Josephsen K, Warshawsky H
Am J Anat. 1982 May;164(1):45-56. doi: 10.1002/aja.1001640105.
After injection of labeled precursors such as 3H-proline or 3H-tyrosine into rats, the incisor dentin contains a continuous and stable record of precursor incorporation into labeled proteins. This record was visualized and quantitated with radioautography in order to evaluate the quantitative changes in enamel where newly secreted proteins randomize with older proteins and both are eventually lost. Up to 4 hours after injection, the pulse-dose was incorporated as a highly labeled band of predentin. The band was entirely within calcified dentin at 2 days and was further removed from new predentin by 4 and 8 days. Dentin which formed proximal to the heavily labeled band contained an amount of radioactivity reflecting the level of labeled precursor available at that time. A standardizing factor for experimental error was obtained by quantitating the reaction in the heavily labeled band, and a post-pulse incorporation factor was determined from the amount of radioactivity added per day as weakly labeled dentin. The variation within the heavily labeled band was assumed to reflect experimental error. The number of grains in the bands were averaged from 4 hours to 8 days to give the standardizing factor. This was multiplied by the ratio of enamel to dentin counts in the same section to obtain a corrected enamel count. In this way the coefficient of variation was improved from a high of 17.2% in uncorrected enamel counts to 2.4% in corrected counts. The post-pulse incorporation factor was higher with tyrosine than with proline. With proline it amounted to 5% increase per day from 1 to 4 days and 2.5% per day from 4 to 8 days after injection. In addition, with 3H-proline the incorporation into predentin increased from 30 minutes to 4 hours. With tyrosine, the counts increased from 30 minutes to 1 hour, but decreased by nearly one third from 1 to 4 hours. This was interpreted as a loss of short-lived matrix proteins including procollagen peptides produced during conversion from procollagen to tropocollagen in the predentin.
给大鼠注射如³H - 脯氨酸或³H - 酪氨酸等标记前体后,切牙牙本质包含了前体掺入标记蛋白的连续且稳定的记录。为了评估釉质中的定量变化,利用放射自显影对该记录进行可视化和定量分析,在釉质中,新分泌的蛋白质会与较老的蛋白质随机混合,最终二者都会丢失。注射后长达4小时,脉冲剂量以高度标记的前期牙本质带形式掺入。2天时该带完全位于钙化牙本质内,到4天和8天时则进一步远离新的前期牙本质。在高度标记带近端形成的牙本质所含放射性量反映了当时可用的标记前体水平。通过对高度标记带中的反应进行定量获得实验误差的标准化因子,并根据每天作为弱标记牙本质添加的放射性量确定脉冲后掺入因子。假定高度标记带内的变化反映实验误差。对4小时至8天各带中的颗粒数求平均值以得到标准化因子。将其乘以同一切片中釉质与牙本质计数的比值以获得校正后的釉质计数。通过这种方式,变异系数从未校正的釉质计数中的17.2%的高位改善至校正计数中的2.4%。酪氨酸的脉冲后掺入因子高于脯氨酸。对于脯氨酸,注射后1至4天每天增加5%,4至8天每天增加2.5%。此外,用³H - 脯氨酸时,前期牙本质中的掺入从30分钟到4小时增加。对于酪氨酸,计数从30分钟到1小时增加,但从1到4小时减少了近三分之一。这被解释为前期牙本质中从原胶原转化为原纤维胶原过程中产生的包括原胶原肽在内的短寿命基质蛋白的丢失。