Regulation of Genes in Mouse Temporomandibular Joint

小鼠颞下颌关节基因调控

• 批准号: 7989776
• 负责人: PATRICIA PURCELL
• 金额: $ 13.5万
• 依托单位: BOSTON CHILDREN'S HOSPITAL
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-09-22 至 2011-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7989776
• 关键词: Affect; Biological Markers; Biology; Cephalic; Complex; Development; Evaluation; Family; Gene Expression Profiling; Gene Expression Regulation; Genes; Genetic; Goals; Health; Joints; Knee; Knowledge; Lasers; Limb structure; Maintenance; Mammals; Mandibular Condyle; Mediator of activation protein; Messenger RNA; Microscopy; Molecular; Molecular Genetics; Morphogenesis; Mus; Mutant Strains Mice; Oligonucleotides; Phenotype; Population; Process; Regulator Genes; Research; Research Personnel; Role; Sampling; Signal Transduction; Staging; Structure; Synovial Fluid; Temporal bone structure; Temporomandibular Joint; Temporomandibular Joint Disorders; Testing; Vertebrates; base; bone; capsule; chordin; density; design; in vivo; member; mouse model; novel therapeutic intervention; programs; scleraxis

Description (provided by applicant): The overall goal of my research is to elucidate the molecular mechanisms involved in the formation and maintenance of the temporomandibular joint (TMJ), a highly specialized synovial joint found only in mammals. Presently, there is a lack of information about the molecular signals participating in these processes. Previous studies in the limb have indicated that regulatory genes controlling the formation of synovial joints are highly conserved among vertebrates. Studies included in this proposal are based on the hypothesis that "the basic genetic mechanisms regulating synovial joint development are conserved, but TMJ specific genes are also involved during TMJ formation". I will pursue three specific aims: in Aim 1 I will detail the stages of TMJ development in the mouse and investigate the presence of a well-defined group of regulatory genes known to control synovial joint formation in the limb; in Aim 2, I will identify specific regulators and biological markers of TMJ morphogenesis using a high density microarray approach; and in Aim 3, I will test the relevance of these candidate regulatory genes as mediators of TMJ morphogenesis using in vivo approaches. Collectively, these studies aim to close the current knowledge gap on the biology of the TMJ, a fundamental step toward designing novel therapeutic approaches for temporomandibular joint disorders, a significant health problem affecting approximately 12% of the U.S. population.

描述(申请人提供)：我研究的总体目标是阐明TMJ形成和维持的分子机制，TMJ是一种高度专门化的滑膜关节，仅在哺乳动物中发现。目前，关于参与这些过程的分子信号缺乏信息。以前对肢体的研究表明，控制滑膜关节形成的调控基因在脊椎动物中高度保守。这项建议中包含的研究是基于这样的假设：“调节滑膜关节发育的基本遗传机制是保守的，但TMJ特异性基因也参与了TMJ的形成”。我将追求三个具体目标：在目标1中，我将详细描述小鼠TMJ发育的各个阶段，并调查是否存在一组定义明确的调控基因，以控制肢体滑膜关节的形成；在目标2中，我将使用高密度微阵列方法确定TMJ形态发生的特定调控因子和生物标志物；在目标3中，我将使用体内方法测试这些候选调控基因作为TMJ形态发生介体的相关性。总而言之，这些研究旨在弥合目前对TMJ生物学的了解差距，这是朝着设计新的治疗方法治疗TMJ迈出的基本一步，TMJ是影响大约12%美国人口的重大健康问题。