Manuel P. Mark , Vera Karcher-Djuricic , John R. Baker , Jean-Victor Ruch
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引用次数: 30
摘要
小鼠胚胎磨牙生长在半固体培养基中,培养基中添加了2 mM的β-d-木pyranoside (β-xyloside),这是一种特异性的蛋白聚糖合成抑制剂。细胞外基质中诱导的糖胺聚糖耗竭采用免疫组织化学方法,采用硫酸软骨素4-和硫酸软骨素6-单克隆抗体监测。β-木糖苷抑制牙钟的形成,延缓第一代成牙细胞的出现。成牙细胞的功能分化是在基膜中缺乏硫酸软骨素的情况下进行的。β-木糖苷存在时分泌的Predentin触发成釉细胞的极化,但不允许维持极化的成牙细胞。这些结果支持了一种假说,即在牙齿胚芽中,硫酸软骨素蛋白聚糖参与细胞动力学依赖性形态发生的调节(Mark et al., 1990)。分化43,37 - 50)。另一方面,硫酸软骨素可能在成牙细胞终末分化中起作用的可能性被明确排除。
Effects of β-d-xyloside on morphogenesis and cytodifferentiation in cultured embryonic mouse molars
Embryonic mouse molars were grown on a semi-solid medium supplemented with 2 mM β-d-xylopyranoside (β-xyloside), a specific inhibitor of proteoglycan synthesis. The induced glycosaminoglycan depletion in the extracellular matrix was monitored by immunohistochemistry employing monoclonal antibodies to chondroitin 4- and chondroitin 6-sulfates. β-Xyloside inhibited formation of the dental bell and delayed the appearance of the first odontoblasts. Odontoblast functional differentiation proceeded in the absence of chondroitin sulfate in the basement membrane. Predentin secreted in the presence of β-xyloside triggered the polarization of ameloblasts, but did not allow the maintenance of polarized odontoblasts. These results support the hypothesis that, in the tooth germ, chondroitin sulfate proteoglycans participate in the regulation of cell kinetic-dependent morphogenesis (Mark et al., 1990. Differentiation 43, 37–50). On the other hand, the possibility that chondroitin sulfate might play a role in odontoblast terminal differentiation is definitively ruled out.