stem cell differentiation more efficient in the future.
Publication: The cell-cycle state of stem cells determines cell fate propensity. Pauklin S, Vallier L. Cell (2013): http://www.cell.com/retrieve/pii/S0092867413010258