Microglia as therapeutic targets for central nervous system remyelination

被引:13
|
作者
Mahmood, Ayisha [1 ,2 ,3 ]
Miron, Veronique E. [1 ,2 ,3 ]
机构
[1] Univ Edinburgh, United Kingdom Dementia Res Inst, Edinburgh, Midlothian, Scotland
[2] Univ Edinburgh, Ctr Discovery Brain Sci, Chancellors Bldg, Edinburgh, Midlothian, Scotland
[3] Univ Edinburgh, Ctr Reprod Hlth, Queens Med Res Inst, Med Res Council, Edinburgh, Midlothian, Scotland
基金
英国国家替代、减少和改良动物研究中心; 英国医学研究理事会;
关键词
MULTIPLE-SCLEROSIS; MYELIN REPAIR; OLIGODENDROCYTE LINEAGE; MACROPHAGES; MONOCYTES; CELLS; MODEL; DIFFERENTIATION; INFLAMMATION; VARIANTS;
D O I
10.1016/j.coph.2022.102188
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Failed remyelination underpins neurodegeneration and central nervous system (CNS) dysfunction with aging and progression of neurological diseases, such as multiple sclerosis and Alzheimer's disease. Existing therapies have shown limited efficacy in halting disease progression in humans, highlighting the need to identify pro-remyelination treatments. Microglia are CNS-resident macrophages with critical roles in the regulation of remyelination, representing a promising therapeutic target. However, there are currently no therapeutics which specifically target microglia. Recent studies have revealed that microglia are a heterogenous population with distinct transcriptional states in health and disease conditions, including during remyelination, suggesting functional differences between states. Here, we discuss the potential contributions of different microglia states to degenerative and regenerative processes, examine the potential to target microglia in a state-specific manner to promote remyelination and consider the key issues to be addressed before such therapies can be clinically applied.
引用
收藏
页数:8
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