Kakita Akiyoshi, Zerlin Marielba, Takahashi Hitoshi, Goldman James E
Department of Pathology, Center for Neurobiology and Behavior, College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA.
J Comp Neurol. 2003 Apr 14;458(4):381-8. doi: 10.1002/cne.10597.
The great majority of glial cells of the mammalian forebrain are generated in the perinatal period from progenitors in the subventricular zone (SVZ). We investigated the migration of progenitors from the neonatal (postnatal day 0, P0) rat forebrain SVZ by labeling them in vivo with a green fluorescence protein (GFP) retrovirus and monitoring their movements by time-lapse video microscopy in P3 slices. We identified a small number of progenitors that migrated tangentially within the corpus callosum (CC) and crossed the midline. These cells retained a relatively uniform morphology: the leading process was extended toward the contralateral side but showed no process branching or turning away from the migratory direction. Net migration requires the elongation of the leading process and nuclear translocation, and the migrating cells in the CC showed both modes. We confirmed the presence of unmyelinated axon bundles within the P3 CC, but failed to detect any radially directed glial processes (vimentin- or GLAST-immunolabeled fibers) spanning through the CC. Confocal images showed a close proximity between neurofilament-immunolabeled axons and the leading process of the GFP-expressing progenitors in the CC. The destination of the callosal fibers was examined by applying DiI to the right cingulum; the labeled fibers ran throughout the CC and reached the left cingulate and motor areas. The distribution and final fates of the retrovirus-labeled cells were examined in P28 brains. A small proportion of the labeled cells were found in the contralateral hemisphere, where, as oligodendrocytes and astrocytes, they colonized predominantly the cortex and the underlying white matter of the cingulate and secondary motor areas. The distribution pattern appears to coincide well with the projection direction of the callosal fibers. Thus, glial progenitors migrate across the CC, presumably in conjunction with unmyelinated axons, to colonize the contralateral hemisphere.
大多数哺乳动物前脑的神经胶质细胞在围产期由脑室下区(SVZ)的祖细胞产生。我们通过用绿色荧光蛋白(GFP)逆转录病毒在体内标记新生(出生后第0天,P0)大鼠前脑SVZ的祖细胞,并在P3切片中通过延时视频显微镜监测它们的运动,来研究祖细胞的迁移。我们鉴定出少数在前胼胝体(CC)内沿切线方向迁移并穿过中线的祖细胞。这些细胞保持相对一致的形态:前端突起向对侧延伸,但没有突起分支或偏离迁移方向。净迁移需要前端突起的伸长和细胞核转位,CC中的迁移细胞显示出这两种模式。我们证实了P3 CC内存在无髓轴突束,但未能检测到任何穿过CC的径向胶质突起(波形蛋白或GLAST免疫标记纤维)。共聚焦图像显示,CC中神经丝免疫标记的轴突与表达GFP的祖细胞的前端突起紧密相邻。通过将DiI应用于右侧扣带回束来检查胼胝体纤维的目的地;标记的纤维贯穿CC并到达左侧扣带回和运动区。在P28大脑中检查了逆转录病毒标记细胞的分布和最终命运。在对侧半球发现了一小部分标记细胞,它们作为少突胶质细胞和星形胶质细胞,主要定居在扣带回和次级运动区的皮质及下方白质中。这种分布模式似乎与胼胝体纤维的投射方向非常吻合。因此,神经胶质祖细胞可能与无髓轴突一起穿过CC,以定居对侧半球。