Profiling miRNAs involved in Human Oligodendrocyte Precursor Cell Differentiation and Maturation

MicroRNAs (miRNAs) are evolutionarily conserved post-transcriptional regulators that play critical roles in cellular development and differentiation across species. Although the importance of miRNAs in oligodendrocyte lineage cell (OLLC) differentiation has been extensively studied in rodent models, their roles in human OL development remain less understood. To address this gap, we used a human embryonic stem cell (hESC) reporter system designed to study human OLs and OL progenitor cells (OPCs). Using an optimized differentiation protocol, we used the reporter hESCs to generate and isolate well-characterized OLLCs at specific developmental stages and performed next-generation sequencing-based miRNA profiling to identify stage-specific miRNAs enriched during OL lineage specification and maturation. In addition to canonical miRNAs known to be enriched at various stages of OL development, our study identified several lesser-known miRNAs with distinct stage-specific enrichment patterns that may serve as useful molecular markers for classifying human CNS cell types in future studies. Target analysis of OPC- and OL-enriched miRNAs revealed key genes, including transcription factors ZNF488 and DLX1, cytoskeletal regulator CSNK2B, and potassium channel gene KCNJ1, along with key signaling pathways such as AKT, SMAD2/3, estrogen receptor, and insulin signaling, which regulate OPC and OL lineage function. These findings advance our understanding of the OLLC-specific miRNAs, and miRNA-mediated regulatory networks governing human OL differentiation and maturation and provide promising therapeutic targets for future studies aimed at restoring myelin integrity and improving outcomes in demyelinating diseases.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2025-12-26
DOI
https://doi.org/10.64898/2025.12.25.696416
Primary Topic
Neurogenesis and neuroplasticity mechanisms
Type
article
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article

Profiling miRNAs involved in Human Oligodendrocyte Precursor Cell Differentiation and Maturation

Samarjit Das, Xitiz Chamling, Donald J. Zack, Asmita Dhukhwa et al.
bioRxiv (Cold Spring Harbor Laboratory)
Neurogenesis and neuroplasticity mechanisms
article

Profiling miRNAs involved in Human Oligodendrocyte Precursor Cell Differentiation and Maturation

Samarjit Das, Xitiz Chamling, Donald J. Zack, Asmita Dhukhwa, Arun H. Patil, Fernanda Carrizo Velásquez, Mansoureh Barzegar, Vaidehi Nilesh Patel, Marc K Halushka
article en

Abstract

MicroRNAs (miRNAs) are evolutionarily conserved post-transcriptional regulators that play critical roles in cellular development and differentiation across species. Although the importance of miRNAs in oligodendrocyte lineage cell (OLLC) differentiation has been extensively studied in rodent models, their roles in human OL development remain less understood. To address this gap, we used a human embryonic stem cell (hESC) reporter system designed to study human OLs and OL progenitor cells (OPCs). Using an optimized differentiation protocol, we used the reporter hESCs to generate and isolate well-characterized OLLCs at specific developmental stages and performed next-generation sequencing-based miRNA profiling to identify stage-specific miRNAs enriched during OL lineage specification and maturation. In addition to canonical miRNAs known to be enriched at various stages of OL development, our study identified several lesser-known miRNAs with distinct stage-specific enrichment patterns that may serve as useful molecular markers for classifying human CNS cell types in future studies. Target analysis of OPC- and OL-enriched miRNAs revealed key genes, including transcription factors ZNF488 and DLX1, cytoskeletal regulator CSNK2B, and potassium channel gene KCNJ1, along with key signaling pathways such as AKT, SMAD2/3, estrogen receptor, and insulin signaling, which regulate OPC and OL lineage function. These findings advance our understanding of the OLLC-specific miRNAs, and miRNA-mediated regulatory networks governing human OL differentiation and maturation and provide promising therapeutic targets for future studies aimed at restoring myelin integrity and improving outcomes in demyelinating diseases.

bioRxiv (Cold Spring Harbor Laboratory)
Cleveland Clinic (US), Johns Hopkins University (US), Johns Hopkins Medicine (US), Johns Hopkins University Applied Physics Laboratory (US), Lieber Institute for Brain Development (US)
Openalex Percentile: Top 29%
Neurogenesis and neuroplasticity mechanisms
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