[HTML][HTML] Transcription factor-mediated lineage switching reveals plasticity in primary committed progenitor cells

C Heyworth, S Pearson, G May, T Enver - The EMBO journal, 2002 - embopress.org
C Heyworth, S Pearson, G May, T Enver
The EMBO journal, 2002embopress.org
The developmental plasticity of transplanted adult stem cells challenges the notion that
tissue-restricted stem cells have stringently limited lineage potential and prompts a re-
evaluation of the stability of lineage commitment. Transformed cell systems are
inappropriate for such studies, since transformation potentially dysregulates the processes
governing lineage commitment. We have therefore assessed the stability of normal lineage
commitment in primary adult haematopoietic cells. For these studies we have used …
The developmental plasticity of transplanted adult stem cells challenges the notion that tissue-restricted stem cells have stringently limited lineage potential and prompts a re-evaluation of the stability of lineage commitment. Transformed cell systems are inappropriate for such studies, since transformation potentially dysregulates the processes governing lineage commitment. We have therefore assessed the stability of normal lineage commitment in primary adult haematopoietic cells. For these studies we have used prospectively isolated primary bipotent progenitors, which normally display only neutrophil and monocyte differentiation in vitro. In response to ectopic transcription factor expression, these neutrophil/monocyte progenitors were reprogrammed to take on erythroid, eosinophil and basophil-like cell fates, with the resultant colonies resembling the mixed lineage colonies normally generated by multipotential progenitors. Clone-marking and daughter cell experiments identified lineage switching rather than differential cell selection as the mechanism of altered lineage output. These results demonstrate that the cell type-specific programming of apparently committed primary progenitors is not irrevocably fixed, but may be radically re-specified in response to a single transcriptional regulator.
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