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Development of brain stem cells into new nerve cells and why this can lead to cancer

Date:
January 31, 2019
Source:
German Cancer Research Center (Deutsches Krebsforschungszentrum, DKFZ)
Summary:
Stem cells are true Jacks-of-all-trades of our bodies, as they can turn into the many different cell types of all organs. This allows the tissues to renew and to heal after injury. This amazing multipotency makes stem cells in the adult body key tools for regenerative medicine. Scientists now report how brain stem cells make the decision to transform into new nerve cells.
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Stem cells are true Jacks-of-all-trades of our bodies, as they can turn into the many different cell types of all organs. This allows the tissues such as muscle or even brain to renew and to heal after injury. This amazing multipotency makes stem cells in the adult body key tools for the future of regenerative medicine. Scientists at the German Cancer Research Center (DKFZ) now publish in the journal Nature how brain stem cells make the decision to transform into new nerve cells.

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 where 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.


Story Source:

Materials provided by German Cancer Research Center (Deutsches Krebsforschungszentrum, DKFZ). Note: Content may be edited for style and length.


Journal Reference:

  1. Avni Baser, Maxim Skabkin, Susanne Kleber, Yonglong Dang, Gülce S. Gülcüler Balta, Georgios Kalamakis, Manuel Göpferich, Damian Carvajal Ibañez, Roman Schefzik, Alejandro Santos Lopez, Enric Llorens Bobadilla, Carsten Schultz, Bernd Fischer, Ana Martin-Villalba. Onset of differentiation is post-transcriptionally controlled in adult neural stem cells. Nature, 2019; DOI: 10.1038/s41586-019-0888-x

Cite This Page:

German Cancer Research Center (Deutsches Krebsforschungszentrum, DKFZ). "Development of brain stem cells into new nerve cells and why this can lead to cancer." ScienceDaily. ScienceDaily, 31 January 2019. <www.sciencedaily.com/releases/2019/01/190131143349.htm>.
German Cancer Research Center (Deutsches Krebsforschungszentrum, DKFZ). (2019, January 31). Development of brain stem cells into new nerve cells and why this can lead to cancer. ScienceDaily. Retrieved December 25, 2024 from www.sciencedaily.com/releases/2019/01/190131143349.htm
German Cancer Research Center (Deutsches Krebsforschungszentrum, DKFZ). "Development of brain stem cells into new nerve cells and why this can lead to cancer." ScienceDaily. www.sciencedaily.com/releases/2019/01/190131143349.htm (accessed December 25, 2024).

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