秋水仙碱对鼠兔成牙细胞超微结构的影响。

K Prostak, P Seifert, Z Skobe
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引用次数: 10

摘要

研究了秋水仙碱诱导的成牙细胞在牙釉质基质形成过程中的超微结构变化。经处理的牙内上皮(IDE)细胞在任何剂量水平或时间间隔内均未表现出颗粒内质网(GER)池的扩张,也未积累高尔基相关的分泌颗粒。这种反应明显不同于硬骨鱼IDE细胞合成釉质胶原基质时所观察到的反应。与对照组相比,处理过的滑冰IDE细胞确实显示出含糖原囊泡和与无定形物质相关的细胞间糖原的积累增加。此外,大量细胞内糖原池和无定形物质的异常出现表明碳水化合物加工是skate IDE细胞的主要功能。与类釉质基质形成相关的治疗成牙细胞有时显示GER池扩张,但未观察到前胶原分泌颗粒。相反,电子致密物质存在于高尔基池、管状颗粒和大颗粒中。在处理过的成牙细胞中,一些电子致密物质似乎通过多泡体分流到吸收途径。管状颗粒与类搪瓷基质的连续性表明它们含有类搪瓷基质的前体,可能是周期性的,17.5 nm的横纹“巨型”纤维。与牙本质前胶原基质沉积相关的经处理成牙本质细胞显示GER池扩张和前胶原分泌颗粒积聚,这与活性胶原合成和分泌功能一致。结果表明:(1)在硬骨鱼牙齿发育过程中,skate IDE细胞不能合成釉质样胶原;(2) skate IDE细胞确实加工糖原分泌到类釉质基质中;(3)胶原蛋白虽然存在,但并不是滑冰釉样基质的主要成分;(4)类珐琅质“巨型”纤维是弹性枝所特有的;(5)成牙细胞合成并分泌除胶原蛋白外的蛋白到类釉质基质中。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The effects of colchicine on the ultrastructure of odontogenic cells in the common skate, Raja erinacae.

Ultrastructural alterations induced by colchicine were investigated to determine the secretory activities of odontogenic cells during formation of tooth enameloid matrix in skates. Treated skate inner dental epithelial (IDE) cells did not display dilated cisternae of the granular endoplasmic reticulum (GER) nor accumulate Golgi-associated secretory granules at any dose level or time interval examined. This response was markedly different from that observed in teleost IDE cells synthesizing the enameloid collagen matrix. Treated skate IDE cells did show increased accumulations of glycogen-containing vesicles and intercellular glycogen associated with amorphous material, compared to controls. Additionally, the aberrant occurrence of large intracellular glycogen pools and amorphous material suggested that carbohydrate processing was a major function of skate IDE cells. Treated odontoblasts associated with enameloid matrix formation sometimes showed dilated GER cisternae, but procollagen secretory granules were not observed. Instead, electron dense material was present within the Golgi cisternae, tubular granules, and large granules. Some electron-dense material appeared to be shunted to a resorptive pathway via multivesicular bodies in treated odontoblasts. The continuity of tubular granules with the enameloid matrix suggested that they contained precursors of the enameloid matrix, and possibly the periodic, 17.5-nm cross-striated, "giant" fibers. Treated odontoblasts associated with predentin collagen matrix deposition showed dilated GER cisternae and accumulations of procollagen secretory granules, features consistent with the function of active collagen synthesis and secretion. The findings indicate that (1) skate IDE cells do not synthesize enameloid collagen as found in bony fish tooth development; (2) skate IDE cells do process glycogen for secretion into the enameloid matrix; (3) collagen, although present, is not a major constituent of skate enameloid matrix; (4) enameloid "giant" fibers are unique to elasmobranchs; and (5) odontoblasts synthesize and secrete proteins other than collagen into the enameloid matrix.

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