Studies on the Candida albicans-tissues interaction in disseminated candidiasis
Studies on the Candida albicans-tissues interaction in disseminated candidiasis
批准号:
09670278
负责人:
KANBE Toshio
金额:
$2.05万
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:
1997
资助国家:
日本
项目状态:
已结题
起止时间:
1997 至 1998
中文摘要
传染病微生物通常以特定的宿主组织为目标,而不是随机入侵器官。弥散性念珠菌病的发病机制的第一步是真菌与宿主组织的粘连。我们采用了一种体外试验来研究白色念珠菌从血液扩散到内脏器官的机制。白念珠菌与小鼠脾的边缘带巨噬细胞特异性结合。白念珠菌细胞壁磷甘露糖苷蛋白复合体(PMPC)的酸性稳定部分均匀地显示在白色念珠菌酵母和菌丝体的细胞表面,PMPC酸性稳定部分的甘露聚糖核心和低聚甘露糖基侧链是该真菌在体外与边缘带巨噬细胞黏附的原因。酵母细胞在体内依赖PMPC与脾边缘带的黏附机制与体外实验中的黏附机制相似,这是因为边缘区巨噬细胞表达甘露糖样受体。最后,我们从J774.E细胞系获得的结果表明,脾边缘区和淋巴组织中的巨噬细胞表达一种MR黏附系统,该黏附系统唯一地结合白色念珠菌酵母细胞。这种相互作用可能在播散性念珠菌病的发病机制中起重要作用。
英文摘要
Infectious disease microorganisms usually target specific host tissues rather than invading organs randomly. An initial step in the pathogenesis of a dissiminated candidiasis is adherence of the fungus to the host tissue. We have adapted an ex vivo assay to study the mechanisms of Candida albicans dissemination from the blood into internal organs. C.albicans binds specifically to the marginal zone macmrophages of mouse spleen. The acid-stable part of C.albicans cell wall phosphomannoprotein complex (PMPC) displayed homogenously on the C.albicans yeast and hyphal form cell surface, and both mannan core and oligomannosyl side chains of the acid-stable part of PMPC are responsible for the adherence of this fungus to the marginal zone macrophages ex vivo. The in vivo PMPC-dependent adherence of yeast cells to the splenic marginal zone occurs by a similar mechanism as adherence in the ex vivo assay, which is because of a mannose-like receptor expressed by mmarginal zone macrophages. Finally, our results obtained from J774.E cell line suggest that macrophages in the splenic marginal zone and lymph node tissues express a MR adhesion system that uniquely binds C.albicans yeast cells. This interaction may be important in the pathogenesis of disseminated candidiasis.
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T.Kawagoe et al.: "Measurement of (1→3)-β-D-glucan in an experimental model of systemic candidiasis." Eur.Surg.Res.30. 290-296 (1998)
T.Kawagoe 等人:“系统性念珠菌病实验模型中 (1→3)-β-D-葡聚糖的测量。”Eur.Surg.Res.30 (1998)。
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通讯作者:
T.Kanbe and J.E.Cutler: "Minimum chemical requirements for adhesin activity of the acid-stable part of the Candida albicans cell wall phosphomannoprotein complex(PMPC)." Infect.and Immun.66・12. 5812-5818 (1998)
T.Kanbe 和 J.E.Cutler:“白色念珠菌细胞壁磷酸甘露糖蛋白复合物 (PMPC) 的酸稳定部分的粘附素活性的最低化学要求。Infect.and Immun.5812-5818 (1998)”
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Y.Han et al.: "Biochemical characterization of Candida albicans epitopes that can elicit protective and nonprotective antibodies." Infect.and Immun.65・10. 4100-4107 (1997)
Y.Han 等人:“可引发保护性和非保护性抗体的白色念珠菌表位的生化特征。Infect.and Immun.65·10 (1997)”
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Han, Y.et al.: "Biochemical characterization of Candida albicans epitopes that can elicit protectiveand nonprotective antibodies." Infect.Immun.65. 4100-4107 (1997)
Han, Y. 等人:“可引发保护性和非保护性抗体的白色念珠菌表位的生化特征。”
DOI:
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发表时间:
期刊:
影响因子:
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作者:
[]
通讯作者:
T.Kawagoe et al.: "Measurement of(1→3)-β-D-glucan in an experimental model of systemic candidiasis." Eur.Surg.Res.30. 290-296 (1998)
T. Kawagoe 等人:“系统性念珠菌病实验模型中 (1→3)-β-D-葡聚糖的测量。”Eur.Surg.Res.30 (1998)。
DOI:
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共 9 条
Strain typing of Candida alhiranstargeting to repeat sequences in each chromosome
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批准号:18590418
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.45万
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财政年份:2006
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负责人:KANBE Toshio
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依托单位:
Nucletide sequencing of DNA topoisomerase II gene for diagnosis of fungal infection
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批准号:11670262
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.3万
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财政年份:1999
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负责人:KANBE Toshio
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依托单位:
海外基金