Projects per year
Abstract
Cell lineage reprogramming via transgene overexpression of key master regulatory transcription factors has been well-documented. However, the poor efficiency and lack of fidelity of this approach is problematic. Synthetic transcription factors (sTFs) – built from the repurposed CRISPR/Cas9
system – can activate endogenous target genes to direct differentiation or trigger lineage reprogramming. Here we explored whether sTFs could be used to steer mouse neural stem cells and mouse embryonic fibroblasts towards the oligodendrocyte lineage. We developed a non-viral modular expression system to enable stable multiplex delivery of pools of sTFs capable of transcriptional
activation of three key oligodendrocyte lineage master regulatory genes (Sox10, Olig2 and Nkx6-2). Delivery of these sTFs could enhance neural stem cell differentiation and initiated mouse embryonic fibroblast direct reprograming towards oligodendrocyte progenitor-like cells. Our findings demonstrate the value of sTFs as tools for activating endogenous genes and directing mammalian cell type identity.
system – can activate endogenous target genes to direct differentiation or trigger lineage reprogramming. Here we explored whether sTFs could be used to steer mouse neural stem cells and mouse embryonic fibroblasts towards the oligodendrocyte lineage. We developed a non-viral modular expression system to enable stable multiplex delivery of pools of sTFs capable of transcriptional
activation of three key oligodendrocyte lineage master regulatory genes (Sox10, Olig2 and Nkx6-2). Delivery of these sTFs could enhance neural stem cell differentiation and initiated mouse embryonic fibroblast direct reprograming towards oligodendrocyte progenitor-like cells. Our findings demonstrate the value of sTFs as tools for activating endogenous genes and directing mammalian cell type identity.
Original language | English |
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Journal | Stem Cell Reports |
DOIs | |
Publication status | Published - 7 Nov 2019 |
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Dive into the research topics of 'Reprogramming of Fibroblasts to Oligodendrocyte Progenitor-like Cells Using CRISPR/Cas9-Based Synthetic Transcription Factors'. Together they form a unique fingerprint.Projects
- 1 Finished
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SynthSys-Mammalian: Edinburgh Mammalian Synthetic Biology Research Centre
Pollard, S. (Principal Investigator) & Ffrench-Constant, C. (Co-investigator)
14/11/14 → 31/03/22
Project: Research
Profiles
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Steven Pollard
- Deanery of Clinical Sciences - Personal Chair of Stem Cell and Cancer Biology
- Centre for Regenerative Medicine
- Edinburgh Neuroscience
- Centre for Engineering Biology
Person: Academic: Research Active