Microarray and proteomics analysis on odontogenesis-related-genes in prenatal mouse dental papillae

产前小鼠牙乳头成牙相关基因的微阵列和蛋白质组学分析

基本信息

  • 批准号:
    17591926
  • 负责人:
  • 金额:
    $ 2.21万
  • 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:
    2005
  • 资助国家:
    日本
  • 起止时间:
    2005 至 2007
  • 项目状态:
    已结题

项目摘要

Important factors for involved in odontogenesis in mouse dental papillae have been reported to disappear between the pre- and post-natal stages of development. Therefore, we hypothesized that the genes involved in odontogenesis in dental papillae might be down-regulated after birth. Our goal was to identify those which genes were down-regulated genes by microarray analysis. Dental papillae were dissected isolated from embryonic of 16-day and 18-day (E16, E18), and post-natal 3- and 10-day-old (P3, P10) murine mice first mandibular molar germs. The highest number of down-regulated genes (2924) was found at E18 and P3 Down-regulation of Adamts4 and Aldhala2 was found at both E16 and E18, and expression of Plxncl showed a reduction at E18 and P3. Investigation of expression of Adamts4, Aldhla2 and Plxncl was investigated by quantitative RT-PCR which showed revealed a reduction of in their expression after birth (Adamts4; 1/3, Aldhla2; 1/13, Plxncl; 1/3). These results suggest that three of the genes selected identified by the microarray analysis - Adamts4, Aldhla2, and Plxncl - are involved in odontogenesisin dental papillae.
据报道,在发育前和产后阶段之间,涉及小鼠牙皮乳头的牙肠发生的重要因素。因此,我们假设牙齿乳头状的牙肠发生的基因可能会在出生后下调。我们的目标是通过微阵列分析鉴定基因下调基因的基因。从16天和18天(E16,E18)的胚胎中分离出牙皮乳头,以及3天和10天大的幼虫(P3,P10)鼠小鼠首次下颌摩尔细菌。在E18时发现了最多的下调基因(2924),并且在E16和E18上都发现了ADAMTS4和ALDHALA2的P3下调,PLXNCL的表达在E18和P3时显示出降低。通过定量RT-PCR研究了ADAMTS4,Aldhla2和PLXNCL的表达的研究,该定量RT-PCR显示出出生后其表达的降低(Adamts4; 1/3; 1/3,Aldhla2; 1/13; 1/13,plxncl; 1/3)。这些结果表明,通过微阵列分析鉴定的三个基因 - ADAMTS4,Aldhla2和PLXNCL - 参与牙乳状核酸酯的牙胎。

项目成果

期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
The epithelial-mesenchymal interaction for tooth morphogenes is with special reference to the arrest of normal tooth development in the diastema budding
牙齿形态发生的上皮-间质相互作用特别涉及纵裂出芽时正常牙齿发育的停滞
Gene Chipマイクロアレイによるマウス臼歯の歯乳頭、歯髄の遺伝子発現の比較
使用基因芯片微阵列比较小鼠磨牙牙乳头和牙髓中的基因表达
  • DOI:
  • 发表时间:
    2005
  • 期刊:
  • 影响因子:
    0
  • 作者:
    佐々木 穂高;村松 敬;太田 一正;君塚 隆太;橋本 貞充;下野 正基
  • 通讯作者:
    下野 正基
Immunohistochemical localization for manganese and copper, zinc superoxide dismutase in secretory ameloblasts of rat incisor
大鼠门牙分泌性成釉细胞中锰、铜、锌超氧化物歧化酶的免疫组织化学定位
Ca^<2+> transporting/signaling mechanisms mediated by sodium/calcium exchangers in rat ameloblasts
大鼠成釉细胞中钠/钙交换剂介导的 Ca^2 转运/信号传导机制
  • DOI:
  • 发表时间:
    2007
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Okumura R;Suzuki K;Muramatsu T;Nakagawa K;Shimono M;Schnetkamp P PM;Shibukawa Y.
  • 通讯作者:
    Shibukawa Y.
歯性間葉組織がもつ歯の潜在的形成能について
关于牙源性间充质组织潜在的牙齿形成
  • DOI:
  • 发表时间:
    2006
  • 期刊:
  • 影响因子:
    0
  • 作者:
    山本 仁;脇坂 聡;土門 卓文;斎藤 正寛;今井 元;Herve Lesot;小澤 幸重
  • 通讯作者:
    小澤 幸重
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MURAMATSU Takashi其他文献

