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Infecton Mechanisms of Malarail Parasite Sporozoites to the Liver Cells

Infecton Mechanisms of Malarail Parasite Sporozoites to the Liver Cells
Malarail寄生虫子孢子对肝细胞的感染机制
批准号:
16017243
负责人:
CHINZEI Yasuo
金额:
$9.6万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research on Priority Areas
财政年份:
2004
资助国家:
日本
项目状态:
已结题
起止时间:
2004 至 2005

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中文摘要
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英文摘要
Malarial parasites have very complicated life cycle. There are many steps for the parasites to invade into the host tissues or cells of both vector mosquito and vertebrate animal. We are interested in molecular mechanisms of the parasite invasion of host tissues. We have analyzed parasite proteins essential for invasion into host mosquito midgut and host liver using the rodent malaria Plasmodium berghei. We established EST (expressed sequence tags) databases of ookinetes and sporozoites, selected some molecules based on certain criteria, and analyzed their function by gene targeting disruption. We have elucidated several molecules that function in parasite infection (movement, recognition, invasion, development and/or proliferation) of host. We identifiedand and named as CTRP (CS TRAP Related Protein) and MAOP (Membrane Attack Ookinete Protein) from sporozoite and ookinete stages of parasites. Both proteins have membrane attack complex /perforin domain in the molecule and function to rupture the cell membrane of Kuppfer cell in the liver sinusoidal layer and mosquito midgut cell respectively. Ookinetes and sporozoites have cellular barriers, midgut epithelial cells of mosquitoes for ookinetes and the sinusoidal layer cells in the liver for sporozoites to reach their respective infective sites. Malarial parasites use different homologous molecules, and a common conserved cell traversal
期刊论文(26)
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会议论文
Plasmodium sporozoite micronemal protein with a membrane attack complex-related domain is required for breaching the liver sinusoidal cell layer prior to hepatocyte infection.
具有膜攻击复合物相关结构域的疟原虫子孢子微线蛋白是在肝细胞感染之前突破肝窦细胞层所必需的。
DOI: --
发表时间: 2005
期刊: Cell. Microbiol. 7
影响因子: --
作者: [Tomoko Ishino, Yasuo Chinzei, Masao YudaA]
通讯作者: Masao YudaA
DOI: 10.1111/j.1365-2958.2005.04801.x
发表时间: 2005-12-01
期刊: MOLECULAR MICROBIOLOGY
影响因子: 3.6
作者: [Ishino, T, Chinzei, Y, Yuda, M]
通讯作者: Yuda, M
(* : equally contributed) CelTOS, a novel malarial protein that mediates transmission to mosquito and vertebrate hosts.
(*:同等贡献)CelTOS,一种新型疟疾蛋白,可介导向蚊子和脊椎动物宿主的传播。
DOI: --
发表时间: 2006
期刊: Mol.Microbiol. 59
影响因子: --
作者: [Tohru Kariu*, Tomoko Ishino*, Kazuhisa Yano, Yasuo Chinzei, Masao Yuda.]
通讯作者: Masao Yuda.
Two proteins with 6-cys motifs are required for malarial parasites to commit to infection of the hepatocyte.Mol.
疟疾寄生虫需要两种具有 6-cys 基序的蛋白质来感染肝细胞。
DOI: --
发表时间: 2005
期刊: Microbiol 58
影响因子: --
作者: [Tomoko Ishino, Yasuo Chinzei, Masao Yuda]
通讯作者: Masao Yuda
8
    Malarial parasite molecules essential for development from sporoziote to merozoite in the liver stage.
    • 批准号:
      21590472
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $2.91万
    • 财政年份:
      2009
    • 负责人:
      CHINZEI Yasuo
    • 依托单位:
    Studies on the Mechanisms of Stage specific Host Infection in Malarial Parasite
    Sage specific host cell infection mechanism of malarial parasite
    • 批准号:
      14207011
    • 项目类别:
      Grant-in-Aid for Scientific Research (A)
    • 资助金额:
      $28.12万
    • 财政年份:
      2002
    • 负责人:
      CHINZEI Yasuo
    • 依托单位:
    Function and Structure Analyses of Anticoagulant and Vasodilator Isolated from the Salivary Glands of Blood Sucking Insects, and Development of Novel Medicine
    • 批准号:
      11557022
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $8.64万
    • 财政年份:
      1999
    • 负责人:
      CHINZEI Yasuo
    • 依托单位:
    海外基金