Regenerating CNS myelin: Emerging roles of regulatory T cells and CCN proteins

被引:24
作者
Gallardo, Nira de la Vega [1 ]
Dittmer, Marie [1 ]
Dombrowski, Yvonne [1 ]
Fitzgerald, Denise C. [1 ]
机构
[1] Queens Univ Belfast, Sch Med Dent & Biomed Sci, Wellcome Wolfson Inst Expt Med, Belfast, Antrim, North Ireland
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
Treg; CCN3; Remyelination; Oligodendrocyte; Regeneration; CENTRAL-NERVOUS-SYSTEM; TISSUE GROWTH-FACTOR; MULTIPLE-SCLEROSIS; MOUSE MODEL; OLIGODENDROCYTE DIFFERENTIATION; ADULT CNS; IN-VIVO; REMYELINATION; EXPRESSION; FAMILY;
D O I
10.1016/j.neuint.2018.11.024
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Efficient myelin regeneration in the central nervous system (CNS) requires the migration, proliferation and differentiation of oligodendrocyte progenitor cells (OPC) into myelinating oligodendrocytes. In demyelinating diseases such as multiple sclerosis (MS), this regenerative process can fail, and therapies targeting myelin repair are currently completely lacking in the clinic. The immune system is emerging as a key regenerative player in many tissues, such as muscle and heart. We recently reported that regulatory T cells (Treg) are required for efficient CNS remyelination. Furthermore, Treg secrete CCN3, a matricellular protein from the CCN family, implicated in regeneration of other tissues. Treg-derived CCN3 promoted oligodendrocyte differentiation and myelination. In contrast, previous studies showed that CCN2 inhibited myelination. These studies highlight the need for further scrutiny of the roles that CCN proteins play in myelin development and regeneration. Collectively, these findings open up exciting avenues of research to uncover the regenerative potential of the adaptive immune system.
引用
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页数:10
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