Immunohistologial study on the expression of developmental intestinal epithelial antigens in embryogenesis and oncogenesis.

胚胎发生和肿瘤发生中发育肠上皮抗原表达的免疫组织学研究。

基本信息

  • 批准号:
    14570499
  • 负责人:
  • 金额:
    $ 2.18万
  • 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
  • 起止时间:
    2002 至 2004
  • 项目状态:
    已结题

项目摘要

1.Monoclonal antibodies that can be used for immunohistostaining of the formalin-fixed tissues were established to study the expression of the developmental antigens in rat embryonal and cancerous intestinal epithelia. Using the synthetic oligopeptides, mouse monoclonal antibodies against sucrase-isomaltase, MUC2 tandem and non-tandem repeat antigens, Cdx1, Cdx2, and Musashi1 were established.2.Expression of developmental intestinal epithelial antigens was studied immunohistochemically using the newly established monoclonal antibodies and the fixed tissues of embryonal rat intestines. Cdx2 was found to be expressed in the nuclei of endodermal cells at day 11 pc, but Cdx1 was first detected at day 15 pc. As the intestinal villi developed, Cdx1 and Cdx2, respectively, tended to localize in the intervillous endoderms and the villous epithelia. Although both of MUC2 and sucrase-isomaltase were synthesized and expressed before birth, the former expression preceded three days of the latter expression that was first detected at day 19 pc. The expression of Cdxs was not simply correlated with those of MUC2 and sucrase-isomlatase.3.Expression of apomucins, the blood group-related carbohydrate antigens and Cdx2 in the AOM-induced rat intestinal tumors was studied. Their expressions were generally suppressed in the tumors, though MUC5AC and H-antigen were observed to be expressed in the tissues not expressing them normally. Quantitative, but not qualitative, differences in the expression existed between the adenomas and the cancers. Although B-antigen expressed in the proximal colon might be carried by MUC5AC, there was no apparent association between the expressions of apomucins, the carbohydrate antigens and Cdx2. Expression of Cdx2 was almost completely suppressed in the AOM tumors.
1.建立了可用于福尔马林固定组织的免疫组织的单克抗体,以研究大鼠胚胎和癌性肠上皮中的发育抗原的表达。使用合成寡肽,对抗硫酶 - 异构酶,MUC2串联和非串联重复抗原,CDX1,CDX2和Musashi1的小鼠单克隆抗体进行表达。肠。发现CDX2在第11天PC中在内皮细胞的核中表达,但在第15天首先检测到CDX1。随着肠绒毛的发展,CDX1和CDX2分别倾向于本地化的内胚层和绒毛上皮。尽管MUC2和Sucrase-异构酶均在出生前合成并表达,但前者的表达在后一种表达的三天之前首次在第19天PC上检测到。 CDX的表达不仅与MUC2和Sucrase-Isomlatase的表达相关。3。Apomucins在AOM诱导的大鼠肠道肿瘤中的表达,与血型相关的碳水化合物抗原和CDX2相关。尽管观察到在不正常表达它们的组织中表达的MUC5AC和H-抗原,但它们的表达通常在肿瘤中受到抑制。腺瘤和癌症之间存在定量但不是定性的差异。尽管在近端结肠中表达的B抗原可能是MUC5AC携带的,但阿哌辛蛋白,碳水化合物抗原和CDX2的表达之间没有明显的关联。在AOM肿瘤中,CDX2的表达几乎被完全抑制。

项目成果

期刊论文数量(18)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
A Colonic expression of MUC2, MUC5AC, and TFF1 in inflammatory bowel disease in children
儿童炎症性肠病中 MUC2、MUC5AC 和 TFF1 的结肠表达
Kaneko Y, Yanagihara K, Hirata Y, Mukae H, Tomono K, Okada Y, Kadota J, Kohno S: "Overproduction of MUC5AC core protein in patients with diffuse panbronchiolitis"Respiration. 70. 475-478 (2003)
Kaneko Y、Yanagihara K、Hirata Y、Mukae H、Tomono K、Okada Y、Kadota J、Kohno S:“弥漫性全细支气管炎患者中 MUC5AC 核心蛋白的过量产生”呼吸。
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
  • 作者:
  • 通讯作者:
Shaoul R, Marcon P.Okada Y, Cutz E, Marcon MA: "Colonic expression of MUC2,MUC5AC and TFF1 in inflammatory bowel disease in children"J Pediat Gastroenterol Nutr. (印刷中). (2004)
Shaoul R、Marcon P.Okada Y、Cutz E、Marcon MA:“儿童炎症性肠病中 MUC2、MUC5AC 和 TFF1 的结肠表达”J Pediat Gastroenterol Nutr(出版中)。
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
  • 作者:
  • 通讯作者:
Mapping of SOMU1 and M1 epitopes on the apomucin encoded by the 5' end of the MUC5AC gene
MUC5AC 基因 5 端编码的 apomucin 上 SOMU1 和 M1 表位的定位
  • DOI:
  • 发表时间:
    2004
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Nollet S;Escande F;Buisine MP;Forgue-Lafitte ME;Kirkham P;Okada Y;Bara J
  • 通讯作者:
    Bara J
Nollet S.Escande F, Buisine MP, Forgue LME, Kirkham P, Okada Y, Bara J: "Mapping of SOMU1 and M1 epitopes on the apomucin encoded by the 5' end of the MUC5AC gene"Hybridoma and Hybridomics. (印刷中). (2004)
Nollet S.Escande F、Buisine MP、Forgue LME、Kirkham P、Okada Y、Bara J:“MUC5AC 基因 5 端编码的 apomucin 上 SOMU1 和 M1 表位的映射”杂交瘤和杂交组学(出版中)。 (2004)
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    0
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OKADA Yoshio其他文献

