| Autor: |
Wang NB; Department of Chemical Engineering, MIT, Cambridge, MA 02139, USA., Lende-Dorn BA; Department of Chemical Engineering, MIT, Cambridge, MA 02139, USA., Adewumi HO; Department of Biomedical Engineering, Boston University, Boston, MA 02215, USA., Beitz AM; Department of Chemical Engineering, MIT, Cambridge, MA 02139, USA., Han P; Department of Chemical Engineering, MIT, Cambridge, MA 02139, USA., O'Shea TM; Department of Biomedical Engineering, Boston University, Boston, MA 02215, USA., Galloway KE; Department of Chemical Engineering, MIT, Cambridge, MA 02139, USA. |
| Abstrakt: |
The sparse and stochastic nature of reprogramming has obscured our understanding of how transcription factors drive cells to new identities. To overcome this limit, we developed a compact, portable reprogramming system that increases direct conversion of fibroblasts to motor neurons by two orders of magnitude. We show that subpopulations with different reprogramming potentials are distinguishable by proliferation history. By controlling for proliferation history and titrating each transcription factor, we find that conversion correlates with levels of the pioneer transcription factor Ngn2, whereas conversion shows a biphasic response to Lhx3. Increasing the proliferation rate of adult human fibroblasts generates morphologically mature, induced motor neurons at high rates. Using compact, optimized, polycistronic cassettes, we generate motor neurons that graft with the murine central nervous system, demonstrating the potential for in vivo therapies. |
