Karim A, Warshawsky H
Am J Anat. 1984 Mar;169(3):327-35. doi: 10.1002/aja.1001690308.
This study was designed to study the time course of the incorporation of 55Fe into the ameloblasts of maturation in rat incisors. Male Sherman rats (100 +/- 5 gm) were injected intravenously with 0.9 mCi of 55Fe and sacrificed in pairs by perfusion at various time intervals from 5 min to 7 days after injection. The incisors were demineralized in 4.13% disodium EDTA, postfixed in 1% osmium tetroxide in veronal acetate buffer, and embedded in Epon. Incisors from control rats injected with only physiological saline were treated in the same way. Sections from blocks of tissue in the zone of maturation were prepared for light microscope radioautographic observations. The greatest incorporation of iron occurred at 9 mm within the zone; at this site the ameloblasts contained few pigment granules. About 5 mm deeper into the zone the activity fell off to zero, as observed at 2.5 hr after injection of 55Fe. Between 1 day and 7 days after injection the 55Fe labeling was found over the cells containing many pigment granules, while the initial labeling over the cells within 9 mm of the zone had diminished. These data have shown that at any given time, from 30 min to 4 hr, the iron enters the maturation ameloblasts over a wide extent of the zone, reaching a maximum at about 9 mm from the onset of maturation. However, at longer times (1 day to 7 days) the labeling curve shifts and shows the greatest activity beyond 9 mm within the zone.
本研究旨在探讨55Fe掺入大鼠切牙成熟成釉细胞的时间进程。雄性谢尔曼大鼠(体重100±5克)静脉注射0.9毫居里的55Fe,并在注射后5分钟至7天的不同时间间隔成对处死,通过灌注法取材。切牙在4.13%的乙二胺四乙酸二钠中脱矿,然后在醋酸巴比妥缓冲液中用1%的四氧化锇后固定,再包埋于环氧树脂中。仅注射生理盐水的对照大鼠的切牙也按同样方法处理。制备成熟区组织块的切片,用于光学显微镜放射自显影观察。铁的掺入量在该区域内9毫米处最高;在此部位,成釉细胞含有的色素颗粒很少。注射55Fe后2.5小时观察到,在该区域再深入约5毫米处,活性降至零。注射后1天至7天,在含有许多色素颗粒的细胞上发现有55Fe标记,而该区域内9毫米范围内细胞上的初始标记减少。这些数据表明,在任何给定时间,从30分钟到4小时,铁在该区域的很大范围内进入成熟的成釉细胞,在距成熟开始约9毫米处达到最大值。然而,在更长时间(1天至7天),标记曲线发生移动,显示该区域内9毫米以外的活性最高。