Functional analyses of esophageal glands of parasitic nematodes

寄生线虫食管腺的功能分析

基本信息

  • 批准号:
    15590372
  • 负责人:
  • 金额:
    $ 2.3万
  • 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:
    2003
  • 资助国家:
    日本
  • 起止时间:
    2003 至 2005
  • 项目状态:
    已结题

项目摘要

1.Changes in Strongyloides venezuelensis larvae upon entry into the hostInfective larvae of S.venezuelensis has a matrix metalloprotease. We found that this activity disappeared right after the entry into the host, which was associated with the disappearance of skin penetration ability. In addition to the percutaneous infectivity and metalloprotease activity, drastic changes in locomotion occurred in larvae. In order to identify factors that caused these changes in larvae, we cultured infective larvae in serum-free culture medium at 37 degrees for 3 days. We clearly demonstrated that infective larvae transformed into connective tissue larvae as judged by all parameters we examined. Trans formation required both temperature and nutritional factors.2.Secreted adhesion molecules of adult wormsAdult worms of S.venezuelensis have a potent mucoal invasion capacity, which was confirmed by surgically implanted adult worms invading into chick small intestine. During tissue migration, larvae started expressing adhesion molecules, which are essentially important in mucosal invasion in the lungs.3.Effets of secreted antigens on host immune systemS.venezuelensis is usually expelled from the host by mucosal mast cells which are T cell-dependent. However, in IL-5 transgenic mice, hyperactivated eosinophils infiltrated into epithelial layer of small intestine and cleared mucosal adult worms. Studies on T cell induction in S. venezuelensis infected mice revealed that collaboration between IL-18-dependent mastocytosis before antigenic activation of T cells, and Th2 cell-dependent mastocytosis is important for prompt parasite expulsion.
1.委内瑞拉圆线虫幼虫进入宿主后的变化委内瑞拉圆线虫感染性幼虫具有基质金属蛋白酶。我们发现这种活性在进入宿主后立即消失,这与皮肤渗透能力的消失有关。除了经皮感染性和金属蛋白酶活性外,幼虫的运动也发生了剧烈变化。为了确定引起幼虫这些变化的因素,我们将感染性幼虫在无血清培养基中37度培养3天。我们清楚地证明,根据我们检查的所有参数判断,感染性幼虫转化为结缔组织幼虫。转化需要温度和营养因素的共同作用。 2.成虫分泌的粘附分子 委内瑞拉链球菌成虫具有强大的粘膜侵袭能力,通过手术植入成虫侵入雏鸡小肠证实了这一点。在组织迁移过程中,幼虫开始表达粘附分子,这对于肺部粘膜侵袭至关重要。3.分泌抗原对宿主免疫系统的影响委内瑞拉链球菌通常通过T细胞依赖性粘膜肥大细胞从宿主体内排出。然而,在IL-5转基因小鼠中,过度活化的嗜酸性粒细胞浸润到小肠上皮层并清除粘膜成虫。对委内瑞拉沙门氏菌感染小鼠中 T 细胞诱导的研究表明,T 细胞抗原激活前的 IL-18 依赖性肥大细胞作用和 Th2 细胞依赖性肥大细胞作用之间的协作对于迅速驱除寄生虫至关重要。

项目成果

期刊论文数量(36)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
家庭医学大全科:線虫によっておきる病気(寄生虫・原虫で起こる感染症)
家庭医学百科全书:线虫引起的疾病(寄生虫、原虫引起的传染病)
  • DOI:
  • 发表时间:
    2004
  • 期刊:
  • 影响因子:
    0
  • 作者:
    丸山治彦
  • 通讯作者:
    丸山治彦
Adult worms of the rodent intestinal nematode, Strongyloides venezuelensis, successfully invade chick intestinal mucosa.
啮齿动物肠道线虫委内瑞拉圆线虫成虫成功侵入雏鸡肠粘膜。
  • DOI:
  • 发表时间:
    2003
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Maruyama H;Aoki M;Okamura S;Yoshida A;Itagaki T;Ohta N
  • 通讯作者:
    Ohta N
ntraepithelial infiltration of eosinophils and their contribution to the elimination of adult intestinal nematode, Strongyloides venezuelensis in mice.
嗜酸性粒细胞上皮内浸润及其对消除小鼠成虫肠道线虫委内瑞拉类圆线虫的贡献。
  • DOI:
  • 发表时间:
    2004
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Mohamed El-Malky;Haruhiko Maruyama;Yoshiaki Hirabayashi;Shoichi Shimada;Ayako Yoshida;Teruaki Amano;Akira Tominaga;Kiyoshi Takatsu;Nobuo Ohta.
  • 通讯作者:
    Nobuo Ohta.
分子寄生虫学入門:寄生虫を作る(C.elegans寄生虫化計画)
分子寄生虫学简介:创建寄生虫(线虫寄生项目)
  • DOI:
  • 发表时间:
    2005
  • 期刊:
  • 影响因子:
    0
  • 作者:
    丸山治彦
  • 通讯作者:
    丸山治彦
よくみられる消化管線虫症の疑いから治療まで(特集:寄生虫とペット病-新たな認識と実地診療)
常见胃肠类圆线虫病从怀疑到治疗(专题:寄生虫与宠物疾病——新认识与实用治疗)
  • DOI:
  • 发表时间:
    2004
  • 期刊:
  • 影响因子:
    0
  • 作者:
    El-Malky;Lu;Kumagai;Yabu;Noureldin;Saudy;Maruyama;et al.;丸山治彦
  • 通讯作者:
    丸山治彦
{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ monograph.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ sciAawards.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ conferencePapers.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ patent.updateTime }}

