VISCOELASTIC PROPERTIES OF NORMAL AND OA CHONDRONS
正常软骨和 OA 软骨的粘弹性特性
基本信息
- 批准号:7172926
- 负责人:
- 金额:$ 32.85万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1998
- 资助国家:美国
- 起止时间:1998-01-01 至 2008-02-29
- 项目状态:已结题
- 来源:
- 关键词:AbbreviationsAdultAffectAlginatesAnabolismAnimalsAtomic Force MicroscopyBehaviorBiochemicalBiomechanicsCartilageCellsCharacteristicsChondrocytesCollagenCollagen Type VIComplexConditionConfocal MicroscopyDegenerative polyarthritisDevelopmentDiffusionElementsEnvironmentEnvironmental Risk FactorEquilibriumExhibitsExtracellular MatrixFinite Element AnalysisFluorescence Recovery After PhotobleachingFundingGoalsHealthHistologyIn SituInterventionJointsKnock-outLeadLiver Acinus Zone 3MeasurementMeasuresMechanical StressMechanicsMediatingMetabolicMicroscopyModelingMolecularMusOperative Surgical ProceduresOsteoarthrosis DeformansPathway interactionsPharmacologic SubstancePlayPropertyProteoglycanRateRegulationRoleSignal TransductionSiteStagingStressStructureTechniquesTestingTheoretical modelTissuesTransgenic MiceTransport Processarticular cartilagecartilage metabolismimprovedmacromoleculenovelphysical propertyresearch studyresponsesizewasting
项目摘要
The mechanical environment of the chondrocytes is an important factor that affects the health and
function of the diarthrodial joint. The mechanical signals to which chondrocytes are exposed depend on
the biomechanical interactions between the cell, pericellular matrix, and extracellular matrix. Currently,
there is little or no information available on the mechanical properties of the pericellular matrix of articular
cartilage. The goals of this study are to measure the intrinsic biomechanical and diffusion properties of
the chondrocyte pericellular matrix, and to test the hypothesis that these properties are altered in
osteoarthritic cartilage. Furthermore, we propose that type VI collagen, which is abundantly present in
the pericellular matrix, influences the physical properties of this region. We will use several novel
experimental techniques to quantify the micromechanical behavior of pericellular matrix using the isolated
_hondron model. The specific aims of this study are: 1) Measure the mechanical properties of the
3ericellular matrix from normal and osteoarthritic cartilage using micropipette aspiration and atomic force
microscopy, incorporate these findings in a theoretical model of cell-matrix interactions in cartilage, and
validate these predictions using 3D confocal microscopy; 2) Measure the diffusion properties of the
pericellular matrix of normal and OA cartilage; 3) Determine how the presence of a normal or OA
pericellular matrix influences the metabolic response of chondrocytes to dynamic compression within an
lartificial matrix; and 4) Determine what role type VI collagen plays in the mechanical properties of the
pericellular matrix. The long-term goals of this study are to improve our understanding of the role of
mechanical factors in the regulation of cartilage metabolism in normal and diseased conditions. A better
understanding of these pathways will hopefully lead to the development of new pharmaceutical or
biophysical interventions for the treatment of osteoarthritis.
软骨细胞的力学环境是影响其健康和健康的重要因素。
腹股沟关节的功能。软骨细胞所暴露的机械信号取决于
细胞、细胞周围基质和细胞外基质之间的生物力学相互作用。目前,
有关关节细胞周围基质的力学性质的信息很少或根本没有。
软骨。本研究的目的是测量内固定材料的内在生物力学和扩散特性。
软骨细胞细胞周围基质,并检验这些特性在
骨关节炎软骨。此外,我们提出了VI型胶原,它丰富地存在于
细胞周围基质,影响这一区域的物理性质。我们将用几本小说
细胞外基质微观力学行为量化的实验技术
_洪德龙模型。本研究的具体目的是:1)测量材料的力学性能
3用微管抽吸法和原子力法从正常软骨和骨关节病软骨中提取细胞基质
显微镜下,将这些发现纳入软骨细胞-基质相互作用的理论模型中,并且
使用3D共聚焦显微镜验证这些预测;2)测量
正常软骨和骨性关节炎的细胞外基质;3)确定正常或骨性关节炎的存在
细胞外基质影响软骨细胞对动态压缩的代谢反应
以及4)确定VI型胶原在血管内皮细胞的力学性能中所起的作用
细胞周围基质。这项研究的长期目标是提高我们对
在正常和疾病条件下软骨代谢调节中的力学因素。更好的
对这些途径的理解将有望导致新的药物或
治疗骨性关节炎的生物物理干预。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Farshid Guilak其他文献
Farshid Guilak的其他文献
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{{ truncateString('Farshid Guilak', 18)}}的其他基金
Synthetic Chronogenetic Gene Circuits for Circadian Cell Therapies
用于昼夜节律细胞疗法的合成计时基因电路
- 批准号:
10797183 - 财政年份:2023
- 资助金额:
$ 32.85万 - 项目类别:
2023 Cartilage Biology and Pathology Gordon Research Conference and Gordon Research Seminar
2023年软骨生物学与病理学戈登研究会议暨戈登研究研讨会
- 批准号:
10605625 - 财政年份:2022
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Genome and epigenome editing of induced pluripotent stem cells for investigating osteoarthritis risk alleles
诱导多能干细胞的基因组和表观基因组编辑用于研究骨关节炎风险等位基因
- 批准号:
10532032 - 财政年份:2022
- 资助金额:
$ 32.85万 - 项目类别:
Deconstructing Cartilage Mechanotransduction by Piezo Channels
通过压电通道解构软骨机械传导
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10533155 - 财政年份:2022
- 资助金额:
$ 32.85万 - 项目类别:
SMART stem cells that autonomously down-modulate TFG-β signaling for Articular Cartilage Repair
SMART 干细胞自主下调 TFG-β 信号传导以修复关节软骨
- 批准号:
10371823 - 财政年份:2022
- 资助金额:
$ 32.85万 - 项目类别:
Genome and epigenome editing of induced pluripotent stem cells for investigating osteoarthritis risk alleles
诱导多能干细胞的基因组和表观基因组编辑用于研究骨关节炎风险等位基因
- 批准号:
10707979 - 财政年份:2022
- 资助金额:
$ 32.85万 - 项目类别:
Genetically-engineered stem cells for self-regulating arthritis therapy
用于自我调节关节炎治疗的基因工程干细胞
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10630757 - 财政年份:2022
- 资助金额:
$ 32.85万 - 项目类别:
Genetically-engineered stem cells for self-regulating arthritis therapy
用于自我调节关节炎治疗的基因工程干细胞
- 批准号:
10598619 - 财政年份:2022
- 资助金额:
$ 32.85万 - 项目类别:
Genetically-engineered stem cells for self-regulating arthritis therapy
用于自我调节关节炎治疗的基因工程干细胞
- 批准号:
10434316 - 财政年份:2022
- 资助金额:
$ 32.85万 - 项目类别:
SMART stem cells that autonomously down-modulate TFG-β signaling for Articular Cartilage Repair
SMART 干细胞自主下调 TFG-β 信号传导以修复关节软骨
- 批准号:
10590752 - 财政年份:2022
- 资助金额:
$ 32.85万 - 项目类别:
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