Ana Martin-Villalba and her research team at the German Cancer Research Center followed stem cells along the path to neurons. The scientists analyzed at every step which genes were switched on and which of them were actually turned into new proteins. They expected to find that stem cells would simply switch their stem cell genes entirely off in order to become a neuron. But things turned out to be much more complicated. Martin-Villalba and her co-workers found that stem cell genes were not switched off, but simply put on standby, by preventing them from making the protein product that keeps the cell multipotent.
"To go into this standby mode and thus start the journey to become a neuron, stem cells switch off their inner signal to proliferate (called TOR) and stop to divide," says Ana Martin-Villalba. Very surprisingly, the researchers also found that stem cells always buy a return ticket. Just as flights can travel back and forth between countries, switching on or off TOR allows cells to travel from stem cell to neuron or back. "Thus, the decisions of a stem cell to become a neuron, remains reversible for some time," says Avni Baser, the scientist leading this project.
Normally, the travel of stem cells is in one direction to make nerve cells, unless something goes wrong in between. But if stem cells cannot properly control their TOR signal, they keep going back to stem cells, which in the long run can cause brain cancer rather than healing the brain. Indeed, in many cancers the levels of the TOR signal is artificially high. For future developments of stem cell therapy, understanding and controlling TOR activity in stem cell will thus be very important.
This article has been republished from materials provided by the German Cancer Research Center. Note: material may have been edited for length and content. For further information, please contact the cited source.
Baser, A., Skabkin, M., Kleber, S., Dang, Y., Balta, G. S., Kalamakis, G., . . . Martin-Villalba, A. (2019). Onset of differentiation is post-transcriptionally controlled in adult neural stem cells. Nature. doi:10.1038/s41586-019-0888-x