Author
Listed:
- Karen A. DeRocher
(Northwestern University)
- Paul J. M. Smeets
(Northwestern University)
- Berit H. Goodge
(Cornell University
Cornell University)
- Michael J. Zachman
(Cornell University
Oak Ridge National Laboratory)
- Prasanna V. Balachandran
(University of Virginia
University of Virginia)
- Linus Stegbauer
(Northwestern University)
- Michael J. Cohen
(Northwestern University)
- Lyle M. Gordon
(Northwestern University)
- James M. Rondinelli
(Northwestern University)
- Lena F. Kourkoutis
(Cornell University
Cornell University)
- Derk Joester
(Northwestern University)
Abstract
Dental enamel is a principal component of teeth1, and has evolved to bear large chewing forces, resist mechanical fatigue and withstand wear over decades2. Functional impairment and loss of dental enamel, caused by developmental defects or tooth decay (caries), affect health and quality of life, with associated costs to society3. Although the past decade has seen progress in our understanding of enamel formation (amelogenesis) and the functional properties of mature enamel, attempts to repair lesions in this material or to synthesize it in vitro have had limited success4–6. This is partly due to the highly hierarchical structure of enamel and additional complexities arising from chemical gradients7–9. Here we show, using atomic-scale quantitative imaging and correlative spectroscopies, that the nanoscale crystallites of hydroxylapatite (Ca5(PO4)3(OH)), which are the fundamental building blocks of enamel, comprise two nanometric layers enriched in magnesium flanking a core rich in sodium, fluoride and carbonate ions; this sandwich core is surrounded by a shell with lower concentration of substitutional defects. A mechanical model based on density functional theory calculations and X-ray diffraction data predicts that residual stresses arise because of the chemical gradients, in agreement with preferential dissolution of the crystallite core in acidic media. Furthermore, stresses may affect the mechanical resilience of enamel. The two additional layers of hierarchy suggest a possible new model for biological control over crystal growth during amelogenesis, and hint at implications for the preservation of biomarkers during tooth development.
Suggested Citation
Karen A. DeRocher & Paul J. M. Smeets & Berit H. Goodge & Michael J. Zachman & Prasanna V. Balachandran & Linus Stegbauer & Michael J. Cohen & Lyle M. Gordon & James M. Rondinelli & Lena F. Kourkoutis, 2020.
"Chemical gradients in human enamel crystallites,"
Nature, Nature, vol. 583(7814), pages 66-71, July.
Handle:
RePEc:nat:nature:v:583:y:2020:i:7814:d:10.1038_s41586-020-2433-3
DOI: 10.1038/s41586-020-2433-3
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Cited by:
- Jinghua Fang & Xiaozhao Wang & Huinan Lai & Wenyue Li & Xudong Yao & Zongyou Pan & Renwei Mao & Yiyang Yan & Chang Xie & Junxin Lin & Wei Sun & Rui Li & Jiajie Wang & Jiacheng Dai & Kaiwang Xu & Xinni, 2024.
"Decoding the mechanical characteristics of the human anterior cruciate ligament entheses through graduated mineralization interfaces,"
Nature Communications, Nature, vol. 15(1), pages 1-14, December.
- Masternak, Célia & Meunier, Simon & Reinbold, Vincent & Saelens, Dirk & Marchand, Claude & Leroy, Yann, 2024.
"Potential of air-source heat pumps to reduce environmental impacts in 18 European countries,"
Energy, Elsevier, vol. 292(C).
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