Ono Katsuhiko, Yoshii Kengo, Tominaga Hiroyuki, Gotoh Hitoshi, Nomura Tadashi, Takebayashi Hirohide, Ikenaka Kazuhiro
Department of Biology, Kyoto Prefectural University of Medicine, Kyoto, 606-0823, Japan.
Departments of Mathematics, Kyoto Prefectural University of Medicine, Kyoto, Japan.
Brain Struct Funct. 2017 Jul;222(5):2441-2448. doi: 10.1007/s00429-017-1394-2. Epub 2017 Mar 14.
The present study aims to examine the origin of oligodendrocyte progenitor cells (OPCs) in the mouse optic nerve (ON) by labeling OPCs in the fetal forebrain. The labeling of OPCs in the ON was performed by injection of a retrovirus vector carrying the lacZ gene into the lateral ventricle, or by inducible Cre/loxP of Olig2-positive cells. The retrovirus labeling revealed that ventricular zone-derived cells of the fetal forebrain relocated to the ON and differentiated into oligodendrocytes. In addition, lineage tracing of Olig2-positive cells and whole-mount staining of PDGFRα-positive cells demonstrated that OPCs appeared by E12.5 in the preoptic area, and spread caudally to enter the ON. Our results also suggest that OPCs generated during the early stage are depleted from the ON after maturation.
本研究旨在通过标记胎鼠前脑少突胶质前体细胞(OPCs)来研究小鼠视神经(ON)中OPCs的起源。通过将携带lacZ基因的逆转录病毒载体注入侧脑室,或通过诱导性Cre/loxP标记Olig2阳性细胞来标记ON中的OPCs。逆转录病毒标记显示,胎鼠前脑脑室区来源的细胞迁移至ON并分化为少突胶质细胞。此外,对Olig2阳性细胞的谱系追踪和PDGFRα阳性细胞的整体染色表明,OPCs在E12.5时出现在视前区,并向尾侧扩散进入ON。我们的结果还表明,早期产生的OPCs在成熟后会从ON中耗尽。