再髓鞘化
少突胶质细胞
生物
髓鞘
神经科学
祖细胞
人口
祖细胞
脱髓鞘病
转录组
雪旺细胞
细胞生物学
干细胞
中枢神经系统
遗传学
基因表达
基因
人口学
社会学
作者
Minxi Fang,Lixia Chen,Tao Tang,Mengsheng Qiu,Xiaofeng Xu
出处
期刊:Glia
[Wiley]
日期:2023-06-06
卷期号:71 (11): 2499-2510
被引量:24
摘要
Abstract In the central nervous system, oligodendrocytes (OLs) produce myelin sheaths that provide trophic support to neuronal axons and increase the propagation speed of action potential. OLs are constantly generated from OL precursor cells (OPCs) throughout life span. The production of myelinating OLs consists of three canonical stages: OPCs, newly‐formed OLs (NFOs), and mature myelinating OLs. Recently, single‐cell RNA transcriptomic analyses identified a new population of oligodendroglial cells, namely differentiation committed OPCs (COPs). COPs represent a critical intermediate population between OPCs and NFOs, as revealed by specific expression of G‐protein coupled receptor 17 (GPR17). The dysregulation of COPs leads to the remyelination failure in demyelinating diseases and impairs the replacement of lost myelin sheaths due to aging. Hence, understanding the development of COPs and their underlying regulatory network will be helpful in establishing new strategies for promoting myelin repair in demyelinating diseases. This review summarizes the current knowledge on the development and functions of COPs under both physiological and pathological conditions. Overall, COPs function as “checkpoints” to prevent inappropriate precocious OL differentiation and myelination through expressing distinct regulatory factors. Deepening our understanding of COPs may not only advance our knowledge of how OL lineage progresses during development, but also open the door to new treatments for demyelinating diseases.
科研通智能强力驱动
Strongly Powered by AbleSci AI