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人牙釉质和牙骨质上获得性膜成分的体外放射性标记

External radiolabelling of components of pellicle on human enamel and cementum.

作者信息

Fisher S J, Prakobphol A, Kajisa L, Murray P A

机构信息

Division of Oral Biology, School of Dentistry, University of California, San Francisco 94143.

出版信息

Arch Oral Biol. 1987;32(7):509-17. doi: 10.1016/s0003-9969(87)80013-4.

Abstract

Enamel and cementum pellicles form by different adsorption of salivary and serum components to the tooth surface. The authors compared the constituents of surface pellicle formed on human enamel and cementum under three conditions: (1) natural pellicle, present on extracted teeth, which was formed by prolonged exposure to human salivary and serum components in vivo; (2) short-term in-vivo pellicle, formed by exposing enamel and cementum slabs to the oral environment for 0-60 min; (3) in-vivo pellicle, formed by incubating enamel and cementum slabs in a 1:1 mixture of parotid and submandibular/sublingual saliva for 0-60 min. Pellicle composition was characterized by external radiolabelling techniques specific for exposed carbohydrate (sialic acid and galactose) and amino-acid (tyrosine) residues. There were differences between cementum and enamel in the electrophoretic profiles of natural-pellicle components; notably, a major 180 kda 3H-labelled sialoglycoprotein, unique to the cementum pellicle, had the same electrophoretic mobility as the low-molecular-weight mucin from human submandibular/sublingual saliva. After alkaline-borohydride treatment, 3H-labelled natural-pellicle oligosaccharides chromatographed in the di- to tetrasaccharide region of a Bio-Gel P-2 column. The most prominently labelled components of short-term enamel and cementum pellicles in vivo and in vitro had the same electrophoretic mobility as the low-molecular-weight salivary mucin. The pellicle components formed in vitro, unlike those formed for the same period of time in vivo, were rapidly desorbed from the cementum, but not from the enamel surface. We conclude that: (1) external labelling techniques are useful for obtaining a profile of pellicle components; (2) submandibular/salivary mucins are major constituents of salivary pellicles on tooth surfaces; (3) glycoproteins that carry low-molecular-weight, sialic-acid-containing saccharides are important determinants of pellicle surface properties [corrected].

摘要

牙釉质和牙骨质薄膜通过唾液和血清成分在牙齿表面的不同吸附作用而形成。作者比较了在三种条件下在人牙釉质和牙骨质上形成的表面薄膜的成分:(1)天然薄膜,存在于拔除的牙齿上,是通过在体内长时间暴露于人类唾液和血清成分而形成的;(2)短期体内薄膜,通过将牙釉质和牙骨质薄片暴露于口腔环境0 - 60分钟而形成;(3)体内薄膜,通过将牙釉质和牙骨质薄片在腮腺和下颌下腺/舌下腺唾液的1:1混合物中孵育0 - 60分钟而形成。薄膜成分通过针对暴露的碳水化合物(唾液酸和半乳糖)和氨基酸(酪氨酸)残基的外部放射性标记技术进行表征。天然薄膜成分的电泳图谱在牙骨质和牙釉质之间存在差异;值得注意的是,一种主要的180 kDa 3H标记的唾液糖蛋白,是牙骨质薄膜所特有的,其电泳迁移率与来自人下颌下腺/舌下腺唾液的低分子量粘蛋白相同。经过碱性硼氢化处理后,3H标记的天然薄膜寡糖在Bio - Gel P - 2柱的二糖至四糖区域进行色谱分析。体内和体外短期牙釉质和牙骨质薄膜中标记最明显的成分与低分子量唾液粘蛋白具有相同的电泳迁移率。与在体内相同时间段形成的薄膜成分不同,体外形成的薄膜成分能迅速从牙骨质上解吸,但不能从牙釉质表面解吸。我们得出以下结论:(1)外部标记技术有助于获取薄膜成分的概况;(2)下颌下腺/唾液粘蛋白是牙齿表面唾液薄膜的主要成分;(3)携带低分子量、含唾液酸糖类的糖蛋白是薄膜表面性质的重要决定因素[已修正]。

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