Duverger Olivier, Beniash Elia, Morasso Maria I
Laboratory of Skin Biology, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, United States.
Department of Oral Biology, Center for Craniofacial Regeneration, University of Pittsburgh School of Dental Medicine, Pittsburgh, PA, United States; Department of Bioengineering, University of Pittsburgh Swanson School of Engineering, Pittsburgh, PA, United States; McGowan Institute for Regenerative Medicine, Pittsburgh, PA, United States.
Matrix Biol. 2016 May-Jul;52-54:260-265. doi: 10.1016/j.matbio.2015.12.007. Epub 2015 Dec 17.
Dental enamel is the hardest tissue in the human body, and although it starts as a tissue rich in proteins, by the time of eruption of the tooth in the oral cavity only a small fraction of the protein remains. While this organic matrix of enamel represents less than 1% by weight it plays essential roles in improving both toughness and resilience to chemical attacks. Despite the fact that the first studies of the enamel matrix began in the 19th century, its exact composition and mechanisms of its function remain poorly understood. It was proposed that keratin or a keratin-like primitive epithelial component exists in mature enamel, however due to the extreme insolubility of its organic matrix the presence of keratins there was never clearly established. We have recently identified expression of a number of hair keratins in ameloblasts, the enamel secreting cells, and demonstrated their incorporation into mature enamel. Mutation in epithelial hair keratin KRT75 leads to a skin condition called pseudofollicularis barbae. Carriers of this mutation have an altered enamel structure and mechanical properties. Importantly, these individuals have a much higher prevalence of caries. To the best of our knowledge, this is the first study showing a direct link between a mutation in a protein-coding region of a gene and increased caries rates. In this paper we present an overview of the evidence of keratin-like material in enamel that has accumulated over the last 150years. Furthermore, we propose potential mechanisms of action of KTR75 in enamel and highlight the clinical implications of the link between mutations in KRT75 and caries. Finally, we discuss the potential use of keratins for enamel repair.
牙釉质是人体中最坚硬的组织,尽管它最初是一种富含蛋白质的组织,但在牙齿萌出到口腔时,仅剩下一小部分蛋白质。虽然牙釉质的这种有机基质重量占比不到1%,但它在提高韧性和抗化学侵蚀能力方面发挥着重要作用。尽管对牙釉质基质的首次研究始于19世纪,但其确切组成和功能机制仍知之甚少。有人提出成熟牙釉质中存在角蛋白或类似角蛋白的原始上皮成分,然而由于其有机基质的极端不溶性,角蛋白在那里的存在从未得到明确证实。我们最近在成釉细胞(即分泌牙釉质的细胞)中发现了多种毛发角蛋白的表达,并证明它们被整合到成熟牙釉质中。上皮毛发角蛋白KRT75的突变会导致一种名为须假性毛囊角化病的皮肤病。这种突变的携带者牙釉质结构和机械性能发生改变。重要的是,这些个体患龋齿的几率要高得多。据我们所知,这是第一项表明基因蛋白质编码区突变与龋齿率增加之间存在直接联系的研究。在本文中,我们概述了过去150年来积累的关于牙釉质中类角蛋白物质的证据。此外,我们提出了KTR75在牙釉质中的潜在作用机制,并强调了KRT75突变与龋齿之间联系的临床意义。最后,我们讨论了角蛋白在牙釉质修复中的潜在用途。