A study of the healing mechanisms of destructive periapical lesions and regenerative medicine for periapical bone defect
A study of the healing mechanisms of destructive periapical lesions and regenerative medicine for periapical bone defect
批准号:
16209056
负责人:
ANAN Hisashi
金额:
$30.12万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (A)
财政年份:
2004
资助国家:
日本
项目状态:
已结题
起止时间:
2004 至 2006
中文摘要
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英文摘要
It has been reported that there are three key factors, such as cells, scaffolds and signaling molecules (growth factors), in the regenerative medicine. However, regenerative mechanisms of large-size defects in periapical lesions are not yet well understood. This study presented herein was therefore undertaken to define the progression and healing mechanisms in periapical lesions, and the effects of regenerative materials was investigated. It was showed that transplanted proliferating tissue produced by GTR membrane promoted the formation of new periodontal ligament(PDL) around the tooth. We have established three immortal human PDL fibroblast line by transfecting SV40T-Ag and hTERT into primary PDL fibroblasts.These immortalized cells was useful models for elucidating the biological features and regenerative mechanisms of human PDL. Mineral Trioxide Aggregate could up-regulated osteopontin and osteocalcin mRNA in human PDL to induce their differentiation. FGF-2 enhanced hyaluronan prod … More uction by both human dental pulp cell and human PDL cell and hyaluronan synthase (HAS)1 and HAS2mRNA expression in both cells. Immune and nervous systems play key roles in periapical pathosis, and functional interactions between antigen-presenting cells and nerve fibers may play some roles in the development of self-defense reactions in periapical lesions. In addition, expression of RANKL is correlated with periapical lesion expansion, and followed by the expressions of RANK and OPG. Platelet-rich plasma (PRP) and washed platelets were potent inhibitors of RANKL-induced osteoclast differentiation in RAW264.7 cells. After application of Emdogain containing enamel matrix protein to the root surface, the formation of new cementum and more remarkable recovery of the bone tissue were observed. Although the expression of cytokines, such as IL-1β, RANKL, and RANK were hardly seen, BMP-2and BMP-4 expressing macrophages were increased. It was suggested that wound healing macrophages may express BMP and play an important role in the regeneration of periodontal tissue at the apex in EMD application. Less
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Microflora profiling of root canal utilizing real-time PCR and cloning sequence analysis based 16S rRNA genes-Deference between before and after root canal treatments-
利用实时 PCR 和基于 16S rRNA 基因的克隆序列分析进行根管微生物区系分析-根管治疗前后的差异-
DOI:
--
发表时间:
2007
期刊:
The Japanese Journal of Conservative Dentistry 50(in press)
影响因子:
--
作者:
[Yasuhiro Ito, Takichi Sato, Gen Mayanagi, Keiko Yamaki, Nobuhiro Takahashi, Hidetoshi Shimauchi]
通讯作者:
Hidetoshi Shimauchi
歯根穿孔に由来する歯内-歯周疾患に類似した病変の1症例
牙根穿孔引起的类似牙髓-牙周病的病变一例
DOI:
--
发表时间:
2005
期刊:
日本歯科保存学雑誌 47
影响因子:
--
作者:
[生水真紀夫, 山澤功二, 三橋暁, 確井宏和, 木原真紀, 阿南 壽]
通讯作者:
阿南 壽
A case of lesion mimicking endodontic-periodontal disease caused by crestal root perforation
牙槽嵴根穿孔引起的类似牙髓-牙周病的病变一例
DOI:
--
发表时间:
2005
期刊:
The Japanese Journal of Conservative Dentistry 48(1)
影响因子:
--
作者:
[Anan Hisashi, Nakanishi Miho, Matsumoto Akiko, Yoneda Masahiro, Kimura Ryusei, Kabashima Hiroaki, maeda Katsumasa]
通讯作者:
maeda Katsumasa
Pathological aspects of pulpal and periapical inflammation in Essential Endodontology
基础牙髓病学中牙髓和根尖周炎症的病理学方面
DOI:
--
发表时间:
2007
期刊:
影响因子:
--
作者:
[林田賢史, 今中雄一, 桑原一彰, 他., Mizuki N, 生水真紀夫, 越智光夫, Kawashima N]
通讯作者:
Kawashima N
Kinetic study of immunohistochemical colocalization of antigen presenting cells and nerve fibers in rat periapical lesions.
大鼠根尖周病变中抗原呈递细胞和神经纤维的免疫组织化学共定位的动力学研究。
DOI:
--
发表时间:
2007
期刊:
Journal of Endodontics 33(2)
影响因子:
--
作者:
[Yang G, Kawashima N, Kaneko T, Suzuki N, Okiji T, Suda H]
通讯作者:
Suda H
共 14 条
Development of regenerative medicine for periapical bone defect using a combination of bioactive glass and bone regeneration-stimulating factor
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批准号:24592890
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$3.33万
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财政年份:2012
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负责人:ANAN Hisashi
-
依托单位:
Development of regenerative medicine for periapical bone defect
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批准号:21592439
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$3.0万
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财政年份:2009
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负责人:ANAN Hisashi
-
依托单位:
Development of regenerative medicine for periapical bone defect using bone regeneration-stimulating factors
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批准号:19592219
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.91万
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财政年份:2007
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负责人:ANAN Hisashi
-
依托单位:
An immunohistochemical study of the relationship between periodontopathogens and focal infection
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批准号:12671854
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.24万
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财政年份:2000
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负责人:ANAN Hisashi
-
依托单位:
Expression of IL-1 and adhesion molecules during osteoclast development in rat periapical lesions
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批准号:08672198
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$1.28万
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财政年份:1996
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负责人:ANAN Hisashi
-
依托单位:
A Histopathological Study on the Effect of Indomethacin on Bone Resorption in an Experimental Apical Periodontitis
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批准号:62570857
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项目类别:Grant-in-Aid for General Scientific Research (C)
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资助金额:$1.34万
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财政年份:1987
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负责人:ANAN Hisashi
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依托单位:
海外基金