C1q is essential for myelination in the central nervous system (CNS)

被引:4
作者
Yu, Qiang [1 ]
Zhang, Nan [2 ,3 ]
Guan, Teng [1 ]
Guo, Ying [1 ,4 ]
Marzban, Hassan [1 ]
Lindsey, Benjamin [1 ]
Kong, Jiming [1 ]
机构
[1] Univ Manitoba, Dept Human Anat & Cell Sci, Winnipeg, MB, Canada
[2] Hebei Med Univ, Hosp 1, Shijiazhuang, Hebei, Peoples R China
[3] Capital Med Univ, Hebei Hosp, Xuanwu Hosp, Neuromed Technol Innovat Ctr Hebei Prov, Shijiazhuang, Hebei, Peoples R China
[4] Hebei North Univ, Dept Forens Med, Zhangjiakou, Hebei, Peoples R China
基金
中国国家自然科学基金;
关键词
SPINAL-CORD; OLIGODENDROCYTE DEVELOPMENT; IN-VITRO; MICROGLIA; COMPLEMENT; MECHANISMS; NEURONS; HEALTH; ACTIN; FRACTALKINE;
D O I
10.1016/j.isci.2023.108518
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Myelin sheath in the central nervous system (CNS) is essential for efficient action potential conduction. Microglia, the macrophages in the CNS, are suggested to regulate myelin development. However, the specific involvement of microglia in initial myelination is yet to be elucidated. Here, first, by culturing neural stem cells, we demonstrated that myelin sheath formation only occurred in the presence of a microglia-conditioned medium. Furthermore, the absence of C1q, a microglia-derived factor, resulted in myelination failure in the neural stem cell culture. Additionally, adding native human C1q protein was sufficient to induce myelination in vitro. Finally, in the C1q conditional knockout mouse model (C1qa(FL/FL): Cx3cr1(CreER)), C1q deficiency prior to the onset of myelination led to reduced myelin thickness and elevated g-ratio during initial myelination. This study uncovers the pivotal role of microglia-derived C1q in developmental myelination and could potentially pave the way for new therapeutic strategies for treating demyelinating diseases.
引用
收藏
页数:17
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