Effects of High Glucose on Bone Cell Mechanosensing, Transduction, and Signaling

高葡萄糖对骨细胞机械传感、转导和信号传导的影响

• 批准号: 8238259
• 负责人: Mia M Thi
• 金额: $ 36.14万
• 依托单位: ALBERT EINSTEIN COLLEGE OF MEDICINE
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-09-20 至 2016-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8238259
• 关键词: Accounting; Adverse effects; Age; Animals; Appointment; Area; Awareness; Biochemical; Biological Assay; Bioluminescence; Biomedical Engineering; Bone Tissue; Bone remodeling; Cell Line; Cells; Cellular Mechanotransduction; Confocal Microscopy; Detection; Development; Diabetes Mellitus; Diabetic mouse; Dinoprostone; Dose; Dyes; Electron Microscopy; Enzyme-Linked Immunosorbent Assay; Exposure to; Faculty; Forelimb; Fracture; Functional disorder; Glucose; Goals; Hyperglycemia; In Situ; In Vitro; Insulin; Insulin-Dependent Diabetes Mellitus; Life; Liquid substance; Luciferases; Maintenance; Measures; Mechanics; Mediating; Molecular Biology; Mus; Orthopedic Surgery procedures; Osteoblasts; Osteoclasts; Osteocytes; Osteogenesis; Osteopenia; Osteoporosis; P2X-receptor; Patients; Pharmacology; Phenotype; Physical activity; Physiology; Process; Purinoceptor; Relative (related person); Research Personnel; Risk; Risk Factors; Signal Transduction; Simulate; Skeleton; Staging; Stimulus; Structure; System; Testing; Thick; Time; bone; bone cell; bone imaging; bone loss; bone mass; cellular imaging; design; diabetic; extracellular; glycemic control; high risk; in vivo; insight; insulin dependent diabetes mellitus onset; luciferin; mRNA Expression; mouse model; novel; prevent; protein expression; receptor; research study; response; shear stress; skeletal; type I diabetic; uptake

DESCRIPTION (provided by applicant): Patients with insulin dependent diabetes mellitus (IDDM; Type 1 diabetes) display higher bone loss and increased risk for osteoporosis and related bone fractures. However, the mechanisms that underlie bone loss in IDDM are still not fully understood. It is well established that bone mass is maintained by bone remodeling, a process that involves formation of new bone by osteoblasts and osteocytes and resorption of existing bone by osteoclasts. Bone remodeling is regulated by mechanical stimuli imposed continuously to the skeleton by physical activity, and proper response of osteocytes/osteoblasts to mechanical loading is thus essential for maintenance of bone function and skeletal integrity. The main goal of this R01 application is to test the novel hypothesis that altered expression of components of bone mechanosensory and transduction systems is a central mechanism leading to bone cell dysfunction and higher bone loss in IDDM. For this we will use comprehensive in vitro studies with bone cell lines that will be uniquely combined with in vivo bone physiology and in situ bone tissue analysis on the Type 1 diabetic Akita mouse model. The proposed in vitro studies will provide mechanistic insights into effects of high glucose on bone cell detection and response to mechanical stimuli. The in vivo and ultimate in situ studies with control age- matched and Akita mice treated with or without insulin will determine the impact of diabetes and associated high glucose on bone formation in response to mechanical loading, and evaluate the contribution of altered bone mechanosignaling to the higher bone loss in diabetes. These studies will be directed by a new investigator who has a background in biomedical engineering and has begun a first faculty appointment in a Department of Orthopaedic Surgery. Studies will combine the broad expertise of junior and senior researchers in the areas of biomedical engineering, pharmacology, physiology and molecular biology, and state-of-the-art biochemical, live cell imaging, histomorphometric studies and non-invasive in vivo whole animal bone imaging. The proposed studies are not only expected to advance understanding of mechanisms underlying diabetic osteopenia, highlighting the deleterious effects of high glucose on bone mechanosensory/transduction systems, but will also bring awareness to the importance of an early and tight glycemic control to prevent and reverse bone loss in diabetes. PUBLIC HEALTH RELEVANCE: Diabetes mellitus is associated with increased bone loss and risk for osteoporosis and bone fracture. The proposed studies will investigate a novel mechanism to explain diabetic osteopenia. If successful, they will not only markedly advance our understanding of mechanisms underlying bone loss in diabetes but will also bring awareness to the importance of an early and tight glycemic control to prevent and reverse diabetic osteopenia.

描述（由申请人提供）：胰岛素依赖型糖尿病（IDDM; 1型糖尿病）患者表现出较高的骨丢失，骨质疏松症和相关骨折的风险增加。然而，胰岛素依赖型糖尿病骨丢失的机制仍不完全清楚。众所周知，骨量是通过骨重建来维持的，骨重建是一个涉及成骨细胞和骨细胞形成新骨以及破骨细胞吸收现有骨的过程。骨重建是由身体活动连续施加到骨骼的机械刺激调节的，因此骨细胞/成骨细胞对机械负荷的适当反应对于维持骨功能和骨骼完整性是必不可少的。该R 01应用的主要目标是测试新的假设，即骨机械感觉和转导系统的组分的表达改变是导致IDDM中骨细胞功能障碍和更高的骨丢失的中心机制。为此，我们将使用骨细胞系的全面体外研究，这些研究将独特地结合1型糖尿病秋田小鼠模型的体内骨生理学和原位骨组织分析。拟议的体外研究将提供机制的见解高葡萄糖对骨细胞检测和响应机械刺激的影响。用对照年龄匹配的小鼠和用或不用胰岛素治疗的秋田小鼠进行的体内和最终原位研究将确定糖尿病和相关的高葡萄糖对响应于机械负荷的骨形成的影响，并评价改变的骨机械信号传导对糖尿病中较高骨损失的贡献。这些研究将由一名新的研究人员指导，该研究人员具有生物医学工程背景，并已开始在矫形外科部门进行首次教师任命。研究将结合联合收割机初级和高级研究人员在生物医学工程，药理学，生理学和分子生物学领域的广泛专业知识，以及最先进的生物化学，活细胞成像，组织形态学研究和非侵入性体内全动物骨成像。拟议的研究不仅有望促进对糖尿病骨质减少机制的理解，突出高葡萄糖对骨机械感觉/转导系统的有害影响，而且还将使人们认识到早期和严格的血糖控制对预防和逆转糖尿病骨质流失的重要性。 公共卫生相关性：糖尿病与骨质流失增加以及骨质疏松症和骨折风险相关。拟议的研究将调查一种新的机制来解释糖尿病骨质减少。如果成功，他们不仅将显着推进我们对糖尿病骨丢失机制的理解，而且还将提高对早期和严格血糖控制的重要性的认识，以预防和逆转糖尿病骨质减少。