Breschi L, Gobbi P, Lopes M, Prati C, Falconi M, Teti G, Mazzotti G
Department of Social Sciences, University of Trieste, Trieste, Italy.
J Biomed Mater Res A. 2003 Oct 1;67(1):11-7. doi: 10.1002/jbm.a.10048.
Immunocytochemical analysis is a fundamental and selective technique for identifying different molecular components of human dental structure. The hypothesis tested here is that the application of different etching solutions on dentin does not hinder collagen fibrils and proteoglycans from maintaining their immunochemical antigenicity. Human dentin disks were treated with 0.5M of EDTA, citric acid, maleic acid, or phosphoric acid (for 15 or 30 s). A double-immunolabeling technique was performed to identify, simultaneously, collagen fibrils and chondroitin sulfate. The use of different acids resulted in different degrees of labeling. Maleic and citric acids revealed a diffuse and intense labeling for both collagen fibrils and proteoglycans. The use of phosphoric acid on dentin showed a massive coagulation of the proteoglycans (15 s) or very low labeling (30 s). These data clarify that the use of acids on dentin components is able to modify their antigenicity. Moreover, the double-labeling immunocytochemical technique allows understanding of the spatial relationships between the collagen fibrils and proteoglycans of the dentin matrix.
免疫细胞化学分析是鉴定人类牙齿结构不同分子成分的一项基本且具有选择性的技术。此处所验证的假设是,在牙本质上应用不同的酸蚀剂溶液不会妨碍胶原纤维和蛋白聚糖保持其免疫化学抗原性。将人类牙本质盘用0.5M的乙二胺四乙酸(EDTA)、柠檬酸、马来酸或磷酸处理(15秒或30秒)。采用双重免疫标记技术同时鉴定胶原纤维和硫酸软骨素。使用不同的酸会导致不同程度的标记。马来酸和柠檬酸对胶原纤维和蛋白聚糖均显示出弥漫且强烈的标记。在牙本质上使用磷酸显示出蛋白聚糖大量凝聚(15秒)或标记非常低(30秒)。这些数据表明,在牙本质成分上使用酸能够改变其抗原性。此外,双重标记免疫细胞化学技术有助于了解牙本质基质中胶原纤维和蛋白聚糖之间的空间关系。