Biomineralization of a Self-assembled, Soft-Matrix Precursor: Enamel

被引:0
作者
Malcolm L. Snead
机构
[1] University of Southern California,Center for Craniofacial Molecular Biology, Hermann Ostrow School of Dentistry of USC
来源
JOM | 2015年 / 67卷
关键词
Enamel Matrix; Amelogenesis Imperfecta; Enamel Formation; Enamel Protein; Amelogenin Gene;
D O I
暂无
中图分类号
学科分类号
摘要
Enamel is the bioceramic covering of teeth, a composite tissue composed of hierarchical organized hydroxyapatite crystallites fabricated by cells under physiologic pH and temperature. Enamel material properties resist wear and fracture to serve a lifetime of chewing. Understanding the cellular and molecular mechanisms for enamel formation may allow a biology-inspired approach to material fabrication based on self-assembling proteins that control form and function. A genetic understanding of human diseases exposes insight from nature’s errors by exposing critical fabrication events that can be validated experimentally and duplicated in mice using genetic engineering to phenocopy the human disease so that it can be explored in detail. This approach led to an assessment of amelogenin protein self-assembly that, when altered, disrupts fabrication of the soft enamel protein matrix. A misassembled protein matrix precursor results in loss of cell-to-matrix contacts essential to fabrication and mineralization.
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页码:788 / 795
页数:7
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