Sawada Takashi, Yamazaki Takaki, Shibayama Kazuko, Kumazawa Kaido, Yamaguchi Yoko, Ohshima Mitsuhiro
Department of Ultrastructural Science, Tokyo Dental College, Misaki-cho 2-9-18, Chiyoda-ku, Tokyo, 101-0061, Japan,
J Mol Histol. 2014 Jun;45(3):293-302. doi: 10.1007/s10735-013-9559-7. Epub 2013 Dec 12.
The biochemical composition of the internal and external basal laminae in the junctional epithelium differs significantly, and the precise cellular origin of their respective molecules remains to be determined. In the present study, the expression and localization of three basement membrane-specific molecules-laminin 5 (γ2 chain), type IV collagen (α1 chain), and laminin 10 (α5 chain)-and one tooth-specific molecule, amelotin, was analyzed in adult murine gingiva by using in situ hybridization and immunohistochemistry. The results showed that the outermost cells in junctional epithelium facing the tooth enamel strongly expressed laminin 5 mRNA, supporting the immunohistochemical staining data. This suggests that laminin 5 is actively synthesized in junctional epithelial cells and that the products are incorporated into the internal basal lamina to maintain firm epithelial adhesion to the tooth enamel throughout life. Conversely, no amelotin mRNA signals were detected in the junctional epithelial cells, suggesting that the molecules localized on the internal basal lamina are mainly derived from maturation-stage ameloblasts. Weak and sporadic expression of type IV collagen in addition to laminin 10 in the gingiva indicates that these molecules undergo turnover less frequently in adult animals.
