Abstract
The present study describes a method using immunohistochemical labeling in combination with high-resolution imaging (field emission scanning electron microscopy) to investigate the spatial localization of amelogenins on apatite crystallites in developing porcine enamel. Cross-sections of developing enamel tissue from freeze-fractured pig third molar were treated with antiserum against recombinant mouse amelogenin and immunoreactivity confirmed by Western blot analysis. The samples were then treated with the goat anti-rabbit IgG conjugated with 10-nm gold particles. The control samples were treated with the secondary antibody only. The in-lens secondary electrons detector and quadrant back-scattering detector were employed to reveal the high-resolution morphology of enamel structures and gold particle distribution. The immunolabeling showed a preference of the gold particle localization along the side faces of the ribbon-like apatite crystals. The preferential localization of amelogenin in vivo on enamel crystals strongly supports its direct function in controlling crystal morphology. Copyright © 2008 S. Karger AG.
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Du, C., Fan, D., Sun, Z., Fan, Y., Lakshminarayanan, R., & Moradian-Oldak, J. (2008). Immunogold labeling of amelogenin in developing porcine enamel revealed by field emission scanning electron microscopy. In Cells Tissues Organs (Vol. 189, pp. 207–211). https://doi.org/10.1159/000151385
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