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MMP-20 AND MMP-20 DOMAIN FUNCTION IN FORMING ENAMEL

MMP-20 AND MMP-20 DOMAIN FUNCTION IN FORMING ENAMEL
MMP-20 和 MMP-20 结构域在牙釉质形成中的功能
批准号:
6621467
负责人:
JOHN D BARTLETT
金额:
$38.58万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-01-01 至 2006-12-31

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中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The goal of this application is to characterize the role that the matrix metalloproteinase enamelysin (MMP-20) plays during dental enamel and tooth development. The enamel proteins (amelogenin, ameloblastin, enamelin) are cleaved soon after they are secreted into the enamel matrix. Enamelysin is expressed simultaneously with the enamel proteins and recombinant enamelysin will cleave recombinant amelogenin at virtually all of the precise sites previously observed in vivo. Thus, enamelysin is an important amelogenin processing enzyme. As for all MMPs, enamelysin contains a propeptide that must be cleaved if the enzyme is to become active. Enamelysin also has a hemopexin domain that is not functionally well defined. An enamelysin knockout (-/-) mouse was engineered to characterize the contribution of enamelysin to tooth and enamel development (Aim 1). The enamelysin -/-mouse is the only MMP -/- mouse with a profound phenotype that survives to breed. Thus, we can define the limits of the enamelysin promoter (Aim 2) so that it may be used to express an enamelysin transgene in the -/- background and revert the -/- phenotype back to normal. Furthermore, because the -/- mouse has a profound phenotype and can breed, we are in possession of the only MMP -/- mouse that can be utilized to characterize the mechanistic function of the MMP propeptide and/or hemopexin domain. So, we propose to introduce two enamelysin promoter transgenes into the -/-background. The first transgene will allow enamelysin to be secreted as an active enzyme (propeptide removed intracellularly) so that we may characterize the role of the enamelysin propeptide in tooth development (Aim 3). The second transgene will encode enamelysin without its' hemopexin domain so that the contribution of the hemopexin domain in tooth development may be characterized (Aim 4). The long-term goals of this project are to contribute to the understanding of enamel formation so that eventually synthetic enamel can be engineered for the repair of damaged (dental caries) or diseased (amelogenesis imperfecta) dental enamel. This application builds on results from a highly productive R29 grant (DE12098).
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Enamelysin Processing Mechanisms in Amelogenesis
  • 批准号:
    10316206
  • 项目类别:
  • 资助金额:
    $53.62万
  • 财政年份:
    2019
  • 负责人:
    JOHN D BARTLETT
  • 依托单位:
Enamelysin Processing Mechanisms in Amelogenesis
  • 批准号:
    10540711
  • 项目类别:
  • 资助金额:
    $54.16万
  • 财政年份:
    2019
  • 负责人:
    JOHN D BARTLETT
  • 依托单位:
THE ROLE OF STRESS AND PH IN FLUOROSIS
  • 批准号:
    9233520
  • 项目类别:
  • 资助金额:
    $26.09万
  • 财政年份:
    2016
  • 负责人:
    JOHN D BARTLETT
  • 依托单位:
Enamelysin processing mechanisms in amelogenesis
  • 批准号:
    9225454
  • 项目类别:
  • 资助金额:
    $2.52万
  • 财政年份:
    2016
  • 负责人:
    JOHN D BARTLETT
  • 依托单位:
国内基金
海外基金
重组Amelogenin多肽TRAP调节早期牙釉质龋仿生再矿化行为及机制研究
  • 批准号:
    U2004108
  • 项目类别:
    联合基金项目
  • 资助金额:
    50万元
  • 批准年份:
    2020
  • 负责人:
    楚金普
  • 依托单位:
重组Amelogenin和EMPs诱导骨髓基质细胞成骨分化及其调控机制的比较研究
  • 批准号:
    81070838
  • 项目类别:
    面上项目
  • 资助金额:
    35.0万元
  • 批准年份:
    2010
  • 负责人:
    束蓉
  • 依托单位:
amelogenin 基因修饰骨髓基质细胞促进牙周再生的实验研究
  • 批准号:
    30672315
  • 项目类别:
    面上项目
  • 资助金额:
    28.0万元
  • 批准年份:
    2006
  • 负责人:
    束蓉
  • 依托单位: