Kallenbach E
Tissue Cell. 1980;12(1):165-74. doi: 10.1016/0040-8166(80)90059-2.
Adult rats received a single dose of HRP intravenously and were killed from 10 min to 6 hr after injection. Following fixation with glutaraldehyde, the enamel organs were treated with a Graham-Karnovsky-type procedure for peroxidase activity, post-osmicated, and embedded in plastic. Sections were studied with light and electron microscopes. Ten minutes after injection, reaction product was found in all extracellular spaces of the enamel organ, at the enamel-ameloblast interface over smooth-ended and intermediate ameloblasts, and in apical surface invaginations and vesicles of the latter cell types. The enamel-ameloblast interface over the ruffle-ended aemloblasts and the extracellular spaces within the ruffled border were free of reaction product and remained so for up to 6 hr. The apical terminal bars of the ruffle-ended ameloblasts functioned as a barrier to HRP. The basal terminal bars of the smooth-ended ameloblasts likewise seemed to prevent the passage of the HRP. Possibly, HRP flows in a lateral direction from groups of ruffle-ended into groups of smooth-ended ameloblasts. Between 10 min and 6 hr, HRP was cleared more rapidly from the extracellular spaces of the papillary layer than from those of the ameloblast layer, and there was little backflow of tracer from the ameloblast into the papillary layer. Eventually, tracer was cleared also from the extracellular spaces of the ameloblast layer, probably mainly through micropinocytosis by the ameloblasts. A working model is proposed regarding the handling of large molecules by the enamel organ in the maturation zone.
成年大鼠静脉注射单剂量的辣根过氧化物酶(HRP),并在注射后10分钟至6小时处死。用戊二醛固定后,牙釉质器官采用格雷厄姆-卡诺夫斯基(Graham-Karnovsky)型过氧化物酶活性处理方法,进行后固定,然后包埋在塑料中。切片用光学显微镜和电子显微镜进行研究。注射后10分钟,在牙釉质器官的所有细胞外间隙、光滑末端和成釉细胞中间的釉质-成釉细胞界面以及后一种细胞类型的顶端表面内陷和小泡中发现了反应产物。有褶缘成釉细胞上方的釉质-成釉细胞界面以及褶缘内的细胞外间隙没有反应产物,并且在长达6小时内一直如此。有褶缘成釉细胞的顶端终末杆起到了对HRP的屏障作用。光滑末端成釉细胞的基底终末杆同样似乎阻止了HRP的通过。可能,HRP从有褶缘成釉细胞群侧向流入光滑末端成釉细胞群。在10分钟至6小时之间,HRP从乳头层的细胞外间隙清除的速度比从成釉细胞层的细胞外间隙清除的速度更快,并且示踪剂从成釉细胞向乳头层的回流很少。最终,示踪剂也从成釉细胞层的细胞外间隙清除,可能主要是通过成釉细胞的微胞饮作用。提出了一个关于成熟区牙釉质器官对大分子处理的工作模型。