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Functional roles of macrophage populations appearing in the renal fibrosis

Functional roles of macrophage populations appearing in the renal fibrosis
巨噬细胞群在肾纤维化中的功能作用
批准号:
12660287
负责人:
YAMATE Jyoji
金额:
$2.56万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2000
资助国家:
日本
项目状态:
已结题
起止时间:
2000 至 2002

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中文摘要
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英文摘要
Macrophagss show heterogeneous functions, consisting of three major types such as exudate macrophages, resident macrophages (histiocytes), and antigen-presenting dendritic cells. This study investigated the properties and participation of macrophage populations in the renal fibrosis.1. Properties of macrophages appearing in chronic renal fibrosis: In the chronic renal fibrosis, that had been induced by repeated injections of cisplatin with nephrotoxicity, exudate and resident macrophages increased at the early stages, and then decreased at the late stages. On the other hand, dendritic cells appeared in greater number at both early and late stages. Because lymphocytes were often present in the late stagss, MHC class II-expressing dendritic cells may be related to induction of lymphocytes.2. Effects of taurine on rat renal fibrosis model: In cisplatin-induced rat renal fibrosis, that had been treated with taurine with antioxidant properties, macrophage numbers were decreased, resulting in reduced fibrosis.3. Characteristics of macrophage populations in thioacetoamide (TAA)-induced rat hepatic fibrosis: In order to compare with macrophagss in renal fibrosis, we investigated lesions of TAA- induced renal fibrosis, with special reference to macrophage populations. In hepatic fibrosis, exudate and resident macrophages, and dendritic cells were present, but there were differences in time points of appearance and distribution between these macrophage populations. In contrast to renal fibrosis, Kupffer cells seemed to play an important role in hepatic fibrosis, and lymphocytes were smaller in number, even though MHC class II-expressing dendritic cells were increased.4. Establishment of in vitro cell model for renal fibrosis: We attempted to establish a cell line (KB-D8) from rat thymus-derived dendritic cell sarcoma. KB-D8 might be useful for studies on dendritic cell nature relating to renal fibrosis.
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Ide, M., et al.: "Emergence of different macrophage populations in hepatic fibrosis following thioacetoamide-induced acute hepatocyte injury in rats."J. Comp. Pathol.. 128(1). 41-51 (2003)
Ide, M., 等人:“硫代乙酰胺诱导大鼠急性肝细胞损伤后肝纤维化中不同巨噬细胞群的出现。”J.
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Yamate, J., et al.: "Establishment and characterization of transplantable tumor line (KB) and cell lines (KB-P and KB-D8) from a rat thymus-derived dendritic cell sarcoma"Virchows Arch.. (In press). (2002)
Yamate, J., 等人:“来自大鼠胸腺源性树突细胞肉瘤的可移植肿瘤系 (KB) 和细胞系(KB-P 和 KB-D8)的建立和表征”Virchows Arch..(出版中)
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Yamate,J., et al.: "Macrophage-like cell line (HS-P) from a rat histiocytic sarcoma"Journal of Comparative Pathology. (in press). (2001)
Yamate, J., et al.:“来自大鼠组织细胞肉瘤的巨噬细胞样细胞系 (HS-P)”比较病理学杂志。
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20
    Pathogenesis of epithelial-mesenchymal transition relating to progressing fibrosis and its clinical significance
    • 批准号:
      23658265
    • 项目类别:
      Grant-in-Aid for Challenging Exploratory Research
    • 资助金额:
      $2.41万
    • 财政年份:
      2011
    • 负责人:
      YAMATE Jyoji
    • 依托单位:
    The pathogenesis of progressive chronic renal disease and therapeutic strategies, based on the axis of macrophages and myofibroblasts
    • 批准号:
      22380173
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $12.31万
    • 财政年份:
      2010
    • 负责人:
      YAMATE Jyoji
    • 依托单位:
    Based on the relationship of macrophages-myofibroblasts, the pathogenesis of renal fibrosis and its therapeutic strategies
    • 批准号:
      18380188
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $11.17万
    • 财政年份:
      2006
    • 负责人:
      YAMATE Jyoji
    • 依托单位:
    Clarification of multi-functions of macrophage populations in renal fibrosis and therapeutic strategies
    • 批准号:
      15380217
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $6.34万
    • 财政年份:
      2003
    • 负责人:
      YAMATE Jyoji
    • 依托单位: