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• W2800140873 abstract "Identification of optimal transcription factor expression patterns to direct cellular differentiation along a desired pathway presents significant challenges. We demonstrate massively combinatorial screening of temporally-varying mRNA transcription factors to direct differentiation of neural progenitor cells using a dynamically-reconfigurable magnetically-guided spotting technology for localizing mRNA, enabling experiments on millimetre size spots. In addition, we present a time-interleaved delivery method that dramatically reduces fluctuations in the delivered transcription factor copy numbers per cell. We screened combinatorial and temporal delivery of a pool of midbrain-specific transcription factors to augment the generation of dopaminergic neurons. We show that the combinatorial delivery of LMX1A, FOXA2 and PITX3 is highly effective in generating dopaminergic neurons from midbrain progenitors. We show that LMX1A significantly increases TH-expression levels when delivered to neural progenitor cells either during proliferation or after induction of neural differentiation, while FOXA2 and PITX3 increase expression only when delivered prior to induction, demonstrating temporal dependence of factor addition." @default.
• W2800140873 created "2018-05-17" @default.
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• W2800140873 date "2018-05-01" @default.
• W2800140873 modified "2023-09-23" @default.
• W2800140873 title "Combinatorial programming of human neuronal progenitors using magnetically-guided stoichiometric mRNA delivery" @default.
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• W2800140873 doi "https://doi.org/10.7554/elife.31922" @default.
• W2800140873 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/5959718" @default.
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