Warshawsky H
J Biol Buccale. 1979 Mar;7(1):105-26.
Radioautography has been used to visualize various aspects of morphogenesis and differentiation in the continuously erupting rat incisor. Formation of the entire incisor involves continuous production of "tooth segments" at the growing end of the tooth, each of which undergoes a similar history of development as it is carried by eruption towards the oral cavity. The sequence of differentiation which characterizes the life cycle of the ameloblasts was timed using 3H-thymidine, a precursor of DNA. The cells pass through presecretory, secretory and maturative stages whose collective activity results in the layer of mature enamel. 3H-Amino acids, as precursors of proteins were used to evaluate the protein synthetic activity of ameloblasts, before, during and after they produced the layer of enamel. Quantitative analysis (grain counts) of the differential utilization of 3H-proline and 3H-tyrosine by the various types of ameloblasts suggests that the cells produce structural proteins throughout their life cycle, but they produce enamel proteins only in the zone of secretion. The data further suggest that near the end of the presecretory zone structural proteins are used in the formation of Tomes' processes and that during secretion structural proteins contribute to the persistent growth of those processes as the rods are lengthening. Sugars such as 3H-N-acetylmannosamine and 3H-fucose were used to examine glycoprotein formation by ameloblasts. In the secretion zone labeled glycoproteins were not present in the enamel layer, but were confined to the cell bodies and Tomes' processes of ameloblasts at time intervals up to 4 hours after injection. This was contrary to the behaviour of extracellular proteins labeled with 3H-amino acids which left the cell and were present in the enamel at similar time intervals. The distribution of labeled sugars was indicative of turnover of membrane-associated glycoprotein possibly related to growth. This was interpreted as further support for the concept of a lengthening Tomes' process which remains embedded in the enamel until it is obliterated by the forming rod. Preliminary attempts were made to define the role of hormones in tooth development. Specific receptor sites for 125I-insulin were localized to the endothelial lining of capillaries in the papillary layer during maturation. Although the significance is unclear, the potential of this tool in studying dental morphogenesis is considerable.
放射自显影术已被用于观察持续萌出的大鼠切牙形态发生和分化的各个方面。整个切牙的形成涉及在牙的生长端持续产生“牙段”,每个牙段在向口腔萌出的过程中经历相似的发育历程。利用DNA前体3H-胸腺嘧啶核苷对成釉细胞生命周期中特征性的分化序列进行了计时。细胞经历前分泌、分泌和成熟阶段,这些阶段的共同活动产生成熟釉质层。3H-氨基酸作为蛋白质的前体,用于评估成釉细胞在产生釉质层之前、期间和之后的蛋白质合成活性。对不同类型成釉细胞对3H-脯氨酸和3H-酪氨酸的差异利用进行定量分析(颗粒计数)表明,细胞在其整个生命周期中都产生结构蛋白,但仅在分泌区产生釉质蛋白。数据还表明,在前分泌区末端附近,结构蛋白用于形成托姆斯突,并且在分泌过程中,随着釉柱延长,结构蛋白有助于这些突起的持续生长。诸如3H-N-乙酰甘露糖胺和3H-岩藻糖等糖类被用于检测成釉细胞的糖蛋白形成。在分泌区,注射后长达4小时的时间间隔内,标记的糖蛋白不存在于釉质层中,而是局限于成釉细胞的细胞体和托姆斯突。这与用3H-氨基酸标记的细胞外蛋白的行为相反,后者在相似的时间间隔离开细胞并存在于釉质中。标记糖的分布表明膜相关糖蛋白可能与生长相关的周转。这被解释为对托姆斯突延长概念的进一步支持,托姆斯突在被形成的釉柱消除之前一直嵌入釉质中。已初步尝试确定激素在牙齿发育中的作用。在成熟过程中,125I-胰岛素的特异性受体位点定位于乳头层毛细血管的内皮衬里。尽管其意义尚不清楚,但该工具在研究牙齿形态发生方面的潜力相当大。