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(35S)硫酸盐双重掺入大鼠磨牙中作为矿化促进剂的牙本质蛋白聚糖和前期牙本质蛋白聚糖中。

Dual incorporation of (35S)sulfate into dentin proteoglycans acting as mineralization promotors in rat molars and predentin proteoglycans.

作者信息

Lormée P, Septier D, Lécolle S, Baudoin C, Goldberg M

机构信息

Facult-e de Chirurgie Dentaire, Universit-e Ren-e Descartes-Paris V 1 rue Maurice Arnoux 92120 Maurice Arnoux 92120 Montrouge, France.

出版信息

Calcif Tissue Int. 1996 May;58(5):368-75. doi: 10.1007/BF02509387.

Abstract

Autoradiographic investigations were carried out 0.5, 1, 2, 4, 24, 48, 72, and 120 hours after the injection of a single dose of [35S]-sulfate on undemineralized molars of 7-15-day-old rats. In predentin, labeling was detected at 0.5 hours. Silver grain density reached a plateau value between 1 and 24 hours, then decreased and disappeared 120 hours after injection. In dentin, the mineralization front started to be labeled as early as 0.5 hours after injection. Labeling increased at the dentin edge between 1 and 2 hours, reached a maxima at 4 hours, then started to decrease, the labeled band seen 24 hours after injection being further incorporated into dentin. This band stood at constant distance from the dentin-enamel junction with stable grain density, even at 120 hours. This investigation proves the existence of two distinct groups of [35S]-labeled proteoglycans, one exclusively related to predentin and disappearing with time, and the second one located in dentin behaves as a stable component. The fact that an early labeling appeared at the mineralization front which was further incorporated into dentin, confirms that dentin proteoglycans constitute an individual group of molecules that are not derived from predentin proteoglycans, and act as mineralization promotors.

摘要

在给7至15日龄大鼠的未脱矿磨牙注射单剂量的[35S]-硫酸盐后0.5、1、2、4、24、48、72和120小时进行了放射自显影研究。在前期牙本质中,0.5小时时检测到标记。银颗粒密度在1至24小时之间达到平台值,然后下降并在注射后120小时消失。在牙本质中,矿化前沿在注射后0.5小时就开始被标记。标记在1至2小时之间在牙本质边缘增加,在4小时达到最大值,然后开始下降,注射后24小时看到的标记带进一步并入牙本质。即使在120小时时,这条带与牙本质-釉质界保持恒定距离,颗粒密度稳定。这项研究证明存在两组不同的[35S]标记的蛋白聚糖,一组仅与前期牙本质相关并随时间消失,另一组位于牙本质中,表现为稳定成分。矿化前沿早期出现标记并进一步并入牙本质这一事实,证实牙本质蛋白聚糖构成了一组独立的分子,它们并非源自前期牙本质蛋白聚糖,并作为矿化促进剂发挥作用。

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