Epigenetic and transcriptional shifts in human neural stem cells after reprogramming into induced pluripotent stem cells and subsequent redifferentiation
Induced pluripotent stem cells (iPSCs) and their derivatives have been described to display epigenetic memory of their founder cells, as well as de novo reprogramming-associated alterations. In order to selectively explore changes due to the reprogramming process and not to heterologous somatic memo...
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| Main Authors: | , , , , , , |
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| Format: | Article (Journal) |
| Language: | English |
| Published: |
12 March 2024
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| In: |
International journal of molecular sciences
Year: 2024, Volume: 25, Issue: 6, Pages: 1-15 |
| ISSN: | 1422-0067 |
| DOI: | 10.3390/ijms25063214 |
| Online Access: | Verlag, kostenfrei, Volltext: https://doi.org/10.3390/ijms25063214 Verlag, kostenfrei, Volltext: https://www.mdpi.com/1422-0067/25/6/3214 
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| Author Notes: | Carolin Haubenreich, Michael Lenz, Andreas Schuppert, Michael Peitz, Philipp Koch, Martin Zenke and Oliver Brüstle |
| Summary: | Induced pluripotent stem cells (iPSCs) and their derivatives have been described to display epigenetic memory of their founder cells, as well as de novo reprogramming-associated alterations. In order to selectively explore changes due to the reprogramming process and not to heterologous somatic memory, we devised a circular reprogramming approach where somatic stem cells are used to generate iPSCs, which are subsequently re-differentiated into their original fate. As somatic founder cells, we employed human embryonic stem cell-derived neural stem cells (NSCs) and compared them to iPSC-derived NSCs derived thereof. Global transcription profiling of this isogenic circular system revealed remarkably similar transcriptomes of both NSC populations, with the exception of 36 transcripts. Amongst these we detected a disproportionately large fraction of X chromosomal genes, all of which were upregulated in iPSC-NSCs. Concurrently, we detected differential methylation of X chromosomal sites spatially coinciding with regions harboring differentially expressed genes. While our data point to a pronounced overall reinstallation of autosomal transcriptomic and methylation signatures when a defined somatic lineage is propagated through pluripotency, they also indicate that X chromosomal genes may partially escape this reinstallation process. Considering the broad application of iPSCs in disease modeling and regenerative approaches, such reprogramming-associated alterations in X chromosomal gene expression and DNA methylation deserve particular attention. |
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| Item Description: | Gesehen am 21.08.2024 |
| Physical Description: | Online Resource |
| ISSN: | 1422-0067 |
| DOI: | 10.3390/ijms25063214 |