Project/Area Number |
17591903
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Morphological basic dentistry
|
Research Institution | Niigata University |
Principal Investigator |
KAWANO Yoshiro Niigata University, Institute of Medicine and Dentistry, Assistant, 医歯学系, 助手 (60303129)
|
Co-Investigator(Kenkyū-buntansha) |
MAEDA Takeyasu Niigata University, Institute of Medicine and Dentistry, Professor, 医歯学系, 教授 (40183941)
AMIZUKA Norio Niigata University, Transdisciplinary Researchiences, Professor, 超域研究機構, 教授 (30242431)
INOUE Kayoko (NOZAWA Kayoko) Niigata University, Institute of Medicine and Dentistry, Associate Professor, 医歯学系, 助教授 (90303130)
|
Project Period (FY) |
2005 – 2006
|
Project Status |
Completed (Fiscal Year 2006)
|
Budget Amount *help |
¥3,500,000 (Direct Cost: ¥3,500,000)
Fiscal Year 2006: ¥1,400,000 (Direct Cost: ¥1,400,000)
Fiscal Year 2005: ¥2,100,000 (Direct Cost: ¥2,100,000)
|
Keywords | epithelio-mesenchymal transformation / S100 / cementblasts / heat shock protein / 器官培養 / 歯根上皮鞘 |
Research Abstract |
It is well known that the epithelial root sheath is greatly involved in the root dentin formation and the development of periodontium. Two possibilities on the fate of epithelial root sheath cells are proposed, the pathway to be extinguished by the apoptosis, and the pathway to transform into cementblasts by epithelio-mesenchymal transformation. Phenotypic transformation from the epithelial cell into the mesenchymal cell is reported in developing Muellerian duct and the epithelial cells in the median palatine suture, and recognized in the transformation from cancer cells into invasive metastatic cells in a pathogenic case. The origin of cementblastic cells remains controversial. Mature cementblasts produce matrix proteins common to osteoblasts, such as Type I collagen, osteocalcin, and osteopontin. These features led to the suggestion that the cementblasts are uniquely positioned osteoblasts. On the other hand, morphological data and the expression in some cementblasts of dental epithel
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ium markers, such as karatin, E-cadherin and amelin/ameloblastion/sheathlin, support the hypothesis that root epithelium-derived cells also persist during cementum formation. These findings support the epithelial-mesenchymal transformation hypothesis that epithelial root sheath cells differentiate into cementoblasts. However, to date, the spatial-temporal behavior of epithelial root sheath cells and its mechanism has not been elucidated. The immunohistochemisty demonstrated that a certain kind of heat shock protein was expressed continuously from the epithelial cells to the cementblasts on the root dentin and that a certain kind of aquapolin and S100 protein were expressed in the cementoblasts in the rat incisor. The expression pattern of these proteins during cementum formation illustrates the complex origin of cementblasts and the fate of epithelial root sheath cells. These results suggest mesenchymal transition in odontogenic epithelium and the importance of these proteins during the cement genesis. Less
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