牙硬组织矿化的分子机制。

Current opinion in dentistry Pub Date : 1991-12-01
H Limeback
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引用次数: 0

摘要

在本期报道期间,在牙硬组织生物学领域发表了500多篇论文。这篇综述仅限于那些被认为在牙本质、牙骨质和牙釉质形成中起重要作用的有机基质成分的出版物。在这一领域,基于胶原蛋白的牙齿硬组织(牙本质和牙骨质)的进展主要是在分离和部分表征非胶原蛋白,如蛋白聚糖、磷蛋白和通常在骨骼中发现的蛋白质。这些蛋白被研究是因为它们在指导羟基磷灰石成核或晶体生长方面的潜在作用。牙釉质领域取得的进展主要集中在分子生物学领域。牙釉质在物理上与牙本质和牙骨质有很大的不同,因为它是由非胶原基质(主要是淀粉原蛋白)形成的,它几乎完全被去除,取而代之的是羟基磷灰石。现在在包括牙釉质在内的所有牙齿硬组织中都发现了血清蛋白。对这些进展的临床意义提出了自己的看法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Molecular mechanisms in dental hard tissue mineralization.

During the period covered by this issue, over 500 papers were published in the area of biology of dental hard tissues. This review is limited to publications that focus on the organic matrix components believed to be important in the formation of dentin, cementum, and enamel. The advances made in this area for the collagen-based dental hard tissues (dentin and cementum) have been primarily in the isolation and partial characterization of the noncollagenous proteins such as proteoglycans, phosphoproteins, and proteins normally found in bone. These proteins are being studied because of their potential role for directing hydroxyapatite nucleation or crystal growth. The progress made in the enamel field has been primarily in the area of molecular biology. Enamel is quite different physically from dentin and cementum because it is formed from a noncollagenous matrix (mostly amelogenin), which is almost completely removed and replaced with hydroxyapatite. Serum proteins have now been found in all dental hard tissues including enamel. Opinions on the clinical significance of these advances are provided.

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