Nishikawa S, Tsukita S, Tsukita S, Sasa S
Department of Histology, Kanagawa Dental College, Japan.
Cell Struct Funct. 1990 Oct;15(5):245-9. doi: 10.1247/csf.15.245.
Localization of junctions between inner enamel-secretory ameloblasts was examined by immunofluorescence microscopy using antibodies against adherens junction proteins, radixin, vinculin, and A-CAM. All antibodies used stained the boundary between the ameloblasts exclusively in the plane where F-actin was abundant. This suggests that the adherens junctions in the ameloblasts are involved in cell-to-cell movement with actin-based microfilament bundles.
利用针对黏着连接蛋白、根蛋白、纽蛋白和A-CAM的抗体，通过免疫荧光显微镜检查内釉质分泌成釉细胞之间连接的定位。所有使用的抗体仅在F-肌动蛋白丰富的平面上染成釉细胞之间的边界。这表明成釉细胞中的黏着连接与基于肌动蛋白的微丝束的细胞间移动有关。
