Regulation of Bone Formation by G-protein Signaling

G 蛋白信号传导调控骨形成

• 批准号: 7842182
• 负责人: EDWARD C HSIAO
• 金额: $ 12.8万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN FRANCISCO
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-07-03 至 2014-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7842182
• 关键词: Accident and Emergency department; Adipocytes; Affect; Agonist; Anabolism; Apoptosis; Biological Process; Bone Diseases; Bone Growth; Bone Marrow; Bone Marrow Cells; Cell Culture Techniques; Cell Shape; Cell model; Clinical; Data; Defect; Development; Development Plans; Disease; Drug Delivery Systems; Engineering; Ensure; Foundations; Fracture; Fracture Healing; Future; G Protein-Coupled Receptor Genes; G-Protein Signaling Pathway; G-Protein-Coupled Receptors; GTP-Binding Proteins; Goals; Health; Heterotopic Ossification; In Vitro; Joints; K-Series Research Career Programs; Ligands; McCune-Albright Syndrome; Mediating; Mentors; Metabolic Bone Diseases; Methods; Modeling; Mus; Musculoskeletal; Musculoskeletal Diseases; Osteoblasts; Osteoclasts; Osteogenesis; Osteoporosis; Paget' s Disease; Pathologic; Phenotype; Physicians; Physiological; Regenerative Medicine; Regulation; Research; Research Design; Research Personnel; Role; Scientist; Signal Transduction; Techniques; Testing; Therapeutic; Tissues; Training; Transgenic Mice; United States; Visit; base; bone; bone loss; bone mass; career; career development; cell population study; cell type; embryonic stem cell; experience; human disease; improved; in vivo; insight; novel; osteoblast differentiation; osteogenic; prevent; programs; receptor; skeletal; skills; tissue culture; tool

DESCRIPTION (provided by applicant): Musculoskeletal disorders affecting the bones and joints are a growing health problem. Osteoporosis affects over 10 million people in the United States. In addition, bone fractures result in over 3 million emergency department visits a year. Since our ability to treat and prevent these diseases is still very rudimentary, elucidating the mechanisms that regulate bone formation is crucial for understanding the pathologic changes in bone diseases and for developing targeted treatments to increase bone formation. The overall objective of this proposal is to define the biological processes regulating the formation of musculoskeletal tissues in a newly developed model of G-protein signaling in bone growth. Prior results showed that expression in osteoblasts of an engineered receptor activated solely by synthetic ligand (RASSL), "Rs1," could dramatically increases bone mass in Rs1 transgenic mice. This proposal will define the basis of this phenotype in three specific aims: 1) determine the cellular mechanisms of Rs1-induced bone formation with a combination of mouse and in vitro tissue culture models; 2) determine how Gs signals affect osteoblast differentiation in mouse and embryonic stem cell models; and 3) identify endogenous GPCRs mimicked by Rs1 using directed expression analysis of Rs1-expressing osteoblasts. Successful completion of these studies will identify new interactions between G-protein signaling pathways and other mechanisms of bone growth, while identifying native GPCRs that may be important clinical targets for increasing bone growth. In addition, the results will improve our understanding of how osteoblasts, adipocytes, and bone marrow interact in normal bone. The proposed research is part of a coordinated career development plan to prepare the candidate to be an outstanding, independent physician-scientist through research, coursework, and tutorials. The candidate will acquire additional training under his mentors' guidance on the utilization of fundamental and translational methods for studying developmental diseases. Finally, a mentoring committee will ensure that the candidate acquires the skills and experience necessary to successfully direct an independent research program by the conclusion of the Career Development Award.

描述（由申请人提供）：影响骨骼和关节的肌肉骨骼疾病是一个日益严重的健康问题。在美国，骨质疏松症影响超过1000万人。此外，骨折每年导致超过300万个急诊室就诊。由于我们治疗和预防这些疾病的能力仍然非常基本，因此阐明调节骨骼形成的机制对于理解骨骼疾病的病理变化和开发靶向治疗以增加骨形成至关重要。该建议的总体目的是定义调节骨骼生长中G蛋白信号传导模型中调节肌肉骨骼组织形成的生物学过程。先前的结果表明，仅通过合成配体（RASSL）激活的工程受体的成骨细胞表达，“ RS1”可以显着增加Rs1转基因小鼠的骨骼质量。该建议将在三个特定目的中定义该表型的基础：1）确定Rs1诱导的骨形成的细胞机制与小鼠和体外组织培养模型的结合； 2）确定GS信号如何影响小鼠和胚胎干细胞模型中成骨细胞分化； 3）使用表达RS1的成骨细胞的定向表达分析来确定由RS1模仿RS1的内源性GPCR。这些研究的成功完成将确定G蛋白信号通路与骨生长的其他机制之间的新相互作用，同时确定可能是增加骨骼生长的重要临床靶标的天然GPCR。此外，结果将提高我们对成骨细胞，脂肪细胞和骨髓如何在正常骨骼中相互作用的理解。拟议的研究是一项协调的职业发展计划的一部分，旨在通过研究，课程和教程使候选人成为一名杰出的独立医师科学家。候选人将在他的导师指导的指导下获得有关研究发育疾病的基本和转化方法的指导。最后，指导委员会将确保候选人通过“职业发展奖”结束，成功地指导独立研究计划所需的技能和经验。