TY - JOUR
T1 - Cord blood-derived neuronal cells by ectopic expression of Sox2 and c-Myc
AU - Giorgetti, Alessandra
AU - Marchetto, Maria
AU - Li, Mo
AU - Yu, Diana
AU - Fazzina, Raffaella
AU - Mu, Yangling
AU - Adamo, Antonio
AU - Paramonov, Ida
AU - Cardoso, Julio
AU - Monasterio, Montserrat
AU - Bardy, Cedric
AU - Cassiani-Ingoni, Riccardo
AU - Liu, Guang
AU - Gage, Fred
AU - Belmonte, Juan
PY - 2012/7/31
Y1 - 2012/7/31
N2 - The finding that certain somatic cells can be directly converted into cells of other lineages by the delivery of specific sets of transcription factors paves the way to novel therapeutic applications. Here we show that human cord blood (CB) CD133+ cells lose their hematopoietic signature and are converted into CB-induced neuronal- like cells (CB-iNCs) by the ectopic expression of the transcription factor Sox2, a process that is further augmented by the combination of Sox2 and c-Myc. Gene-expression analysis, immunophenotyping, and electrophysiological analysis show that CB-iNCs acquire a distinct neuronal phenotype characterized by the expression of multiple neuronal markers. CB-iNCs show the ability to fire action potentials after in vitro maturation as well as after in vivo transplantation into the mouse hippocampus. This system highlights the potential of CB cells and offers an alternative means to the study of cellular plasticity, possibly in the context of drug screening research and of future cell-replacement therapies.
AB - The finding that certain somatic cells can be directly converted into cells of other lineages by the delivery of specific sets of transcription factors paves the way to novel therapeutic applications. Here we show that human cord blood (CB) CD133+ cells lose their hematopoietic signature and are converted into CB-induced neuronal- like cells (CB-iNCs) by the ectopic expression of the transcription factor Sox2, a process that is further augmented by the combination of Sox2 and c-Myc. Gene-expression analysis, immunophenotyping, and electrophysiological analysis show that CB-iNCs acquire a distinct neuronal phenotype characterized by the expression of multiple neuronal markers. CB-iNCs show the ability to fire action potentials after in vitro maturation as well as after in vivo transplantation into the mouse hippocampus. This system highlights the potential of CB cells and offers an alternative means to the study of cellular plasticity, possibly in the context of drug screening research and of future cell-replacement therapies.
KW - Neurons
KW - Reprogramming
KW - Stem cells
UR - http://www.scopus.com/inward/record.url?scp=84864527751&partnerID=8YFLogxK
U2 - 10.1073/pnas.1209523109
DO - 10.1073/pnas.1209523109
M3 - Article
SN - 0027-8424
VL - 109
SP - 12556
EP - 12561
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 31
ER -