ArticleJournal of cellular and molecular medicine2012
Cellular diversity within embryonic stem cells: pluripotent clonal sublines show distinct differentiation potential.
Article in Journal of cellular and molecular medicine, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
9 citing papers in PubMed.
- Robotic High-Throughput Biomanufacturing and Functional Differentiation of Human Pluripotent Stem Cells.bioRxiv : the preprint server for biology · 2020Article
- Mitochondria structural reorganization during mouse embryonic stem cell derivation.Protoplasma · 2018Article
- Comparison ofFrontiers in molecular neuroscience · 2018Article
- Article
- Glucocorticoid receptor represses brain-derived neurotrophic factor expression in neuron-like cells.Molecular brain · 2017Article
- Generation of mouse induced pluripotent stem cells by protein transduction.Tissue engineering. Part C, Methods · 2014Article
- Generation of neuronal progenitor cells and neurons from mouse sleeping beauty transposon-generated induced pluripotent stem cells.Cellular reprogramming · 2012Article
- Review
- Generation and applications of human pluripotent stem cells induced into neural lineages and neural tissues.Frontiers in physiology · 2012Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Embryonic stem cells (ESC), derived from the early inner cell mass (ICM), are constituted of theoretically homogeneous pluripotent cells. Our study was designed to test this concept using experimental approaches that allowed characterization of progenies derived from single parental mouse ESC. Flow cytometry analysis showed that a fraction of ESC submitted to neural differentiation generates progenies that escape the desired phenotype. Live imaging of individual cells demonstrated significant variations in the capacity of parental ESC to generate neurons, raising the possibility of clonal diversity among ESC. To further substantiate this hypothesis, clonal sublines from ESC were generated by limit dilution. Transcriptome analysis of undifferentiated sublines showed marked differences in gene expression despite the fact that all clones expressed pluripotency markers. Sublines showed distinct differentiation potential, both in phenotypic differentiation assays and with respect to gene expression in embryoid bodies. Clones generated from another ESC line also showed individualities in their differentiation potential, demonstrating the wider applicability of these findings. Taken together, our observations demonstrate that pluripotent ESC consist of individual cell types with distinct differentiation potentials. These findings identify novel elements for the biological understanding of ESC and provide new tools with a major potential for their future in vitro and in vivo use.
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Registered trials
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