A role of osteopontin in ulcerative colitis

骨桥蛋白在溃疡性结肠炎中的作用

基本信息

  • 批准号:
    15591446
  • 负责人:
  • 金额:
    $ 2.11万
  • 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 2004
  • 项目状态:
    已结题

项目摘要

Ulcerative colitis(UC) is a multifactorial disorder of unknown etiology. Few studies have applied genome-wide gene expression analysis in colon tissue samples of UC. We performed the analysis of gene expression in UC and noninflamed control specimens using high-density oligonucleotide array system (Affymetrix GeneChip^<【○!R】> System, Santa Clara, CA). In addition, using the antibody against the gene product that was expressed most remarkably in the colon tissue of UC, immunohistochemistry(IHC) study was performed in colon tissues of ulcerative colitis(UC), Crohn's disease(CD) and diverticulitis(Div) patients. Methods : To compare differences in the level of gene expression between UC and control samples, 10 colonic tissue samples (7 UC and 3 normal control samples) were subjected to high-density oligonucleotide array analysis. In addition, IHC staining study for the remarkable expressed gene product was performed in three groups : UC group, CD(Crohn's disease) group, Div(diverticulitis … More ) group. Results : 1)Twenty five genes had a 3.0〜23.4-fold higher mRNA expression in UC samples compared with normal samples. Among the 25 genes, only two genes varied by more than 10-fold and a gene with the strongest expression was osteopontin(OPN). 2)Regarding OPN expression by IHC in intestinal epithelial cells, no difference was noted among the three groups. However, in the submucosa of the UC group, the ratio of two types of large cells (oval and spindle shape) expressing OPN was 61.2±14.4% (mean±SD), which was a significantly higher ratio than the CD group (14.9±7.0%) (p<0.05) and the Div group (11.2±6.1%) (p<0.05). In addition, the ratio of the UC group in the subserosa (50.1±15.0% )(mean±SD) was significantly higher than the CD group (16.9±6.2%) and Div group (12.6±5.7%). Based on the serial section study, oval shape cells were stained for anti-CD 68,while spindle shape cells were stained for anti-vimentin. Conclusion : Our present study indicates the possibility that osteopontin plays an important role in one of the pathogenesis of UC via increased immune activity. Less
溃疡性结肠炎(UC)是一种病因不明的多因素疾病。很少有研究将全基因组基因表达分析应用于UC的结肠组织样本。我们使用高密度寡核苷酸阵列系统(Affymetrix GeneChip^&lt;[0!R]&gt;System,Santa Clara,CA)分析了UC和非炎症对照标本中的基因表达。此外,利用在UC结肠组织中表达最显著的基因产物的抗体,对溃疡性结肠炎(UC)、克罗恩病(CD)和憩室炎(Div)患者的结肠组织进行了免疫组织化学(IHC)研究。方法:采用高密度寡核苷酸芯片技术对10例结肠组织标本(7例UC和3例正常对照)的基因表达水平进行比较。此外,对UC组、CD(克罗恩病)组、DiV(憩室炎…)组的显著表达基因产物进行了免疫组织化学染色研究更多)组。结果:1)25个基因在UC组织中的表达水平是正常对照组的3.0~23.4倍。在25个基因中,只有两个基因的差异超过10倍,其中表达最强的基因是骨桥蛋白(OPN)。2)肠上皮细胞IHC表达OPN,三组间差异无统计学意义。在UC组粘膜下层,卵圆形和梭形两种大细胞表达OPN的比例为61.2±14.4%(平均值±SD),显著高于CD组(14.9±7.0%)和Div组(11.2±6.1%)(P&lt;0.05)。UC组浆膜下比例(50.1±15.0%)显著高于CD组(16.9±6.2%)和Div组(12.6±5.7%)。在连续切片的基础上,对卵圆形细胞进行抗CD68染色,对梭形细胞进行抗波形蛋白染色。结论:本研究提示骨桥蛋白可能通过增强免疫活性在UC发病机制中发挥重要作用。较少

项目成果

期刊论文数量(8)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Hideki Masuda: "Distinct Gene Expression of Osteopontin in Patients with Ulcerative Colitis"Journal of Surgical Research. 111.1. 85-90 (2003)
Hideki Masuda:“溃疡性结肠炎患者骨桥蛋白的独特基因表达”外科研究杂志。
  • DOI:
  • 发表时间:
  • 期刊:
  • 影响因子:
    0
  • 作者:
  • 通讯作者:
Distinct Gene Expression of Osteopontin in Patients with Ulcerative Colitis
溃疡性结肠炎患者骨桥蛋白的独特基因表达
  • DOI:
  • 发表时间:
    2003
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Hideki Masuda;Yasuo Takahashi;Satoshi Asai;Tadatoshi Takayama
  • 通讯作者:
    Tadatoshi Takayama
Osteopontin expression in ulcerative colitis is distinctly different From Crohn's disease and diverticulitis
溃疡性结肠炎中骨桥蛋白的表达与克罗恩病和憩室炎明显不同
  • DOI:
  • 发表时间:
    2005
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Iwaya T;Maesawa C;Kimura T;Ogasawara S;Ikeda K;Kimura Y;Noda Y;Ishida K;Sato N;Saito K;Masuda T.;Hideki Masuda et al.
  • 通讯作者:
    Hideki Masuda et al.
Osteopontin expression in ulcerative colitis is distinctly different from that in Crohn' s disease and diverticulitis.
溃疡性结肠炎中的骨桥蛋白表达与克罗恩病和憩室炎中的骨桥蛋白表达明显不同。
  • DOI:
  • 发表时间:
    2005
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Harada C;Harada T;Mitamura Y;Quah AH-M;Ohtsuka K;Kotake S;Ohno S;Wada K;Takeuchi S;Tanaka K;桑名正隆;Watanabe H;Yamakawa K.;Masuda H
  • 通讯作者:
    Masuda H
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MASUDA Hideki其他文献

