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  Expression of Lineage Transcription Factors Identifies Differences in Transition States of Induced Human Oligodendrocyte Differentiation

Raabe, F. J., Stephan, M., Waldeck, J. B., Huber, V., Demetriou, D., Kannaiyan, N., et al. (2022). Expression of Lineage Transcription Factors Identifies Differences in Transition States of Induced Human Oligodendrocyte Differentiation. CELLS, 11(2): 241. doi:10.3390/cells11020241.

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 Creators:
Raabe, Florian J.1, Author           
Stephan, Marius1, Author           
Waldeck, Jan Benedikt, Author
Huber, Verena, Author
Demetriou, Damianos, Author
Kannaiyan, Nirmal, Author
Galinski, Sabrina, Author
Glaser, Laura V., Author
Wehr, Michael C., Author
Ziller, Michael J.2, Author           
Schmitt, Andrea, Author
Falkai, Peter, Author
Rossner, Moritz J., Author
Affiliations:
1IMPRS Translational Psychiatry, Max Planck Institute of Psychiatry, Max Planck Society, ou_3318616              
2RG Genomics of Complex Diseases, Max Planck Institute of Psychiatry, Max Planck Society, ou_3008285              

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 Abstract: Oligodendrocytes (OLs) are critical for myelination and are implicated in several brain disorders. Directed differentiation of human-induced OLs (iOLs) from pluripotent stem cells can be achieved by forced expression of different combinations of the transcription factors SOX10 (S), OLIG2 (O), and NKX6.2 (N). Here, we applied quantitative image analysis and single-cell transcriptomics to compare different transcription factor (TF) combinations for their efficacy towards robust OL lineage conversion. Compared with S alone, the combination of SON increases the number of iOLs and generates iOLs with a more complex morphology and higher expression levels of myelin-marker genes. RNA velocity analysis of individual cells reveals that S generates a population of oligodendrocyte-precursor cells (OPCs) that appear to be more immature than those generated by SON and to display distinct molecular properties. Our work highlights that TFs for generating iOPCs or iOLs should be chosen depending on the intended application or research question, and that SON might be beneficial to study more mature iOLs while S might be better suited to investigate iOPC biology.

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 Dates: 2022-01
 Publication Status: Published online
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 Identifiers: ISI: 000757660600001
DOI: 10.3390/cells11020241
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Title: CELLS
Source Genre: Journal
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Pages: - Volume / Issue: 11 (2) Sequence Number: 241 Start / End Page: - Identifier: -