Mesenchymal stem cells and the microenvironment

间充质干细胞和微环境

• 批准号: 7413340
• 负责人: CHRISTOPHER S CHEN
• 金额: $ 28.36万
• 依托单位: UNIVERSITY OF PENNSYLVANIA
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-05-01 至 2010-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7413340
• 关键词: Actins; Adhesions; Adhesives; Adipocytes; Adult; Animal Model; Binding; Blood Vessels; Bone and Cartilage Funding; Cell Adhesion; Cell Differentiation process; Cell Lineage; Cells; Cellular Morphology; Cellular biology; Chondrocytes; Connective Tissue; Cues; Cytoskeleton; Degenerative Disorder; Disease; Extracellular Matrix; Fatty acid glycerol esters; Fibroblasts; Fibronectins; Foundations; Goals; Growth Factor; Healed; Health; Homeostasis; Human; Human body; Implant; Integrin-mediated Cell Adhesion Pathway; Integrins; Maintenance; Mechanics; Mesenchymal Stem Cells; Molecular; Multipotent Stem Cells; Muscle; Muscle Cells; Musculoskeletal; Osteoblasts; Osteoporosis; Pathway interactions; Physical environment; Play; Population; Process; Regulation; Research; Research Personnel; Role; Signal Pathway; Signal Transduction; Stem cells; System; Tissues; Work; base; bone; calcification; daughter cell; extracellular; healing; in vivo; injured; insight; multipotent cell; novel; precursor cell; response; rho; stem cell fate

DESCRIPTION (provided by applicant): Human mesenchymal stem cells (MSCs) are multipotent stem cells that differentiate into many of the cells resident in musculoskeletal and stromal tissues of the human body, including fibroblasts, chondrocytes, osteoblasts, myocytes, and adipocytes. While differentiation of the MSCs into appropriate lineages may enhance healing of injured tissues, inappropriate lineage specification may be responsible for numerous pathophysiologic processes, including the decreased bone and increased fat in osteoporotic bones, and the calcification of atherosclerotic vessel walls. Regulation of the lineage commitment of MSCs by local microenvironmental cues therefore may be critical to our fundamental understanding of numerous degenerative as well as healing processes. The long term objective of this research is to characterize the cues within the local surrounding microenvironment that drive the lineage specification and differentiation of human mesenchymal stem cells (MSCs), and the molecular pathways involved. The investigator has recently discovered that adhesion of MSCs to fibronectin regulates a commitment switch in the MSCs between adipogenic and osteogenic lineage specification, through a mechanism involving RhoA signaling and cytoskeletal tension. In this proposal, the investigator proposes to further characterize how adhesive and mechanical cues regulate the commitment of MSCs to osteogenic and adipogenic lineages. Specific Aim 1 will be to investigate the role of integrin-mediated cell adhesion in modulating mesenchymal stem cell commitment by characterizing the binding interactions that drive the MSC lineage commitment switch between osteoblasts and adipocytes. Specific Aim 2 will be to investigate the coordination of RhoA and cytoskeletal tension in the regulation of stem cell commitment. Specific Aim 3 will be to investigate the ability of RhoA to regulate stem cell commitment and differentiation in an animal model. Together, these studies will define roles of cell adhesion, RhoA, and cytoskeletal tension in MSC lineage commitment, and establish a molecular basis for the regulation of MSC differentiation by microenvironmental cues.

描述（由申请人提供）：人间充质干细胞（MSC）是多能干细胞，可分化为人体肌肉骨骼和基质组织中的许多细胞，包括成纤维细胞、软骨细胞、成骨细胞、肌细胞和脂肪细胞。虽然MSC分化成适当的谱系可以促进损伤组织的愈合，但不适当的谱系特异性可能导致许多病理生理过程，包括骨质疏松骨中的骨减少和脂肪增加，以及动脉粥样硬化血管壁的钙化。因此，通过局部微环境线索调节MSC的谱系承诺可能对我们对许多退行性疾病以及愈合过程的基本理解至关重要。本研究的长期目标是表征驱动人类间充质干细胞（MSC）谱系特化和分化的局部周围微环境中的线索，以及所涉及的分子途径。研究人员最近发现，MSC与纤连蛋白的粘附通过涉及RhoA信号传导和细胞骨架张力的机制调节MSC在成脂和成骨谱系特化之间的承诺转换。在这个提议中，研究者建议进一步表征粘附和机械线索如何调节MSC向成骨和成脂谱系的承诺。具体目标1将调查整合素介导的细胞粘附在调节间充质干细胞承诺的作用，通过表征驱动成骨细胞和脂肪细胞之间的MSC谱系承诺转换的结合相互作用。具体目标2将是研究RhoA和细胞骨架张力在干细胞定向调控中的协调作用。具体目标3将是研究RhoA在动物模型中调节干细胞定型和分化的能力。总之，这些研究将确定细胞粘附，RhoA和细胞骨架张力在MSC谱系定型中的作用，并建立微环境因子调控MSC分化的分子基础。