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牙周膜上皮细胞的多层培养:一种结合上皮模型

Multilayer culture of periodontal ligament epithelial cells: a model for junctional epithelium.

作者信息

Pan Y M, Firth J D, Salonen J I, Uitto V J

机构信息

Department of Oral Biology, University of British Columbia, Vancouver, Canada.

出版信息

J Periodontal Res. 1995 Mar;30(2):97-107. doi: 10.1111/j.1600-0765.1995.tb01258.x.

Abstract

The unique features of junctional epithelium involve lack of keratinization, limited differentiation and a relatively permeable structure. In order to study the relationship between differentiation and permeability of stratified epithelium a model system was developed. Porcine periodontal ligament epithelial cells were cultured on the polycarbonate nucleopore membrane of the Transwell two-compartment culture system. Within 5 days of culture the cells formed a confluent multilayered structure. Subsequently, maturation of the structure and differentiation of surface cells took place. Transmission electron microscopy showed that the cells were arranged into basal and suprabasal layers with sparse desmosomal attachments and wide intercellular spaces resembling the organization of junctional epithelium. The basal cells attached to a subepithelial basal lamina through numerous hemidesmosomes. The cytokeratin profile of the cultured epithelium (K5, 6, 14, 16, 19) resembled that of the cells of junctional epithelium attached to the tooth surface. The older cultures expressed differentiation markers, K4, K13 and involucrin, thereby resembling sulcular epithelium. The epithelial permeability, measured by diffusion of phenol red, radioactive dextran or methionine tracers, and as transepithelial electrical resistance, decreased with the increased cell number and maturation of the cultures. The new model provides an organotypic culture system which allows to control differentiation of a multilayered periodontal epithelium. It thus may serve as a valuable new tool for studies on the permeability and behaviour of periodontal epithelium under the influence of exogenous and endogenous factors.

摘要

结合上皮的独特特征包括缺乏角化、分化有限以及结构相对通透。为了研究复层上皮分化与通透性之间的关系,开发了一种模型系统。将猪牙周膜上皮细胞培养在Transwell双室培养系统的聚碳酸酯核孔膜上。培养5天内,细胞形成汇合的多层结构。随后,结构成熟且表面细胞发生分化。透射电子显微镜显示,细胞排列成基底层和基底上层,桥粒连接稀疏,细胞间隙宽,类似于结合上皮的组织结构。基底细胞通过众多半桥粒附着于上皮下基膜。培养上皮的细胞角蛋白谱(K5、6、14、16、19)与附着于牙面的结合上皮细胞相似。较老的培养物表达分化标志物K4、K13和内披蛋白,从而类似于龈沟上皮。通过酚红、放射性葡聚糖或甲硫氨酸示踪剂的扩散以及跨上皮电阻测量的上皮通透性,随着细胞数量增加和培养物成熟而降低。该新模型提供了一种器官型培养系统,可用于控制多层牙周上皮的分化。因此,它可能成为研究外源性和内源性因素影响下牙周上皮通透性和行为的有价值的新工具。

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