The scientists working at Johns Hopkins University located the control switches not at the gene level, but farther down the protein production line in more recently discovered forms of ribonucleic acid, or RNA. “Stem cells are poised to make proteins essential for maturing into blood cells, but microRNAs keep them locked in their place,” says cancer researcher Curt Civin, M.D., Ph.D., who led the study. Together with Robert Georgantas, Ph.D., research associate at the Johns Hopkins Kimmel Cancer Center, he sifted through thousands of RNA pieces with a custom-built, computer software program. Its algorithms let the software, fed data from samples of blood and bone marrow from healthy donors, match RNA pairs. The outcome was a core set of 33 microRNAs that match with more than 1,200 of the larger variety RNA already known to be important for stem-cell maturation.
Georgantas and Civin currently are testing whether these pair predictions are valid by using a non-reproducing virus to insert genetic instructions for each of the 33 microRNAs into adult stem cells. They’ll then be cultured in Petri dishes. MicroRNA-155 - the first microRNA tested - was predicted to stop stem cells from developing into red and white blood cells. As expected, stem cells without microRNA-155 matured: they formed approximately 75 red and 150 white blood cell colonies per dish. Stem cells with microRNA-155 matured into far fewer red and white cell colonies - about seven and 30 per dish, respectively.
“Using microRNAs to stall an adult blood stem cell in its early stage could help us grow new ones in test tubes, and perhaps give us more insight into stem-cell maturation for other tissue types,” says Civin.
MEDICA.de; Source: Johns Hopkins Medical Institutions