Matsumoto Y, Ikuta F
Cell Tissue Res. 1985;239(2):271-8. doi: 10.1007/BF00218004.
A study on the localization of fetal and neonatal brain macrophages of mice from embryonic day 10 (E10) to postnatal day 21 (P21) was carried out immunohistochemically using a monoclonal antibody against a macrophage differentiation antigen (Mac-1) and the labeled avidin-biotin technique. In the central nervous system, the macrophages recognized first were mainly located in the choroid plexuses of the fourth and lateral ventricles at E14. Their number increased at E17-P3 and gradually decreased thereafter. In the cerebral parenchyma, a few macrophages appeared at E14 in the matrix cell layer. They were also detected in the migrating zone at E15, E17 and in the cortical plate at E19. Mapping of positive cells at the stage of neuroblast formation (E15, E17, E19) disclosed the precise distribution of cerebral macrophages. The macrophages that appeared first in the choroid plexuses at E15 may be derived from the subarachnoid vessels, which extend into the stroma of the choroid plexuses when the matrix cell layer invaginates into the lateral ventricle to form the choroid plexuses. Almost all of the macrophages recognized in the cerebral parenchyma disappeared at P9 when the cytoarchitecture seemed to be completed. In the cerebellum, which develops later than the cerebrum, macrophages appeared after birth and were located mainly in the internal granular layer. The brain macrophages always appeared in the regions where cell proliferation and brain remodeling are most active at each stage. These findings suggest that fetal and neonatal brain macrophages may play an important role in scavenging degenerated cells and cell debris during histogenesis of the central nervous system.
利用抗巨噬细胞分化抗原(Mac-1)的单克隆抗体和标记抗生物素蛋白-生物素技术,通过免疫组织化学方法对胚胎期第10天(E10)至出生后第21天(P21)的小鼠胎儿和新生儿脑巨噬细胞进行了定位研究。在中枢神经系统中,最早识别出的巨噬细胞主要位于E14时第四脑室和侧脑室的脉络丛。它们的数量在E17 - P3增加,此后逐渐减少。在脑实质中,E14时基质细胞层出现少量巨噬细胞。在E15、E17的迁移区以及E19的皮质板中也检测到了巨噬细胞。在神经母细胞形成阶段(E15、E17、E19)对阳性细胞进行定位,揭示了脑巨噬细胞的精确分布。E15时最早出现在脉络丛中的巨噬细胞可能来源于蛛网膜下血管,当基质细胞层内陷进入侧脑室形成脉络丛时,这些血管延伸至脉络丛的基质。当细胞结构似乎完成时,在P9时脑实质中几乎所有识别出的巨噬细胞都消失了。在比大脑发育晚的小脑中,巨噬细胞在出生后出现,主要位于内颗粒层。脑巨噬细胞总是出现在每个阶段细胞增殖和脑重塑最活跃的区域。这些发现表明,胎儿和新生儿脑巨噬细胞可能在中枢神经系统组织发生过程中清除退化细胞和细胞碎片方面发挥重要作用。