Department of Molecular Neuroscience, World Premier International Immunology Frontier Research Center, Osaka University, Suita-shi, Osaka, Japan.
Graduate School of Medicine, Osaka University, Suita-shi, Osaka, Japan.
Neuroscientist. 2020 Feb;26(1):74-86. doi: 10.1177/1073858419834221. Epub 2019 Mar 8.
Oligodendrocytes generate myelin sheaths to promote rapid neurotransmission in the central nervous system (CNS). During brain development, oligodendrocyte precursor cells (OPCs) are generated in the medial ganglionic eminence, lateral ganglionic eminence, and dorsal pallium. OPCs proliferate and migrate throughout the CNS at the embryonic stage. After birth, OPCs differentiate into mature oligodendrocytes, which then insulate axons. Oligodendrocyte development is regulated by the extrinsic environment including neurons, astrocytes, and immune cells. During brain development, B lymphocytes are present in the meningeal space, and are involved in oligodendrocyte development by promoting OPC proliferation. T lymphocytes mediate oligodendrocyte development during the remyelination process. Moreover, a subset of microglia contributes to oligodendrocyte development during the neonatal periods. Therefore, the immune system, especially lymphocytes and microglia, contribute to oligodendrocyte development during brain development and remyelination.
少突胶质细胞形成髓鞘以促进中枢神经系统(CNS)中的快速神经传递。在大脑发育过程中,少突胶质前体细胞(OPC)在正中神经隆起、外侧神经隆起和背侧脑区中产生。OPC 在胚胎期增殖并迁移到中枢神经系统的各个部位。出生后,OPC 分化为成熟的少突胶质细胞,然后隔离轴突。少突胶质细胞的发育受包括神经元、星形胶质细胞和免疫细胞在内的外在环境的调节。在大脑发育过程中,B 淋巴细胞存在于脑膜间隙中,通过促进 OPC 增殖来参与少突胶质细胞的发育。T 淋巴细胞在髓鞘再生过程中调节少突胶质细胞的发育。此外,一小部分小胶质细胞在新生儿期有助于少突胶质细胞的发育。因此,免疫系统,特别是淋巴细胞和小胶质细胞,有助于大脑发育和髓鞘再生过程中的少突胶质细胞发育。