VISCOELASTIC PROPERTIES OF NORMAL AND OA CHONDRONS
VISCOELASTIC PROPERTIES OF NORMAL AND OA CHONDRONS
批准号:
7172926
负责人:
Farshid Guilak
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
项目状态:
已结题
起止时间:
1998-01-01 至 2008-02-29
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
中文摘要
点击翻译按钮获取中文摘要
英文摘要
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.
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海外基金