1986 Fiscal Year Final Research Report Summary
Study on the role of enamel proteins on enamel maturation.
| Project/Area Number |
60570862
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| Research Category |
Grant-in-Aid for General Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Research Field |
Morphological basic dentistry
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| Research Institution | Asahi University, School of Dentistry |
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Principal Investigator |
DOI Yutaka Asahi University, School of Dentistry, 歯学部, 助教授 (40116067)
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| Co-Investigator(Kenkyū-buntansha) |
SHIMOKAWA Hitoyata Tokyo Medical and Dental University, Faculty of Dentistry, 歯学部, 助教授 (80014257)
MORIWAKI Yutaka Asahi University, School of Dentistry, 歯学部, 教授 (90028738)
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| Project Period (FY) |
1985 – 1986
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| Keywords | Enamel Proteins / Amelogenin / Enamelin / Calcification-controlling Proteins / Nuclei Formation / Enamel Maturation / Apatite Crystallinity / Selective Protein |
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| Research Abstract |
Seeded crystal growth of enamel and synthetic apatites in the presence of enamel proteins has shown that higher molecular amelogenin and enamelin proteins play important roles in regulating enamel apatite growth. In the presence of enamelin, decrease in amounts of the highest molecular weight amelogenin used results in acceleration of crystal growth of enamel apatite. This in vitro finding confirms well-established in vivo correlation between the protein loss from the calcifing front and increase in rate of enamel calcification. Reactions carried out in a cylindrical polyacrylate fistula with each side partitioned by 1000m.w.-retention cellulose dialysis membrane through which only calcium and phosphate ion species were suppsed to diffuse in and out clearly suggested that the degree of calcifing solution supersaturation is important in estimating inhibitory activity of enamel proteins. In this system where the degree of supersaturation was maintained approximately constant through reaction by the use of less seed, enamel apatite was shown to grow almost twice the original seed in length after one week at 37゜C and pH 7.40. The presence of enamel proteins inside the fistula retarded the rate of crystal growth. The growth process, however, was essentially the same as in the absence of enamel proteins.
CNBr-cleaved amelogenins tested in the system mentioned above showed less inhibitory activity than the parental amelogenin.
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Research Products
(6 results)
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[Publications] 土井豊,E.D.Eanes,下川仁弥太,奥田令以,泰まゆみ,亀水秀男,後藤隆泰,森脇豊,清水紀子,吉田定宏,西川博之,J.D.Termine: 日本結晶成長学会誌. 12. 82-90 (1985)
Description
「研究成果報告書概要(和文)」より
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[Publications] Y. Doi, E.D. Eanes, H. Shimokawa, R. Okuda, M. Hata, H. Kamemizu, T. Goto, Y. Moriwaki, N. Shimizu, S. Yoshida, H. Nishikawa and J.D. Termine: "The effects of enamelo proteins,dentine phosphoproteins, and bone collagene on the seeded crystal growth of enamel apatite and the formation of amorphous calcium phosphate." Jap. J. Cryst. Growth. 12. 82-90 (1985)
Description
「研究成果報告書概要(欧文)」より
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