Zinc-Finger Protein ZFP488 Regulates the Timing of Oligodendrocyte Myelination and Remyelination

Oligodendrocyte myelination and remyelination after injury are intricately regulated by various intrinsic and extrinsic factors, including transcriptional regulators. Among these, the zinc-finger protein ZFP488 is an oligodendrocyte-enriched transcriptional regulator that promotes oligodendrocyte differentiation in the developing neural tube and in oligodendroglial cell lines. However, the specific in vivo genetic requirements for ZFP488 during oligodendrocyte development and remyelination have not been defined. To address this gap, we generated a lineage-traceable <i>ZFP488</i> knock-out mouse line, wherein an <i>H2b-GFP</i> reporter replaces the <i>ZFP488</i>-coding region. Using these mice of either sex, we examined the dynamics of <i>ZFP488</i> expression from the endogenous promoter in the developing central nervous system (CNS). We observed a unique expression pattern in the oligodendrocyte lineage, with <i>ZFP488</i> expression particularly enriched in differentiated oligodendrocytes. ZFP488 loss resulted in delayed myelination in the developing CNS and impaired remyelination after demyelinating injury in the brain. Integrated transcriptomic and genomic profiling further revealed that ZFP488 loss decreased the expression of myelination-associated genes but not oligodendrocyte progenitor-associated genes, suggesting that ZFP488 serves as a positive regulator of myelination by regulating maturation programs. Thus, our genetic loss-of-function study revealed that ZFP488 regulates a stage-dependent differentiation program that controls the timing of CNS myelination and remyelination.

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Publication Details

Journal
Journal of Neuroscience
Published
2024-08-16
DOI
https://doi.org/10.1523/jneurosci.0141-24.2024
Citations
2
Primary Topic
Neurogenesis and neuroplasticity mechanisms
Type
article
Field-Weighted Citation Impact
0.82

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article

Zinc-Finger Protein ZFP488 Regulates the Timing of Oligodendrocyte Myelination and Remyelination

Yifeng Lin, Chen Dong, Wenhao Zhou, Dazhuan Xin et al.
2 citations
Journal of Neuroscience
Neurogenesis and neuroplasticity mechanisms
0.82
article

Zinc-Finger Protein ZFP488 Regulates the Timing of Oligodendrocyte Myelination and Remyelination

Yifeng Lin, Chen Dong, Wenhao Zhou, Dazhuan Xin, Siying Cui, Fangbing Chen, Xiang Chen, Tong Chen, Qianqian Lü, Huiyao Chen, Xiaowen Zhong
article en
2 citations

Abstract

Oligodendrocyte myelination and remyelination after injury are intricately regulated by various intrinsic and extrinsic factors, including transcriptional regulators. Among these, the zinc-finger protein ZFP488 is an oligodendrocyte-enriched transcriptional regulator that promotes oligodendrocyte differentiation in the developing neural tube and in oligodendroglial cell lines. However, the specific in vivo genetic requirements for ZFP488 during oligodendrocyte development and remyelination have not been defined. To address this gap, we generated a lineage-traceable <i>ZFP488</i> knock-out mouse line, wherein an <i>H2b-GFP</i> reporter replaces the <i>ZFP488</i>-coding region. Using these mice of either sex, we examined the dynamics of <i>ZFP488</i> expression from the endogenous promoter in the developing central nervous system (CNS). We observed a unique expression pattern in the oligodendrocyte lineage, with <i>ZFP488</i> expression particularly enriched in differentiated oligodendrocytes. ZFP488 loss resulted in delayed myelination in the developing CNS and impaired remyelination after demyelinating injury in the brain. Integrated transcriptomic and genomic profiling further revealed that ZFP488 loss decreased the expression of myelination-associated genes but not oligodendrocyte progenitor-associated genes, suggesting that ZFP488 serves as a positive regulator of myelination by regulating maturation programs. Thus, our genetic loss-of-function study revealed that ZFP488 regulates a stage-dependent differentiation program that controls the timing of CNS myelination and remyelination.

Journal of NeuroscienceVol. 44(39)
Cincinnati Children's Hospital Medical Center (US), Children's Hospital of Fudan University (CN)
National Multiple Sclerosis Society, National Natural Science Foundation of China
Openalex Percentile: Top 27%
Neurogenesis and neuroplasticity mechanisms
0.82
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