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SOX10 Overexpression Enhances the Oligodendrocyte Lineage Commitment of iOPCs In Vitro by Reshaping Their Chromatin Binding Landscape.

Overview

Authors: Fan Zhang1,2, Zhaoyan Wang1, Dou Ye1,2, Jialan Liang1,2, Hui Yang1, Suqing Qu1, Qian Wang1, Zuo Luan1,2
ORCID iDs: Fan Zhang
  1. Department of Pediatrics, The Sixth Medical Center of PLA General Hospital, Beijing 100048, China
  2. Medical School of Chinese PLA, Beijing 100853, China
Institutions: Chinese PLA General Hospital (China)
Journal: Bioengineering (Basel, Switzerland), volume 13, issue 5, article 500
Dates: received 16 March 2026; accepted 21 April 2026; published online 25 April 2026
Type: Research article · Language: English
License: CC BY
Identifiers: DOI 10.3390/bioengineering13050500 · PMID 42194257 · PMCID PMC13203712 · OpenAlex W7159783383
Open access: gold, a free copy (OpenAlex)
Status: data only
Categories: genetics / omics (modality), cellular / molecular (subfield)
Methods: Statistics
Keywords: OPC, oligodendrocyte, differentiation, transcription factor, SOX10
Topic: Neurogenesis and neuroplasticity mechanisms (Developmental Neuroscience, Neuroscience), according to OpenAlex
Funding: National Key Research and Development Program (2018YFA0108601)
Citations: not cited yet (Europe PMC); 48 references in the paper

Abstract

Although transplantation of induced oligodendrocyte progenitor cells (iOPCs) is a promising strategy for white matter injury, the therapeutic efficacy of in vitro-generated iOPCs remains limited due to insufficient differentiation potential. Here, we aimed to identify key transcription factors and small-molecule drugs to optimize iOPC quality. Through transcriptome sequencing and bioinformatics analysis, we identified the transcription factor SOX10, which is differentially expressed between endogenous fetal OPCs and exogenous iOPCs. We established lentivirus-mediated SOX10 overexpression in neural stem cells (NSCs) before iOPC induction and performed cellular assays and multi-omics analysis. Early SOX10 overexpression reduced cell migration but promoted maturation into oligodendrocytes and suppressed astrocyte differentiation. Multi-omics analyses revealed that SOX10 overexpression is associated with the extensive redistribution of SOX10 chromatin binding and enrichment of regulatory programs linked to oligodendroglial differentiation, including the activation of the key signaling downstream transcription factors JUN/FOS. Moreover, TSA, Dabrafenib, and Fedratinib effectively upregulated SOX10 and improved iOPC differentiation. This study identifies SOX10 as a core upstream regulator governing the fate of iOPCs, providing a potential strategy for optimizing iOPC induction for future investigation of white matter injury therapy.

Reproduced under the paper's license (CC BY), from the paper cited above.

Code

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Data

Datasets cited

Data Availability Statement

The raw ATAC-seq, ChIP-seq, and RNA-seq data generated in this study have been deposited in the GSA-human database under accession number HRA017540 and will be made available upon reasonable request.

Reproduced under the paper's license (CC BY), from the paper cited above.

Versions

The history of this record: each version stored by the harvester or made by a correction of its authors or of the maintainers of its code, and what changed in its facts. The texts of the paper (its abstract, its availability statements) are not part of it; versions that changed only those are not listed.

Version 1, 30 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 8 authors, 5 keywords, 1 funder, 47 references.

Cite

This paper

Zhang, F., Wang, Z., Ye, D., Liang, J., Yang, H., Qu, S., Wang, Q., & Luan, Z. (2026). SOX10 Overexpression Enhances the Oligodendrocyte Lineage Commitment of iOPCs In Vitro by Reshaping Their Chromatin Binding Landscape. Bioengineering (Basel, Switzerland), 13(5), 500. https://doi.org/10.3390/bioengineering13050500

BibTeX

@article{zhang2026sox10,
author = {Zhang, Fan and Wang, Zhaoyan and Ye, Dou and Liang, Jialan and Yang, Hui and Qu, Suqing and Wang, Qian and Luan, Zuo},
title = {{SOX10 Overexpression Enhances the Oligodendrocyte Lineage Commitment of iOPCs In Vitro by Reshaping Their Chromatin Binding Landscape}},
journal = {Bioengineering (Basel, Switzerland)},
year = {2026},
month = apr,
volume = {13},
number = {5},
pages = {500},
publisher = {Multidisciplinary Digital Publishing Institute (MDPI)},
issn = {2306-5354},
doi = {10.3390/bioengineering13050500},
url = {https://doi.org/10.3390/bioengineering13050500},
pmid = {42194257},
pmcid = {PMC13203712}
}

RIS

TY - JOUR
AU - Zhang, Fan
AU - Wang, Zhaoyan
AU - Ye, Dou
AU - Liang, Jialan
AU - Yang, Hui
AU - Qu, Suqing
AU - Wang, Qian
AU - Luan, Zuo
TI - SOX10 Overexpression Enhances the Oligodendrocyte Lineage Commitment of iOPCs In Vitro by Reshaping Their Chromatin Binding Landscape
T2 - Bioengineering (Basel, Switzerland)
J2 - Bioengineering (Basel)
PY - 2026
DA - 2026/04/25
VL - 13
IS - 5
SP - 500
SN - 2306-5354
PB - Multidisciplinary Digital Publishing Institute (MDPI)
DO - 10.3390/bioengineering13050500
UR - https://doi.org/10.3390/bioengineering13050500
LA - en
ER -

CSL-JSON

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"container-title": "Bioengineering (Basel, Switzerland)",
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"ISSN": "2306-5354",
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"language": "en",
"issued": {
"date-parts": [
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