课题基金 / 基金详情

Functional analysis of neutrophils that infiltrated in the S.mansoni-induced hepatic granuloma

Functional analysis of neutrophils that infiltrated in the S.mansoni-induced hepatic granuloma
曼氏沙门氏菌诱导的肝肉芽肿中浸润的中性粒细胞的功能分析
批准号:
14570211
负责人:
ASAO Hironobu
金额:
$2.24万
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:
2002
资助国家:
日本
项目状态:
已结题
起止时间:
2002 至 2003

项目摘要

项目成果

ASAO Hironobu的其他基金

相似基金

相关文献

中文摘要
翻译
点击翻译按钮获取中文摘要
英文摘要
Schistosomiasis mansoni is a chronic disease progressed after S.mansoni infection. S.mansoni is parasitic in the portal vein. The eggs produced by adult worms are embolized in the hepatic capillary blood vessels and then they form hepatic granulomas. Furthermore it progresses to liver cirrhosis finally. Neutrophils are supposed to have an important role for the hepatic granuloma formation. Then we employed mouse animal model of S.mansoni infection and neutrophil eliminating antibody to examine the functional role of neutrophil on the granuloma formation. 60 cercarias were infected in BALB/c mice intraperitoneally. Before infection or 7 weeks after infection just before egg production from adult worms, mice were injected with rat monoclonal antibody (RB6-8C5) to eliminate neutrophils. 8 or 9 weeks after infection, mouse liver was examined for histophathological examination and TNF-α production or the number of adult worms and eggs in infected mouse feces were checked. Though RB6-8C5 injections reduced the number of peripheral neutrophils dramatically but transiently, the size of formed hepatic granuloma, cells infiltrated in the granuloma, TNF-α production and the number of adult worms and eggs in the feces were not affected in the neutrophil eliminated mice as compared with control antibody injected mice. The transient elimination of neutrophils may not be sufficient to affect the granuloma formation and S.mansoni growth. We need further examinations with different doses and durations of antibody injection to remove neutrophil more completely.
期刊论文(17)
专著(0)
科研奖励(0)
会议论文
Morita E et al.: "Human parvovirus B19 non-structural protein (NS1) induces cell cycle arrest at G1 phase."J.Virol.. 77. 2915-2921 (2003)
Morita E 等人:“人类细小病毒 B19 非结构蛋白 (NS1) 诱导细胞周期停滞在 G1 期。”J.Virol.. 77. 2915-2921 (2003)
DOI: --
发表时间:
期刊:
影响因子: --
作者: []
通讯作者:
Asao H: "Mechanism of Interleukin 2-induced Siganal Transduction"Yamagata Med.J. 21. 141-154 (2003)
Asao H:“白细胞介素2诱导信号转导的机制”Yamagata Med.J。
DOI: --
发表时间:
期刊:
影响因子: --
作者: []
通讯作者:
Morita E: "Human parvovirus B19 non-structural protein (NS1) induces cell cycle arrest at G1 phase."J.Virol.. 77. 2915-2921 (2003)
Morita E:“人类细小病毒 B19 非结构蛋白 (NS1) 诱导细胞周期停滞在 G1 期。”J.Virol.. 77. 2915-2921 (2003)
DOI: --
发表时间:
期刊:
影响因子: --
作者: []
通讯作者:
Kikuchi K et al.: "Identification of AMSH-LP containing a Jab1/MPN domain metalloenzyme motif."Biochem.Biophys.Res.Commun.. 306. 637-643 (2003)
Kikuchi K 等人:“含有 Jab1/MPN 结构域金属酶基序的 AMSH-LP 的鉴定。”Biochem.Biophys.Res.Commun.. 306. 637-643 (2003)
DOI: --
发表时间:
期刊:
影响因子: --
作者: []
通讯作者:
8
    Enhancement of anti-tumor immunity with membrane-bound interleukin 12 (IL-12)
    • 批准号:
      18K07163
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $2.83万
    • 财政年份:
      2018
    • 负责人:
      ASAO Hironobu
    • 依托单位:
    TH17 cell induction through IL-21-Ape1/Ref-1 pathway
    • 批准号:
      22590432
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $2.5万
    • 财政年份:
      2010
    • 负责人:
      ASAO Hironobu
    • 依托单位:
    Grf40, A Novel Grb2 Family Member, Is Involved in T Cell Signaling
    • 批准号:
      11670310
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $2.37万
    • 财政年份:
      1999
    • 负责人:
      ASAO Hironobu
    • 依托单位:
    国内基金
    海外基金
    Mettl3/Syk/MAPK通路调控中性粒细胞胞 外诱捕网 (neutrophil extracellular traps, NETs)的形成对脓毒症急性肺损 伤影响的分子机制研究
    • 批准号:
    • 项目类别:
      省市级项目
    • 资助金额:
      10.0万元
    • 批准年份:
      2025
    • 负责人:
      罗舒华
    • 依托单位:
    骨髓ISG+NAMPT+中性粒细胞介导抗磷脂综合征B细胞异常活化的机制研究
    • 批准号:
      82371799
    • 项目类别:
      面上项目
    • 资助金额:
      47.00万元
    • 批准年份:
      2023
    • 负责人:
      杨程德
    • 依托单位:
    IFITM1+ IL1RAP+ neutrophil通过调控巨噬细胞表型转换驱动ALPPS肝再生的机制研究
    • 批准号:
      82370624
    • 项目类别:
      面上项目
    • 资助金额:
      49万元
    • 批准年份:
      2023
    • 负责人:
      吕涛
    • 依托单位:
    基于Neutrophil-DCs-naive T细胞轴研究“脱敏定喘汤”调体治疗中性粒细胞型过敏性哮喘的机制
    • 批准号:
      --
    • 项目类别:
      青年科学基金项目
    • 资助金额:
      30万元
    • 批准年份:
      2022
    • 负责人:
      周玉美
    • 依托单位: