Oligodendrocyte: Development, Plasticity, Biological Functions, Diseases, and Therapeutic Targets

In the past few years, the incidence rate of central nervous system (CNS) diseases is still growing. Meanwhile, the molecular mechanism on the pathogenesis of neurological diseases remains elusive. Oligodendrocyte progenitor cells (OPCs) are distributed in the whole CNS and represent a population of migrating and proliferating adult progenitor oligodendrocytes that can be differentiated into oligodendrocytes (OLs). The main function of OLs is to produce myelin, the membrane wrapping tightly around the axon, which are associated with the myelination and remyelination. During regeneration, the new OLs from OPCs can regenerate lost myelin, which prevents axonal degeneration and restores its plasticity and function. Considering these energy-consuming processes, the high metabolic turnover OLs are susceptible to neurotoxic factors and its excitatory toxicity. Thus, the pathogenesis of OPC and OL are proven in neurological diseases, such as multiple sclerosis, Alzheimer's disease, major psychiatric diseases, and epilepsy. The current study reviewed the development, plasticity as well as application of OPCs and OLs researches on CNS diseases. Additionally, the effective methods and bioengineering technologies as well as biomaterials relevant to regenerative medicine are also discussed, which could provide the novel insight into the therapeutic treatment of those diseases, exploring new pathological clues, identifying the key molecules and targets as well as the potential biomarkers.

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Publication Details

Journal
MedComm
Published
2026-02-01
DOI
https://doi.org/10.1002/mco2.70618
Primary Topic
Neurogenesis and neuroplasticity mechanisms
Type
article
Field-Weighted Citation Impact
0.00

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article

Oligodendrocyte: Development, Plasticity, Biological Functions, Diseases, and Therapeutic Targets

X F Li, Li‐Ni Liu, Jia‐Sheng Tao, Qiong Xiang et al.
MedComm
Neurogenesis and neuroplasticity mechanisms
article

Oligodendrocyte: Development, Plasticity, Biological Functions, Diseases, and Therapeutic Targets

X F Li, Li‐Ni Liu, Jia‐Sheng Tao, Qiong Xiang, Yun Huang, Xianhui Li, Ruo‐Lan Shi
article en

Abstract

In the past few years, the incidence rate of central nervous system (CNS) diseases is still growing. Meanwhile, the molecular mechanism on the pathogenesis of neurological diseases remains elusive. Oligodendrocyte progenitor cells (OPCs) are distributed in the whole CNS and represent a population of migrating and proliferating adult progenitor oligodendrocytes that can be differentiated into oligodendrocytes (OLs). The main function of OLs is to produce myelin, the membrane wrapping tightly around the axon, which are associated with the myelination and remyelination. During regeneration, the new OLs from OPCs can regenerate lost myelin, which prevents axonal degeneration and restores its plasticity and function. Considering these energy-consuming processes, the high metabolic turnover OLs are susceptible to neurotoxic factors and its excitatory toxicity. Thus, the pathogenesis of OPC and OL are proven in neurological diseases, such as multiple sclerosis, Alzheimer's disease, major psychiatric diseases, and epilepsy. The current study reviewed the development, plasticity as well as application of OPCs and OLs researches on CNS diseases. Additionally, the effective methods and bioengineering technologies as well as biomaterials relevant to regenerative medicine are also discussed, which could provide the novel insight into the therapeutic treatment of those diseases, exploring new pathological clues, identifying the key molecules and targets as well as the potential biomarkers.

MedCommVol. 7(2)
Jishou University (CN), Peking University (CN)
Education Department of Hunan Province, China Scholarship Council
Openalex Percentile: Top 69%
Neurogenesis and neuroplasticity mechanisms
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Oligodendrocyte: Development, Plasticity, Biological Functions, Diseases, and Therapeutic Targets — X F Li, Li‐Ni Liu, et al. · MedComm (2026) | TGRS Research Map | TGRS