4.4 Article

Loss of biological control of enamel mineralization in amelogenin-phosphorylation-deficient mice

期刊

JOURNAL OF STRUCTURAL BIOLOGY
卷 214, 期 2, 页码 -

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jsb.2022.107844

关键词

Dental enamel; Amelogenin; Biomineralization; Phosphorylation

资金

  1. National Institutes of Health/National Institute of Dental and Craniofacial Research [R01 DE029211]
  2. DOE-BES-Chemical Sciences, Geosciences, Biosciences-Geosciences [DEFG02-07ER15899]
  3. Laboratory Directed Research and Development (LDRD) program at Berkeley Lab, through DOE-BES [DE-AC0205CH11231]
  4. DOE-BES [DE-AC0205CH11231]
  5. NSF Biomaterials Grant [DMR1603192]
  6. Office of Science, Office of Basic Energy Sciences, US Department of Energy [DE-AC02-05CH11231]

向作者/读者索取更多资源

Amelogenin phosphorylation plays crucial roles in controlling the structural, crystallographic, mechanical, and compositional characteristics of dental enamel.
Amelogenin, the most abundant enamel matrix protein, plays several critical roles in enamel formation. Importantly, we previously found that the singular phosphorylation site at Ser16 in amelogenin plays an essential role in amelogenesis. Studies of genetically knock-in (KI) modified mice in which Ser16 in amelogenin is substituted with Ala that prevents amelogenin phosphorylation, and in vitro mineralization experiments, have shown that phosphorylated amelogenin transiently stabilizes amorphous calcium phosphate (ACP), the initial mineral phase in forming enamel. Furthermore, KI mice exhibit dramatic differences in the enamel structure compared with wild type (WT) mice, including thinner enamel lacking enamel rods and ectopic surface calcifications. Here, we now demonstrate that amelogenin phosphorylation also affects the organization and composition of mature enamel mineral. We compared WT, KI, and heterozygous (HET) enamel and found that in the WT elongated crystals are co-oriented within each rod, however, their c-axes are not aligned with the rods' axes. In contrast, in rod-less KI enamel, crystalline c-axes are less co-oriented, with misorientation progressively increasing toward the enamel surface, which contains spherulites, with a morphology consistent with abiotic formation. Furthermore, we found significant differences in enamel hardness and carbonate content between the genotypes. ACP was also observed in the interrod of WT and HET enamel, and throughout aprismatic KI enamel. In conclusion, amelogenin phosphorylation plays crucial roles in controlling structural, crystallographic, mechanical, and compositional characteristics of dental enamel. Thus, loss of amelogenin phosphorylation leads to a reduction in the biological control over the enamel mineralization process.

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