MASUDA Hideki的其他文献

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{{ truncateString('MASUDA Hideki', 18)}}的其他基金

Organic thin-film solar cell based on localized surface plasmon resonance
基于局域表面等离子体共振的有机薄膜太阳能电池
  • 批准号:
    24655176
  • 财政年份:
    2012
  • 资助金额:
    $ 2.11万
  • 项目类别:
    Grant-in-Aid for Challenging Exploratory Research
Development of Health and Environment Checking Sensors Inspired from Biological Functions
受生物功能启发开发健康和环境检查传感器
  • 批准号:
    22350028
  • 财政年份:
    2010
  • 资助金额:
    $ 2.11万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Fabrication of anodic porous alumina with reduced hole interval and its application for the high-density magnetic recording media
缩小孔距阳极多孔氧化铝的制备及其在高密度磁记录介质中的应用
  • 批准号:
    21245048
  • 财政年份:
    2009
  • 资助金额:
    $ 2.11万
  • 项目类别:
    Grant-in-Aid for Scientific Research (A)
T cell function in ulcerative colitis, particularly relationship between osteopontin and ulcerative colitis
溃疡性结肠炎中的T细胞功能,特别是骨桥蛋白与溃疡性结肠炎之间的关系
  • 批准号:
    20591595
  • 财政年份:
    2008
  • 资助金额:
    $ 2.11万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Construction of Bio-inorganic Devices Having Chemical/Energy Conversion Functions
具有化学/能量转换功能的生物无机器件的构建
  • 批准号:
    19350083
  • 财政年份:
    2007
  • 资助金额:
    $ 2.11万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Preparation of Ordered Anodic Porous Alumina and Its Functional Applications
有序阳极多孔氧化铝的制备及其功能应用
  • 批准号:
    17205019
  • 财政年份:
    2005
  • 资助金额:
    $ 2.11万
  • 项目类别:
    Grant-in-Aid for Scientific Research (A)
Study on properties of long-range ordering of hole arrangement in anodic porous alumina
阳极多孔氧化铝孔排列长程有序特性研究
  • 批准号:
    14350456
  • 财政年份:
    2002
  • 资助金额:
    $ 2.11万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Gene expression of colonic mucosa in patients with ulcerative colitis using oligonucleotide array-based technology
使用基于寡核苷酸阵列的技术研究溃疡性结肠炎患者结肠粘膜的基因表达
  • 批准号:
    13671349
  • 财政年份:
    2001
  • 资助金额:
    $ 2.11万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Construction of Self-assembled Hybridized Materials Having Intelligent Functions
具有智能功能的自组装杂化材料的构建
  • 批准号:
    12304039
  • 财政年份:
    2000
  • 资助金额:
    $ 2.11万
  • 项目类别:
    Grant-in-Aid for Scientific Research (A)
Construction of in situ, time-resolved, and temperature-changeable spectrometry
原位、时间分辨、变温光谱测定的构建
  • 批准号:
    11554026
  • 财政年份:
    1999
  • 资助金额:
    $ 2.11万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)

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Tissue tropism of PD-1 therapy in ulcerative colitis and rheumatoid arthritis
PD-1治疗溃疡性结肠炎和类风湿性关节炎的组织向性
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    MR/Y009681/1
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    23K11871
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    2023
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Expression mechanism of Schlafen11 in ulcerative colitis and its usefulness as a biomarker
Schlafen11在溃疡性结肠炎中的表达机制及其作为生物标志物的用途
  • 批准号:
    23K15029
  • 财政年份:
    2023
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    Grant-in-Aid for Early-Career Scientists
Pathophysiology of Ulcerative Colitis and Primary Sclerosing Cholangitis by Immune Commonality
免疫共性的溃疡性结肠炎和原发性硬化性胆管炎的病理生理学
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    23K15032
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    2023
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Dysregulation of Epithelial Metabolism and Regeneration by Sulfite Exposure in Pediatric Ulcerative Colitis
小儿溃疡性结肠炎亚硫酸盐暴露导致上皮代谢和再生失调
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    10722914
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Development of Patient-Tailored Adaptive Treatment Strategies for Acute Severe Ulcerative Colitis
制定针对急性重症溃疡性结肠炎的患者定制适应性治疗策略
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Identifying Neutrophil Specific Mechanisms for Resistance to Biologics in Ulcerative Colitis
确定中性粒细胞对溃疡性结肠炎生物制剂耐药的特异性机制
  • 批准号:
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溃疡性结肠炎的免疫调节治疗
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    10697464
  • 财政年份:
    2023
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    $ 2.11万
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Clarification of the mechanism of the treatment-resistance in ulcerative colitis and establishment of the treatment strategy for it
溃疡性结肠炎耐药机制的阐明及治疗策略的制定
  • 批准号:
    23K07377
  • 财政年份:
    2023
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Hyperbaric Oxygen Therapy for Ulcerative Colitis Patients Hospitalized for Moderate to Severe Flares: A Phase 3 Multi-Center, Randomized, Double-Blind, Sham-Controlled Trial
高压氧治疗因中度至重度发作而住院的溃疡性结肠炎患者:一项 3 期多中心、随机、双盲、假对照试验
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    10561414
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    2023
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    $ 2.11万
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