Hou L T, Kollar E J, Yaeger J A
Department of Biostructure and Function School of Dental Medicine, University of Connecticut, Farmington.
J Periodontal Res. 1993 Mar;28(2):102-14. doi: 10.1111/j.1600-0765.1993.tb01057.x.
A model system involving co-cultures of human gingival or periodontal ligament fibroblasts with mouse epithelial root sheath cells or human gingival epithelial cells was used to study epithelial cell-fibroblast interactions. Double-labeled immunofluorescence and microfluorometry were used to investigate the expression of extracellular matrix molecules of collagen type I (collagen I), type III (collagen III) and fibronectin in fibroblasts. When fibroblasts from either source were cultured alone, the fluorescence for collagen I and fibronectin ranged from strongly positive to almost negative. Collagen III staining was relatively weak compared with that of collagen I. After 2-3 days of co-culture, gingival fibroblasts and ligament fibroblasts adjacent to the mouse sheath cells exhibited enhanced intracellular fluorescence for collagen I and fibronectin. Very little change was observed for collagen III. Gingival fibroblasts cultured with gingival epithelial cells showed increased fluorescence for collagen I but decreased fluorescence for fibronectin. In contrast, the fluorescence intensity for both collagen I and fibronectin in ligament fibroblasts were reduced after 3 days of co-culture with gingival epithelial cells. Ultrastructural changes in fibroblasts co-cultured with mouse root sheath cells included increased Golgi cisternae and vesicles and an increased abundance of rough endoplasmic reticulum, polyribosomes, secretory vesicles and pinocytotic vesicles. Thus, the expression of extracellular matrix proteins and the metabolic activity of fibroblasts can be modulated by oral epithelial cells.
一个涉及人牙龈或牙周膜成纤维细胞与小鼠上皮根鞘细胞或人牙龈上皮细胞共培养的模型系统被用于研究上皮细胞与成纤维细胞之间的相互作用。采用双标记免疫荧光和显微荧光测定法来研究成纤维细胞中I型胶原(胶原I)、III型胶原(胶原III)和纤连蛋白等细胞外基质分子的表达。当单独培养来自任何一种来源的成纤维细胞时,胶原I和纤连蛋白的荧光强度范围从强阳性到几乎阴性。与胶原I相比,胶原III染色相对较弱。共培养2 - 3天后,与小鼠鞘细胞相邻的牙龈成纤维细胞和牙周膜成纤维细胞中胶原I和纤连蛋白的细胞内荧光增强。胶原III几乎没有变化。与牙龈上皮细胞共培养的牙龈成纤维细胞显示胶原I荧光增加,但纤连蛋白荧光减少。相反,与牙龈上皮细胞共培养3天后,牙周膜成纤维细胞中胶原I和纤连蛋白的荧光强度均降低。与小鼠根鞘细胞共培养的成纤维细胞的超微结构变化包括高尔基体池和小泡增加,以及粗面内质网、多核糖体、分泌小泡和胞饮小泡的数量增多。因此,口腔上皮细胞可以调节成纤维细胞的细胞外基质蛋白表达和代谢活性。