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MicroRNA-23a promotes myelination in the central nervous system
Open accessAbstract
Demyelinating disorders including leukodystrophies are devastating conditions that are still in need of better understanding, and both oligodendrocyte differentiation and myelin synthesis pathways are potential avenues for developing treatment. Overexpression of lamin B1 leads to leukodystrophy characterized by demyelination of the central nervous system, and microRNA-23 (miR-23) was found to suppress lamin B1 and enhance oligodendrocyte differentiation in vitro. Here, we demonstrated that miR-23a-overexpressing mice have increased myelin thickness, providing in vivo evidence that miR-23a enhances both oligodendrocyte differentiation and myelin synthesis. Using this mouse model, we explored possible miR-23a targets and revealed that the phosphatase and tensin homologue/phosphatidylinositol trisphosphate kinase/Akt/mammalian target of rapamycin pathway is modulated by miR-23a. Additionally, a long noncoding RNA, 2700046G09Rik, was identified as a miR-23a target and modulates phosphatase and tensin homologue itself in a miR-23a-dependent manner. The data presented here imply a unique role for miR-23a in the coordination of proteins and noncoding RNAs in generating and maintaining healthy myelin.
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“it can inhibit the expression of lamin B1 to protect against leukodystrophy characterized by demyelination of the central nervous system.”
From Recent advances of miR-23 in human diseases and growth development (2025) · cites this paper as [134]
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“Experimental loss of miR-23a reduces myelin gene expression and increases OL susceptibility to stress (Lin et al., 2013).”
From Cell-specific MicroRNA networks orchestrate the pathogenesis of Alzheimer’s disease (2026) · cites this paper as Lin et al., 2013
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“While direct AD-specific data for miR-23a/b remain limited, converging transcriptomic studies consistently report dysregulation of myelin-regulatory pathways in AD white matter, suggesting indirect relevance within OL-mediated degeneration (Nasrabady et al., 2018; Lin et al., 2013; Zhou et al., 2022).”
From Cell-specific MicroRNA networks orchestrate the pathogenesis of Alzheimer’s disease (2026) · cites this paper as Lin et al., 2013
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“LncRNA 2700046G09Rik was targeted by miR-23a to modulate phosphatase and tensin homolog and maintain normal myelin function [133,134].”
From Recent advances of miR-23 in human diseases and growth development (2025) · cites this paper as [134]
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“overexpressing miR-23a in mice was observed as the thickness of myelin increases”
From Recent advances of miR-23 in human diseases and growth development (2025) · cites this paper as [134]
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“The hsa-miR-221/222 family, involved in neuroinflammation [49][50][51] , was enriched both in neurons and microglia (Supplementary Figure 2e).”
From Human brain microRNAs exhibit cell-type specificity and age dependence (2026) · cites this paper as [49]
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“Furthermore, miR-23a/b is required for maintaining OPC and OL survival and nuclear integrity.”
From Cell-specific MicroRNA networks orchestrate the pathogenesis of Alzheimer’s disease (2026) · cites this paper as Lin et al., 2013
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Metadata
- Authors
- Lin, S.-T., Huang, Y., Zhang, L., Heng, M. Y., Ptáček, L. J., & Fu, Y.-H.
- Affiliations
- Department of Neurology and
- Howard Hughes Medical Institute (US)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2013-10-07
- Volume
- 110
- Issue
- 43
- Pages
- 17468-17473
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC3808585
- OpenAlex
- W2071512787
- Cited by
- 117
- References
- 39
- Citations by year
- 2026: 8 · 2025: 3 · 2024: 10 · 2023: 9 · 2022: 7 · 2021: 9 · 2020: 13 · 2019: 20 · 2018: 3 · 2017: 9 · 2016: 9 · 2015: 9 · 2014: 8
- FWCI
- 3.22
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- eScholarship (California Digital Library) (submittedVersion)
- Funders
- Howard Hughes Medical Institute
- National Institutes of Health
- National Institute of Diabetes and Digestive and Kidney Diseases (P30DK063720)
- National Institute of Neurological Disorders and Stroke (NS062733, R01NS062733)
- Topics
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › MicroRNA in disease regulation
- Health Sciences › Medicine › Clinical Neurology › Multiple Sclerosis Research Studies
- Keywords
- microRNA-23a, myelination, oligodendrocyte differentiation, lamin B1, leukodystrophy, demyelination, myelin synthesis, microRNA target regulation, central nervous system
- MeSH terms
- Animals, Cell Differentiation, Cells, Cultured, Central Nervous System, Humans, Mice, Inbred C57BL, Mice, Transgenic, Microscopy, Electron, Myelin Sheath, Oligodendroglia, Blotting, Western, Signal Transduction, Reverse Transcriptase Polymerase Chain Reaction, MicroRNAs, Proto-Oncogene Proteins c-akt, PTEN Phosphohydrolase, Mice, HEK293 Cells, TOR Serine-Threonine Kinases, Transcriptome, RNA, Long Noncoding
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