<i>In vitro</i> remineralization of enamel with a solution containing casein and fluoride
使用含有酪蛋白和氟化物的溶液<i>体外</i>牙釉质再矿化
  • DOI:
    10.4012/dmj.2020-383
  • 发表时间:
    2021
  • 期刊:
  • 影响因子:
    2.5
  • 作者:
    NAKAMURA Keiki;HAMBA Hidenori;MIYAYOSHI Yoshihito;ISHIZUKA Hisako;MURAMATSU Takashi
  • 通讯作者:
    MURAMATSU Takashi
Remineralization Potential of a Calcium - Fluoroaluminosilicate Glass-based Desensitizer on Artificial Human Enamel Subsurface Lesions
钙-氟铝硅酸盐玻璃基脱敏剂对人造人牙釉质表面下病变的再矿化潜力

MURAMATSU Takashi的其他文献

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{{ truncateString('MURAMATSU Takashi', 18)}}的其他基金

Research on the construction of teaching materials of digital picture story show for international understanding and international cooperation
促进国际理解与国际合作的数字绘本故事秀教材建设研究
  • 批准号:
    23531239
  • 财政年份:
    2011
  • 资助金额:
    $ 2.21万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Are odontogenesis-related genes detected with microarray really involved in odontogenesis?
微阵列检测到的牙发育相关基因真的参与牙发育吗?
  • 批准号:
    20592151
  • 财政年份:
    2008
  • 资助金额:
    $ 2.21万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Composition and mode of action of the midkine receptor
中期因子受体的组成和作用方式
  • 批准号:
    19590291
  • 财政年份:
    2007
  • 资助金额:
    $ 2.21万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Development of therapy for malignant tumors and inflammatory diseases employing midkine as a molecular target
以中期因子为分子靶标的恶性肿瘤和炎症性疾病治疗方法的开发
  • 批准号:
    15390103
  • 财政年份:
    2003
  • 资助金额:
    $ 2.21万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Recognition of sulfated hexosamine upon construction of the nervous system
神经系统构建过程中硫酸化己糖胺的识别
  • 批准号:
    14082202
  • 财政年份:
    2002
  • 资助金额:
    $ 2.21万
  • 项目类别:
    Grant-in-Aid for Scientific Research on Priority Areas
Biological significance of N-acetylglucosamine 6-sulfation
N-乙酰氨基葡萄糖6-硫酸化的生物学意义
  • 批准号:
    12480187
  • 财政年份:
    2000
  • 资助金额:
    $ 2.21万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Application of midkine to diagnosis and treatment of tumors and growth of blood stem cells.
中期因子在肿瘤诊治及造血干细胞生长中的应用。
  • 批准号:
    09557016
  • 财政年份:
    1997
  • 资助金额:
    $ 2.21万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Growth factor midkine : Biological significance, action mechanism, tissue repairing activity and relationship with diseases.
生长因子中期因子:生物学意义、作用机制、组织修复活性以及与疾病的关系。
  • 批准号:
    08457035
  • 财政年份:
    1996
  • 资助金额:
    $ 2.21万
  • 项目类别:
    Grant-in-Aid for Scientific Research (B)
Receptor structure and inhibition of midkine, a growth factor controled by retinoic acid
视黄酸控制的生长因子中期因子的受体结构和抑制
  • 批准号:
    06454645
  • 财政年份:
    1994
  • 资助金额:
    $ 2.21万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (B)
Studies on a new growth factor under the control of retinoic acid, midkine (MK)
视黄酸调控的新型生长因子中期因子(MK)的研究
  • 批准号:
    04454594
  • 财政年份:
    1992
  • 资助金额:
    $ 2.21万
  • 项目类别:
    Grant-in-Aid for General Scientific Research (B)

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Identification of novel calcification-inducing factors for anti-tumor therapy, and their role in tooth germ differentiation.
抗肿瘤治疗的新型钙化诱导因子的鉴定及其在牙胚分化中的作用。
  • 批准号:
    23H03109
  • 财政年份:
    2023
  • 资助金额:
    $ 2.21万
  • 项目类别:
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Genomic and functional investigations of the transcriptional regulatory network of tooth enamel development
牙釉质发育转录调控网络的基因组和功能研究
  • 批准号:
    10720303
  • 财政年份:
    2023
  • 资助金额:
    $ 2.21万
  • 项目类别:
The Role of CD4+ Memory T cell Subtypes in Periodontal Disease Recurrence
CD4 记忆 T 细胞亚型在牙周病复发中的作用
  • 批准号:
    10642981
  • 财政年份:
    2023
  • 资助金额:
    $ 2.21万
  • 项目类别:
Nonclassical β-catenin signaling in odontogenesis
牙发生中的非经典β-连环蛋白信号传导
  • 批准号:
    10714280
  • 财政年份:
    2023
  • 资助金额:
    $ 2.21万
  • 项目类别:
A Therapeutic Role for Apolipoprotein-E in the Germ Theory of Alzheimer's Dementia
载脂蛋白-E 在阿尔茨海默氏痴呆病菌理论中的治疗作用
  • 批准号:
    10601779
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    2023
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    $ 2.21万
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