Modeling Dentin by G Protein Coupled Receptor Signaling

通过 G 蛋白偶联受体信号转导模拟牙本质

• 批准号: 8328604
• 负责人: Orapin V Horst
• 金额: $ 13.22万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-09-05 至 2016-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8328604
• 关键词: Address; Affect; Annual Reports; Applications Grants; Award; BMP4; Bone Matrix; California; Cell Communication; Cell Density; Cell Therapy; Cell physiology; Cells; Cellular biology; Centers for Disease Control and Prevention (U.S.); Clinical; Collagen Type I; Complex; Coupled; Cyclic AMP; Cytokeratin-14 Staining Method; Data; Dental; Dental Pulp; Dental caries; Dental crowns; Dentin; Dentin Formation; Dentists; Development; Development Plans; Developmental Biology; Discipline; Doctor of Philosophy; Drug Design; Educational workshop; Engineering; Environment; Environmental Risk Factor; Epithelial; Epithelial Cells; Epithelium; Event; FGF9 gene; Faculty; Failure; Fostering; Foundations; Funding; Future; G Protein-Coupled Receptor Signaling; G-Protein-Coupled Receptors; GTP-Binding Proteins; Goals; Growth Factor; Healed; Healthcare; Histocompatibility Testing; Hour; In Situ; Interdisciplinary Study; International; Journals; K-Series Research Career Programs; Knowledge; Lead; Learning; Ligands; Mediating; Medicine; Mentors; Mentorship; Mesenchymal; Mesenchymal Differentiation; Mesenchymal Stem Cells; Mesenchyme; Modeling; Molecular Biology; Morphology; Mus; National Institute of Dental and Craniofacial Research; Natural regeneration; Odontoblasts; Oral health; Phase; Physiological; Plant Roots; Production; Proteins; Pulp Chambers; Recurrence; Reporting; Research; Research Activity; Research Personnel; Research Training; Resources; Role; San Francisco; Schools; Scientist; Signal Pathway; Signal Transduction; Signaling Molecule; Specificity; Stem Cell Research; Stem cells; Testing; Tissue Engineering; Tissues; Tooth Cell; Tooth structure; Training; Training Support; Transgenic Mice; Tubular formation; Universities; Work; bone; career development; cell type; cost; cost effectiveness; dental genetics; experience; healing; improved; insight; keratin 5; malformation; material fatigue; member; mouse model; novel strategies; osteoblast differentiation; precursor cell; progenitor; programs; promoter; receptor; receptor function; repaired; research and development; restorative material; skills; transcription factor

DESCRIPTION (provided by applicant): This proposed application for a K08 Mentored Clinical Scientist Research Career Development Award is being submitted by Dr. Orapin Horst, a dentist-scientist at the University of California, San Francisco. This award will provide the support and training necessary for Dr. Horst to receive the mentoring to develop into an independent investigator, whereupon she will pursue her long-term goal of creating cell-based therapies and tissue engineering approaches to regenerate the dentin-pulp complex in a manner recapitulating normal development. She will have access to the many opportunities of UCSF to help her accomplish the following goals related to her career development: 1) to learn the disciplines of developmental biology and G protein coupled receptor (GPCR) signaling; 2) to experience interdisciplinary research with mentors experienced in basic to clinical translational work; 3) to build academic skills to become an outstanding research mentor and faculty member; 4) to develop skills in grantsmanship and obtaining funding; and 5) to collect pilot data for a future R01 application. To continue her progress towards these goals, Dr. Horst proposes a research plan that will elucidate signaling events between dental epithelial and mesenchymal progenitor cells to induce odontoblast differentiation and control the formation of the dentin-pulp complex. She will study these signaling events through the function of GPCRs, which have the potential to elicit or modify essentially any signaling pathway. Related findings have been reported in other cell and tissue types, in particular bone, but very little is known about GPCR function in teeth. The central hypothesis that will be tested in this K08 is that GPCR-modulated signaling molecules regulate odontoblast differentiation and dentin matrix formation. This hypothesis is addressed by the following specific aims: 1) To determine how Gs-coupled GPCR signals in dental mesenchymal cells including odontoblasts and preodontoblasts control dentin formation, and 2) To determine how Gs-coupled GPCR signals from dental epithelial cells modulate odontoblast differentiation. These aims will be pursued using a newly developed transgenic mouse model of G-protein signaling in mineralized tissue formation. Transgenic mice with increased Gs-coupled GPCR signals in odontoblasts and preodontoblasts driven by the type I collagen promoter will be used in Specific Aim 1, while mice with increased Gs-coupled GPCR signals in dental epithelial cells driven by the keratin 5 promoter will be used in Specific Aim 2. These studies will identify new interactions between GPCR signaling pathways and other mechanisms regulating odontoblast development and dentin matrix formation. Ultimately, these data will lay a foundation for an interdisciplinary research program and a R01 grant application to engineer a physiologic complex of tubular dentin supporting odontoblasts and pulp to heal carious teeth. The knowledge from this work will also improve our conceptual understanding of genetic dental malformations and environmental factors required for proper cell-matrix interactions to support normal development of dentin and other mineralized tissues. The proposed career development and research activities will take place in highly supportive, research- intensive environments. Two international experts in the developmental biology of teeth, Pamela DenBesten DDS, MS (primary mentor) and Ophir Klein MD, PhD (co-mentor), will supervise Dr. Horst's research focus on epithelial-mesenchymal interactions and formation of mineralized tissues. Two international experts in GPCR signaling, Bruce Conklin MD (co-mentor, GPCR signaling in stem cells) and Robert Nissenson PhD (co- mentor, GPCR signaling in bone), will supervise work with the transgenic mouse models, and relate their vast experience with other stem cell types and mineralized tissues, to understand the role of GPCR signaling in dental stem cells and the formation of the dentin-pulp complex. The mentors are all members of the new Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research of UCSF, which will serve as a central resource for training opportunities (workshops, seminars, journal clubs, and retreats) in combining expertise in developmental, molecular, and cellular biology with medically relevant foci such as that proposed in this project. The proposed research is part of a coordinated career development plan to prepare the candidate to be an outstanding, independent dentist-scientist through research, coursework, and tutorials. The interdisciplinary mentorship team will mentor the career development activities together, and facilitate Dr. Horst's natural progression from current research experiences to the mentored clinical scientist development phase and then to independence.

描述（由申请人提供）：本K 08指导临床科学家研究职业发展奖的拟议申请由加州大学旧金山弗朗西斯科的牙科科学家Orapin Horst博士提交。该奖项将为Horst博士提供必要的支持和培训，使其能够接受指导，发展成为一名独立的研究者，因此她将追求她的长期目标，即创建基于细胞的疗法和组织工程方法，以重现正常发育的方式再生牙本质牙髓复合体。她将有机会获得UCSF的许多机会，以帮助她实现与她的职业发展相关的以下目标：1）学习发育生物学和G蛋白偶联受体（GPCR）信号传导的学科; 2）与具有基础临床翻译工作经验的导师一起体验跨学科研究; 3）建立学术技能，成为优秀的研究导师和教师; 4）发展赠款和获得资金的技能; 5）为未来的R 01应用收集试验数据。为了继续实现这些目标，Horst博士提出了一项研究计划，该计划将阐明牙齿上皮细胞和间充质祖细胞之间的信号传导事件，以诱导成牙本质细胞分化并控制牙本质牙髓复合体的形成。她将通过GPCR的功能来研究这些信号事件，GPCR有可能引发或修改基本上任何信号通路。在其他细胞和组织类型，特别是骨骼中也有相关的发现，但对牙齿中GPCR的功能知之甚少。在K 08中将要检验的中心假设是GPCR调节的信号分子调节成牙本质细胞分化和牙本质基质形成。这一假说通过以下具体目标来解决：1）确定包括成牙本质细胞和前成牙本质细胞在内的牙齿间充质细胞中的Gs-coupled GPCR信号如何控制牙本质形成，以及2）确定来自牙齿上皮细胞的Gs-coupled GPCR信号如何调节成牙本质细胞分化。这些目标将采用新开发的G蛋白信号转导矿化组织形成的转基因小鼠模型。在成牙本质细胞和前成牙本质细胞中由I型胶原启动子驱动的Gs偶联GPCR信号增加的转基因小鼠将用于特异性目标1，而在牙上皮细胞中由角蛋白5启动子驱动的Gs偶联GPCR信号增加的小鼠将用于特异性目标2。这些研究将确定GPCR信号通路和其他机制调节成牙本质细胞发育和牙本质基质形成之间的新的相互作用。最终，这些数据将为跨学科研究计划和R 01资助申请奠定基础，以工程师的管状牙本质支持成牙本质细胞和牙髓愈合龋齿的生理复合体。这项工作的知识也将提高我们对遗传性牙齿畸形和环境因素的概念性理解，这些因素是正确的细胞-基质相互作用所必需的，以支持牙本质和其他矿化组织的正常发育。拟议的职业发展和研究活动将在高度支持性的研究密集型环境中进行。两位牙齿发育生物学的国际专家Pamela DenBesten DDS，MS（主要导师）和Ophir Klein MD，PhD（共同导师）将监督Horst博士的研究重点是上皮-间充质相互作用和矿化组织的形成。两位GPCR信号传导领域的国际专家，布鲁斯康克林博士（共同导师，干细胞中的GPCR信号传导）和罗伯特尼森博士（共同导师，骨中的GPCR信号传导），将监督转基因小鼠模型的工作，并将他们与其他干细胞类型和矿化组织的丰富经验相结合，以了解GPCR信号传导在牙齿干细胞和牙本质牙髓复合体形成中的作用。导师都是新的Eli和Edythe广泛的再生医学和干细胞研究中心的成员，该中心将作为培训机会的中心资源（讲习班，研讨会，期刊俱乐部和务虚会），将发育，分子和细胞生物学的专业知识与医学相关的焦点相结合，如本项目中提出的。拟议的研究是一个协调的职业发展计划的一部分，准备候选人通过研究，课程和教程成为一个杰出的，独立的牙医科学家。跨学科导师团队将共同指导职业发展活动，并促进霍斯特博士从目前的研究经验到指导临床科学家发展阶段的自然发展，然后走向独立。