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Direct conversion of fibroblasts to functional neurons by defined factors.

Nature | 2010

Cellular differentiation and lineage commitment are considered to be robust and irreversible processes during development. Recent work has shown that mouse and human fibroblasts can be reprogrammed to a pluripotent state with a combination of four transcription factors. This raised the question of whether transcription factors could directly induce other defined somatic cell fates, and not only an undifferentiated state. We hypothesized that combinatorial expression of neural-lineage-specific transcription factors could directly convert fibroblasts into neurons. Starting from a pool of nineteen candidate genes, we identified a combination of only three factors, Ascl1, Brn2 (also called Pou3f2) and Myt1l, that suffice to rapidly and efficiently convert mouse embryonic and postnatal fibroblasts into functional neurons in vitro. These induced neuronal (iN) cells express multiple neuron-specific proteins, generate action potentials and form functional synapses. Generation of iN cells from non-neural lineages could have important implications for studies of neural development, neurological disease modelling and regenerative medicine.

Pubmed ID: 20107439 RIS Download

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Associated grants

  • Agency: NCI NIH HHS, United States
    Id: T32 CA009302
  • Agency: NHLBI NIH HHS, United States
    Id: U01 HL100397
  • Agency: PHS HHS, United States
    Id: 1018438-142-PABCA
  • Agency: NINDS NIH HHS, United States
    Id: T32 NS007280
  • Agency: NINDS NIH HHS, United States
    Id: 5T32NS007280
  • Agency: Howard Hughes Medical Institute, United States

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C57BL/6J (tool)

RRID:IMSR_JAX:000664

Mus musculus with name C57BL/6J from IMSR.

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Olig1 (antibody)

RRID:AB_10674111

This monoclonal targets Olig1

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