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Pathogenic mechanisms of apical periodontal diseases : Kinetics of dendritic cells and immure functional molecules

Pathogenic mechanisms of apical periodontal diseases : Kinetics of dendritic cells and immure functional molecules
根尖周病的发病机制:树突状细胞和免疫功能分子的动力学
批准号:
14370616
负责人:
OKIJI Takashi
金额:
$5.95万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B)
财政年份:
2002
资助国家:
日本
项目状态:
已结题
起止时间:
2002 至 2004

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中文摘要
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英文摘要
This study aimed to investigate the role of dendritic cells in the development of apical periodontitis. Experimental periapical lesions were induced in rat molars by making unsealed pulp exposures, and ultrastructure, distributional density and immune functional molecule expression of dendritic cells were investigated by means of inmunoelectron microscopy. During the period of active lesion expansion (expanding stage), macrophages were dominant and only a small number of dendritic cells were detected. Following lesion stabilization (chronic stage), however, most of MHC class II molecule-expressing cells were identified as dendritic cells. Cell-to-cell contact between dendritic cells and lymphocytes was sometimes seen in the chronic stage. Morphological change of dendritic cells was also noted : cells with thin and short cytoplasmic processes and poorly developed organelles were predominant in the expanding stage, whereas large cells with long cytoplasmic processes were predominant in the chronic stage. Moreover, dendritic cells in the chronic stage were divided into two subpopulations according to the immunoreactivity to CD11c and OX62 : although most dendritic cells expressed CD11c, there were minor but definite subpopulation which expressed OX62 and had a small and round cell body with a small number of short cytoplasmic processes. These findings suggested that dendritic cells, composed of different subpopulations according to the stage of maturation/activation, are involved in lesion chronicity by acting as antigen presenting cells in response to chronic antigenic challenge from infected root canals.
期刊论文(48)
专著(0)
科研奖励(0)
会议论文
新編口腔組織発生学
新版口腔组织胚胎学
DOI: --
发表时间: 2005
期刊:
影响因子: --
作者: [Chowdhury SA, Kishino K, Satoh R et al., 興地隆史]
通讯作者: 興地隆史
根尖歯周組織の生体防御・修復機構
根尖牙周组织的生物防御和修复机制
DOI: --
发表时间: 2005
期刊: The Quintessence 24(印刷中)
影响因子: --
作者: [高山直士, 田島雅道, 菊地寛高, 西川博文, 坂上宏ら, 興地隆史]
通讯作者: 興地隆史
興地隆史: "結合素子としての歯髄"The Quintessence. 22. 135-144 (2003)
Takashi Kochi:“牙髓作为连接元素”The Quintessence 22. 135-144 (2003)。
DOI: --
发表时间:
期刊:
影响因子: --
作者: []
通讯作者:
DOI: --
发表时间: 2004
期刊: 日本歯科保存学雑誌 47
影响因子: --
作者: [Lee, J., Adachi, K., Gionhaku, N., Fujita, S., Uchida, T., Gerstner, G.E., Koshikawa, N., 金子友厚]
通讯作者: 金子友厚
15
    An investigation of factors that promote dental pulp regeneration and stem cell differentiation in a rat model of coronal pulp regeneration
    • 批准号:
      17H04380
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $10.98万
    • 财政年份:
      2017
    • 负责人:
      OKIJI Takashi
    • 依托单位:
    Investigation of determining factors for the reparative process of the dentin/pulp complex using a new experimental model
    • 批准号:
      15K15699
    • 项目类别:
      Grant-in-Aid for Challenging Exploratory Research
    • 资助金额:
      $2.25万
    • 财政年份:
      2015
    • 负责人:
      OKIJI Takashi
    • 依托单位:
    Regeneration of rat molar pulp tissue by the implantation of stem cells from incisor pulp: development of a rat model of autologous pulp tissue engineering
    • 批准号:
      26293405
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $10.4万
    • 财政年份:
      2014
    • 负责人:
      OKIJI Takashi
    • 依托单位:
    Application of activated macrophages derived from dental pulp stem cells to dental pulp tissue engineering
    • 批准号:
      25670808
    • 项目类别:
      Grant-in-Aid for Challenging Exploratory Research
    • 资助金额:
      $2.33万
    • 财政年份:
      2013
    • 负责人:
      OKIJI Takashi
    • 依托单位:
    海外基金