A study on the mechanisms of tissue wound healing and regeneration of dental pulp
Project/Area Number |
24592863
|
Research Category |
Grant-in-Aid for Scientific Research (C)
|
Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Conservative dentistry
|
Research Institution | Niigata University |
Principal Investigator |
|
Co-Investigator(Kenkyū-buntansha) |
YOSHIBA Nagako 新潟大学, 医歯学総合病院, 講師 (10323974)
|
Project Period (FY) |
2012-04-01 – 2015-03-31
|
Project Status |
Completed (Fiscal Year 2014)
|
Budget Amount *help |
¥5,200,000 (Direct Cost: ¥4,000,000、Indirect Cost: ¥1,200,000)
Fiscal Year 2014: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2013: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
Fiscal Year 2012: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
|
Keywords | 象牙質・歯髄複合体 / 歯髄組織幹細胞 / 直接覆髄 / 組織培養 / 象牙芽細胞 / 歯髄創傷治癒 / 組織幹細胞 / α-smooth muscle actin / マクロファージ / 窩洞形成 / 歯髄保存療法 / 歯の移植 |
Outline of Final Research Achievements |
The aim of this study was to elucidate cellular events during pulp tissue wound healing and reparative dentin formation after direct pulp capping. M2 macrophage-associated molecule-expressing cells transiently accumulated beneath the exposure site. The deposition of osteopontin and dentin matrix protein 1 (DMP1) at exposed pulp sites preceded the appearance of nestin-immunoreactive cells, active cell proliferation and new matrix formation. These suggest that M2 macrophages participate in the initial phases of the healing and that osteopontin and DMP1 act as a trigger of pulp repair. In addition, numerous α-smooth muscle actin (SMA)-positive cells emerged at the wound margin, and the initially formed mineralized barrier was lined with α-SMA-positive cells similar in appearance to reparative odontoblasts, some of which co-expressed nestin. Fibrillin-1 degradation and down-regulation might be implicated in the differentiation of α-SMA-positive cells in this process.
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Report
(4 results)
Research Products
(55 results)