Microenvironmental Regulation of Central Nervous System Myelination and Remyelination.
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| Title: | Microenvironmental Regulation of Central Nervous System Myelination and Remyelination. |
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| Authors: | Wang, Yuxuan1,2,3, Tan, Lingzhen1,2,3, Lao, Lin1,2,3, Huang, Xiaomeng2, Zhang, Sheng4,5,6 shengzhang@smu.edu.cn, Sun, Haitao1,3,6 2009sht@smu.edu.cn |
| Source: | Journal of Integrative Neuroscience. May2026, Vol. 25 Issue 5, p1-26. 26p. |
| Subjects: | Myelination, Demyelination, Central nervous system, Microglia, Extracellular matrix, Oligodendroglia, Astrocytes |
| Abstract: | Both myelination and remyelination in the central nervous system (CNS) rely on the differentiation of oligodendrocyte precursor cells (OPCs) into mature oligodendrocytes (OLs). However, the microenvironment and underlying mechanisms of these two processes are significantly different. Myelination is driven by intrinsic developmental programs, whereas remyelination is triggered as a response to demyelinating injury. These distinct origins shape unique microenvironmental conditions that critically influence the respective processes. The microenvironment comprises, the extracellular matrix (ECM) and cellular components. Neurons, microglia, and astrocytes play stage-specific roles, ensuring proper myelin turnover under physiological conditions and regeneration after demyelination. Dysregulation of the microenvironment represents a critical driver of aberrant myelination and remyelination failure, as well as a key limitation of current pro-regenerative strategies. In this review, we discuss the cellular and molecular basis of microenvironmental regulation, recent advances in pathological microenvironmental alterations across demyelinating diseases (multiple sclerosis and neuromyelitis optica spectrum disorder) and myelin-associated disorders (Alzheimer's disease and ischemic stroke), and emerging pro-remyelination strategies targeting the microenvironment, such as Bruton's tyrosine kinase (BTK) inhibitors and microglia replacement strategies. We provide a non-cell autonomous perspective to advance the understanding of OLs differentiation and CNS remyelination. [ABSTRACT FROM AUTHOR] |
| Copyright of Journal of Integrative Neuroscience is the property of IMR Press and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
| Database: | Engineering Source |
| FullText | Text: Availability: 0 |
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| Header | DbId: egs DbLabel: Engineering Source An: 194258647 AccessLevel: 6 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Microenvironmental Regulation of Central Nervous System Myelination and Remyelination. – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Wang%2C+Yuxuan%22">Wang, Yuxuan</searchLink><relatesTo>1,2,3</relatesTo><br /><searchLink fieldCode="AR" term="%22Tan%2C+Lingzhen%22">Tan, Lingzhen</searchLink><relatesTo>1,2,3</relatesTo><br /><searchLink fieldCode="AR" term="%22Lao%2C+Lin%22">Lao, Lin</searchLink><relatesTo>1,2,3</relatesTo><br /><searchLink fieldCode="AR" term="%22Huang%2C+Xiaomeng%22">Huang, Xiaomeng</searchLink><relatesTo>2</relatesTo><br /><searchLink fieldCode="AR" term="%22Zhang%2C+Sheng%22">Zhang, Sheng</searchLink><relatesTo>4,5,6</relatesTo><i> shengzhang@smu.edu.cn</i><br /><searchLink fieldCode="AR" term="%22Sun%2C+Haitao%22">Sun, Haitao</searchLink><relatesTo>1,3,6</relatesTo><i> 2009sht@smu.edu.cn</i> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Journal+of+Integrative+Neuroscience%22">Journal of Integrative Neuroscience</searchLink>. May2026, Vol. 25 Issue 5, p1-26. 26p. – Name: Subject Label: Subjects Group: Su Data: <searchLink fieldCode="DE" term="%22Myelination%22">Myelination</searchLink><br /><searchLink fieldCode="DE" term="%22Demyelination%22">Demyelination</searchLink><br /><searchLink fieldCode="DE" term="%22Central+nervous+system%22">Central nervous system</searchLink><br /><searchLink fieldCode="DE" term="%22Microglia%22">Microglia</searchLink><br /><searchLink fieldCode="DE" term="%22Extracellular+matrix%22">Extracellular matrix</searchLink><br /><searchLink fieldCode="DE" term="%22Oligodendroglia%22">Oligodendroglia</searchLink><br /><searchLink fieldCode="DE" term="%22Astrocytes%22">Astrocytes</searchLink> – Name: Abstract Label: Abstract Group: Ab Data: Both myelination and remyelination in the central nervous system (CNS) rely on the differentiation of oligodendrocyte precursor cells (OPCs) into mature oligodendrocytes (OLs). However, the microenvironment and underlying mechanisms of these two processes are significantly different. Myelination is driven by intrinsic developmental programs, whereas remyelination is triggered as a response to demyelinating injury. These distinct origins shape unique microenvironmental conditions that critically influence the respective processes. The microenvironment comprises, the extracellular matrix (ECM) and cellular components. Neurons, microglia, and astrocytes play stage-specific roles, ensuring proper myelin turnover under physiological conditions and regeneration after demyelination. Dysregulation of the microenvironment represents a critical driver of aberrant myelination and remyelination failure, as well as a key limitation of current pro-regenerative strategies. In this review, we discuss the cellular and molecular basis of microenvironmental regulation, recent advances in pathological microenvironmental alterations across demyelinating diseases (multiple sclerosis and neuromyelitis optica spectrum disorder) and myelin-associated disorders (Alzheimer's disease and ischemic stroke), and emerging pro-remyelination strategies targeting the microenvironment, such as Bruton's tyrosine kinase (BTK) inhibitors and microglia replacement strategies. We provide a non-cell autonomous perspective to advance the understanding of OLs differentiation and CNS remyelination. [ABSTRACT FROM AUTHOR] – Name: AbstractSuppliedCopyright Label: Group: Ab Data: <i>Copyright of Journal of Integrative Neuroscience is the property of IMR Press and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.) |
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| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.31083/JIN43257 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 26 StartPage: 1 Subjects: – SubjectFull: Myelination Type: general – SubjectFull: Demyelination Type: general – SubjectFull: Central nervous system Type: general – SubjectFull: Microglia Type: general – SubjectFull: Extracellular matrix Type: general – SubjectFull: Oligodendroglia Type: general – SubjectFull: Astrocytes Type: general Titles: – TitleFull: Microenvironmental Regulation of Central Nervous System Myelination and Remyelination. Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Wang, Yuxuan – PersonEntity: Name: NameFull: Tan, Lingzhen – PersonEntity: Name: NameFull: Lao, Lin – PersonEntity: Name: NameFull: Huang, Xiaomeng – PersonEntity: Name: NameFull: Zhang, Sheng – PersonEntity: Name: NameFull: Sun, Haitao IsPartOfRelationships: – BibEntity: Dates: – D: 01 M: 05 Text: May2026 Type: published Y: 2026 Identifiers: – Type: issn-print Value: 02196352 Numbering: – Type: volume Value: 25 – Type: issue Value: 5 Titles: – TitleFull: Journal of Integrative Neuroscience Type: main |
| ResultId | 1 |