MARUYAMA Haruhiko其他文献

Research concept: Seroepidemiology of strongyloidiasis to reveal an accurate distribution in Kenya
研究理念:类圆线虫病血清流行病学揭示肯尼亚的准确分布
  • DOI:
  • 发表时间:
    2019
  • 期刊:
  • 影响因子:
    0
  • 作者:
    HYUGA Ayako;MORIYASU Taeko;Samson Muuo NZOU;MARUYAMA Haruhiko;KANEKO Satoshi
  • 通讯作者:
    KANEKO Satoshi

MARUYAMA Haruhiko的其他文献

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

{{ truncateString('MARUYAMA Haruhiko', 18)}}的其他基金

Elucidation of pathophysiology of congenital factor XII deficiency in cat for the development of novel antithrombotic therapy
阐明猫先天性因子 XII 缺乏症的病理生理学,以开发新型抗血栓治疗
  • 批准号:
    18K06004
  • 财政年份:
    2018
  • 资助金额:
    $ 2.3万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Research on canine thrombotic disease with focus on ADAMTS13 and VWF
以 ADAMTS13 和 VWF 为重点的犬血栓性疾病研究
  • 批准号:
    25850213
  • 财政年份:
    2013
  • 资助金额:
    $ 2.3万
  • 项目类别:
    Grant-in-Aid for Young Scientists (B)
Isolation of longevity related genes of prasitic nematodes with east epression system
东表达系统分离寄生线虫长寿相关基因
  • 批准号:
    24659190
  • 财政年份:
    2012
  • 资助金额:
    $ 2.3万
  • 项目类别:
    Grant-in-Aid for Challenging Exploratory Research
Basic research on establishing of novel diagnosis and therapy using ADAMTS13 in dog with thrombosis.
使用 ADAMTS13 建立犬血栓形成新诊断和治疗的基础研究。
  • 批准号:
    23780327
  • 财政年份:
    2011
  • 资助金额:
    $ 2.3万
  • 项目类别:
    Grant-in-Aid for Young Scientists (B)
Studies on the infection mechanisms of Strongyloides venezelensis by analyzing genes expressed in infective larvae.
通过分析感染性幼虫表达的基因来研究威尼斯类圆线虫的感染机制。
  • 批准号:
    21590466
  • 财政年份:
    2009
  • 资助金额:
    $ 2.3万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Development of an oral vaccine against strongyloidiasis
开发针对类圆线虫病的口服疫苗
  • 批准号:
    11670247
  • 财政年份:
    1999
  • 资助金额:
    $ 2.3万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)

相似海外基金

Analysis of the function of ketone bodies in the intestinal mucosa of inflammatory bowel diesase
酮体在炎症性肠病肠黏膜中的功能分析
  • 批准号:
    23K07435
  • 财政年份:
    2023
  • 资助金额:
    $ 2.3万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Effects of sex-dependent susceptibility to CNS inflammatory demyelination on the intestinal mucosa
性别依赖性中枢神经系统炎症性脱髓鞘易感性对肠粘膜的影响
  • 批准号:
    10731325
  • 财政年份:
    2022
  • 资助金额:
    $ 2.3万
  • 项目类别:
Targeting the Intestinal Mucosa and Microbiome to Prevent Neonatal Late-onset Sepsis
针对肠粘膜和微生物组预防新生儿迟发性脓毒症
  • 批准号:
    10458103
  • 财政年份:
    2021
  • 资助金额:
    $ 2.3万
  • 项目类别:
Targeting the Intestinal Mucosa and Microbiome to Prevent Neonatal Late-onset Sepsis
针对肠粘膜和微生物组预防新生儿迟发性脓毒症
  • 批准号:
    10317586
  • 财政年份:
    2021
  • 资助金额:
    $ 2.3万
  • 项目类别:
Targeting the Intestinal Mucosa and Microbiome to Prevent Neonatal Late-onset Sepsis
针对肠粘膜和微生物组预防新生儿迟发性脓毒症
  • 批准号:
    10677884
  • 财政年份:
    2021
  • 资助金额:
    $ 2.3万
  • 项目类别:
Elucidation of the mechanisms of host physiological homeostasis by intestinal mucosa-associated microbiota
肠粘膜相关微生物群阐明宿主生理稳态机制
  • 批准号:
    20K16251
  • 财政年份:
    2020
  • 资助金额:
    $ 2.3万
  • 项目类别:
    Grant-in-Aid for Early-Career Scientists
Immune responses to commensal bacterial spores in the intestinal mucosa
对肠粘膜共生细菌孢子的免疫反应
  • 批准号:
    10170250
  • 财政年份:
    2020
  • 资助金额:
    $ 2.3万
  • 项目类别:
Immune responses to commensal bacterial spores in the intestinal mucosa
对肠粘膜共生细菌孢子的免疫反应
  • 批准号:
    10041895
  • 财政年份:
    2020
  • 资助金额:
    $ 2.3万
  • 项目类别:
Analysis of intestinal mucosa-associated microbiota involved in progression to non-alcoholic steatohepatitis
参与非酒精性脂肪性肝炎进展的肠粘膜相关微生物群分析
  • 批准号:
    19K07938
  • 财政年份:
    2019
  • 资助金额:
    $ 2.3万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Physiological and pathological analysis of intestinal mucosa lymphatic endothelial cells.
肠粘膜淋巴内皮细胞的生理病理分析。
  • 批准号:
    19K22665
  • 财政年份:
    2019
  • 资助金额:
    $ 2.3万
  • 项目类别:
    Grant-in-Aid for Challenging Research (Exploratory)
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了