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Defining the diversity of phenotypic respecification using multiple cell lines and reprogramming regimens. | LitMetric

AI Article Synopsis

  • - The study aimed to assess the variability in reprogramming efficiency among similar cell lines by accounting for technical differences and comparing the conversion of these lines to two types of cells: neurons and skeletal muscle.
  • - Results showed that while reprogramming efficiency was consistent within a specific fibroblast line, there were significant differences between different lines, which could explain discrepancies in existing research.
  • - The research indicated that the ability to reprogram cells does not stem from a common subpopulation, as efficiency in converting to one cell type did not predict success in converting to another, suggesting the need for testing multiple cell lines to improve reprogramming outcomes.

Article Abstract

To better understand the basis of variation in cellular reprogramming, we performed experiments with two primary objectives: first, to determine the degree of difference, if any, in reprogramming efficiency among cells lines of a similar type after accounting for technical variables, and second, to compare the efficiency of conversion of multiple similar cell lines to two separate reprogramming regimens-induced neurons and induced skeletal muscle. Using two reprogramming regimens, it could be determined whether converted cells are likely derived from a distinct subpopulation that is generally susceptible to reprogramming or are derived from cells with an independent capacity for respecification to a given phenotype. Our results indicated that when technical components of the reprogramming regimen were accounted for, reprogramming efficiency was reproducible within a given primary fibroblast line but varied dramatically between lines. The disparity in reprogramming efficiency between lines was of sufficient magnitude to account for some discrepancies in published results. We also found that the efficiency of conversion to one phenotype was not predictive of reprogramming to the alternate phenotype, suggesting that the capacity for reprogramming does not arise from a specific subpopulation with a generally "weak grip" on cellular identity. Our findings suggest that parallel testing of multiple cell lines from several sources may be needed to accurately assess the efficiency of direct reprogramming procedures, and that testing a larger number of fibroblast lines--even lines with similar origins--is likely the most direct means of improving reprogramming efficiency.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3780423PMC
http://dx.doi.org/10.1089/scd.2013.0040DOI Listing

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