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: 8721402
• 负责人: Mia M Thi
• 金额: $ 36.32万
• 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 2015-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8721402
• 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.

描述（由申请人提供）：胰岛素依赖型糖尿病（IDDM； 1型糖尿病）患者骨质流失较高，骨质疏松和相关骨折的风险增加。然而，IDDM中骨质流失的机制尚不完全清楚。骨重塑是一个由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。骨重塑受身体活动对骨骼持续施加的机械刺激的调节，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至关重要。本R01应用的主要目的是验证一个新的假设，即骨机械感觉和转导系统组分的表达改变是导致IDDM中骨细胞功能障碍和骨质流失增加的核心机制。为此，我们将使用骨细胞系进行全面的体外研究，将独特地结合体内骨生理学和1型糖尿病秋田小鼠模型的原位骨组织分析。提出的体外研究将为高葡萄糖对骨细胞检测和机械刺激反应的影响提供机制见解。在体内和最终的原位研究中，对照年龄匹配小鼠和秋田小鼠接受胰岛素治疗或不接受胰岛素治疗，将确定糖尿病和相关的高葡萄糖对机械负荷下骨形成的影响，并评估改变的骨机械信号对糖尿病骨质流失的贡献。这些研究将由一位具有生物医学工程背景的新研究员指导，他已经开始了骨科外科的第一个教员任命。研究将结合生物医学工程、药理学、生理学和分子生物学领域的初级和高级研究人员的广泛专业知识，以及最先进的生物化学、活细胞成像、组织形态学研究和无创体内全动物骨成像。这些建议的研究不仅有望促进对糖尿病性骨质减少的机制的理解，强调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控制血糖对预防和逆转糖尿病骨质流失的重要性。