OKADA Yoshio的其他文献

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{{ truncateString('OKADA Yoshio', 18)}}的其他基金

Curriculum Development based on the children's learning ability
基于孩子学习能力的课程开发
  • 批准号:
    11680270
  • 财政年份:
    1999
  • 资助金额:
    $ 2.18万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Design and synthesis of μ-selective opioidomimetic peptides
μ选择性阿片样肽的设计与合成
  • 批准号:
    11694326
  • 财政年份:
    1999
  • 资助金额:
    $ 2.18万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Infectious disease, and hepatic and gastrointestinal disease in Japan and China
日本和中国的传染病、肝脏和胃肠道疾病
  • 批准号:
    07045049
  • 财政年份:
    1995
  • 资助金额:
    $ 2.18万
  • 项目类别:
    Grant-in-Aid for international Scientific Research
Gene cloning of a novel apomucin expressed in human gastric surface epithelia and parietal cells
人胃表面上皮和壁细胞表达的新型阿普粘蛋白的基因克隆
  • 批准号:
    07670608
  • 财政年份:
    1995
  • 资助金额:
    $ 2.18万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Gastrointestinal and hematologic diseases in Japan and China
日本和中国的胃肠道和血液疾病
  • 批准号:
    06045020
  • 财政年份:
    1994
  • 资助金额:
    $ 2.18万
  • 项目类别:
    Grant-in-Aid for international Scientific Research
Studies on the difference in the circumstances and the diseases between Japanese and Chinese
日本人和中国人的环境和疾病差异研究
  • 批准号:
    05045047
  • 财政年份:
    1993
  • 资助金额:
    $ 2.18万
  • 项目类别:
    Grant-in-Aid for international Scientific Research
Experimental Sutdies for Application of the Heterogeneous Lung as Oxygenator
应用异质肺作为氧合器的实验研究
  • 批准号:
    01440056
  • 财政年份:
    1989
  • 资助金额:
    $ 2.18万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (A)
Basic Researches on Cell Fusion and Their Application to Cell Technology
细胞融合基础研究及其在细胞技术中的应用
  • 批准号:
    01102028
  • 财政年份:
    1989
  • 资助金额:
    $ 2.18万
  • 项目类别:
    Grant-in-Aid for Co-operative Research (A).
FUNDAMENTAL AND CLINICAL RESEARCH ON THE RELATIONSHIP BETWEEN PULMONARY LYMPHATIC SYSTEMS AND THE PATHOGENESIS OF VARIOUS LUNG DISEASES
肺淋巴系统与多种肺部疾病发病关系的基础和临床研究
  • 批准号:
    60440062
  • 财政年份:
    1985
  • 资助金额:
    $ 2.18万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (A)

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Molecular Studies on MUC4 Mucin Gene
MUC4粘蛋白基因的分子研究
  • 批准号:
    7909936
  • 财政年份:
    2009
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  • 项目类别:
Smoking and pancreatic cancer
吸烟与胰腺癌
  • 批准号:
    8010192
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Smoking and pancreatic cancer
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  • 批准号:
    8009975
  • 财政年份:
    2008
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  • 项目类别:
Molecular Studies on MUC4 Mucin Gene
MUC4粘蛋白基因的分子研究
  • 批准号:
    7877014
  • 财政年份:
    2008
  • 资助金额:
    $ 2.18万
  • 项目类别:
Smoking and pancreatic cancer
吸烟与胰腺癌
  • 批准号:
    8205008
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