Antigenic alterations to the dentin organic matrix may be detected by an immunohistochemical approach. We hypothesized that alterations in the antigenicity of type I collagen and proteoglycans occur in sclerotic dentin under caries lesions. Transverse sections were prepared from carious teeth in the sclerotic zone and normal hard dentin. A double-immunolabeling technique was performed on these sections, with anti-type I collagen and anti-chondroitin 4/6 sulfate monoclonal primary antibodies. We used gold-conjugated secondary antibodies to visualize the distribution of intact collagen fibrils and proteoglycans by high-resolution SEM. For sclerotic dentin, labeling densities were 19.57 +/- 3.01/mu m(2) for collagen and 9.84 +/- 2.62/mu m(2) for proteoglycans. For normal hard dentin, values were 35.20 +/- 2.73/mu m(2) and 17.03 +/- 1.98/mu m(2), respectively. Distribution of intact collagen fibrils and proteoglycans in sclerotic dentin was significantly lower than in normal hard dentin. Reductions in antigenicity from the organic matrix of sclerotic dentin under caries lesions raise concern about the potential of intrafibrillar remineralization.
Suppa P, Ruggeri A jr, Tay FR, Prati C, Biasotto M, Falconi M, et al. (2006). Reduced Antigenicity of type I collagen and proteoglycans in sclerotic dentin. JOURNAL OF DENTAL RESEARCH, 85(2), 133-137.
Reduced Antigenicity of type I collagen and proteoglycans in sclerotic dentin
RUGGERI, ALESSANDRA;PRATI, CARLO;FALCONI, MIRELLA;BRESCHI, LORENZO
2006
Abstract
Antigenic alterations to the dentin organic matrix may be detected by an immunohistochemical approach. We hypothesized that alterations in the antigenicity of type I collagen and proteoglycans occur in sclerotic dentin under caries lesions. Transverse sections were prepared from carious teeth in the sclerotic zone and normal hard dentin. A double-immunolabeling technique was performed on these sections, with anti-type I collagen and anti-chondroitin 4/6 sulfate monoclonal primary antibodies. We used gold-conjugated secondary antibodies to visualize the distribution of intact collagen fibrils and proteoglycans by high-resolution SEM. For sclerotic dentin, labeling densities were 19.57 +/- 3.01/mu m(2) for collagen and 9.84 +/- 2.62/mu m(2) for proteoglycans. For normal hard dentin, values were 35.20 +/- 2.73/mu m(2) and 17.03 +/- 1.98/mu m(2), respectively. Distribution of intact collagen fibrils and proteoglycans in sclerotic dentin was significantly lower than in normal hard dentin. Reductions in antigenicity from the organic matrix of sclerotic dentin under caries lesions raise concern about the potential of intrafibrillar remineralization.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.