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Morphological and Immunocytochemical Analyses on the Effects of Diet-induced Hypocalcemia on Enamel Maturation in the Rat Incisor
A. Nancia, P. Mocettia,b, Y. Sakamotoa, M. Kunikataa, E. Lozuponec, and E. Bonucciba Faculté de Médecine Dentaire, Université de Montréal, Montréal, QC, Canada
b Department of Experimental Medicine and Pathology, Università "La Sapienza," Rome, Italy
c Institute of Human Anatomy, University of Bari, Bari, Italy
Correspondence to: A. Nanci, Université de Montréal, Faculty of Dentistry, PO Box 6128, Station Centre-Ville, Montreal, Quebec, Canada H3C 3J7. E-mail: nancia@ere.umontreal.ca
During the maturation stage of amelogenesis, the loss of matrix proteins combined with an accentuated but regulated influx of calcium and phosphate ions into the enamel layer results in the "hardest" tissue of the body. The aim of the present investigation was to examine the effects of chronic hypocalcemia on the maturation of enamel. Twenty-one-day old male Wistar rats were given a calcium-free diet and deionized water for 28 days, while control animals received a normal chow. The rats were perfused with aldehyde and the mandibular incisors were processed for histochemical and ultrastructural analyses and for postembedding colloidal gold immunolabeling with antibodies to amelogenin, ameloblastin, and albumin. The maturation stage enamel organ in hypocalcemic rats exhibited areas with an apparent increase in cell number and the presence of cyst-like structures. In both cases the cells expressed signals for ameloblastin and amelogenin. The content of the cysts was periodic acid–Schiff- and periodic acid–silver nitrate–methanamine-positive and immunolabeled for amelogenin, ameloblastin, and albumin. Masses of a similar material were also found at the enamel surface in depressions of the ameloblast layer. In addition, there were accumulations of glycoproteinaceous matrix at the interface between ameloblasts and enamel. In decalcified specimens, the superficial portion of the enamel matrix sometimes exhibited the presence of tubular crystal "ghosts." The basal lamina, normally separating ameloblasts and enamel during the maturation stage, was missing in some areas. Enamel crystals extended within membrane invaginations at the apical surface of ameloblasts in these areas. Immunolabeling for amelogenin, ameloblastin, and albumin over enamel was variable and showed a heterogeneous distribution. In contrast, enamel in control rats exhibited a homogeneous labeling for amelogenin, a concentration of ameloblastin at the surface, and weak reactivity for albumin. These results suggest that diet-induced chronic hypocalcemia interferes with both cellular and extracellular events during enamel maturation. (J Histochem Cytochem 48:1043–1057, 2000)
Key Words: hypocalcemia, amelogenesis, maturation stage, rat, immunocytochemistry, amelogenin, ameloblastin, albumin
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