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

被引:6
|
作者
Snead, Malcolm L. [1 ]
机构
[1] Univ So Calif, Hermann Ostrow Sch Dent USC, Ctr Craniofacial Mol Biol, HSC, Los Angeles, CA 90032 USA
关键词
MOUSE AMELOGENIN GENE; BINDING-PROTEIN-ALPHA; MATURATION-STAGE AMELOBLASTS; MOLECULAR-MECHANISMS; IMPERFECTA PHENOTYPE; MINERALIZED TISSUE; MICE DISPLAY; EXPRESSION; EVOLUTION; INCISORS;
D O I
10.1007/s11837-015-1305-z
中图分类号
T [工业技术];
学科分类号
08 ;
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.
引用
收藏
页码:788 / 795
页数:8
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