Democratizing embryo biomechanics: Development of robust and accessible methods to quantify sub-cellular mechanics in vivo
Democratizing embryo biomechanics: Development of robust and accessible methods to quantify sub-cellular mechanics in vivo
批准号:
10724783
负责人:
Jose R Alvarado
金额:
$43.59万
依托单位国家:
美国
项目类别:
财政年份:
2023
资助国家:
美国
项目状态:
未结题
起止时间:
2023-09-02 至 2025-08-31
关键词:
ActomyosinAddressAnimalsAtomic Force MicroscopyBenchmarkingBiologicalBiomechanicsCell membraneCellsCellular biologyCommunitiesComputers and Advanced InstrumentationCongenital AbnormalityCytoplasmDataDefectDevelopmentEmbryoEmbryonic DevelopmentEngineeringGoalsHeterogeneityHumanIntercellular JunctionsLabelLasersLinkMagnetismMammalsMeasurementMeasuresMechanicsMembraneMethodsMicrodissectionMicroscopeMolecularMorphogenesisMotionNatureOrangesOrganPatternPhasePhysicsPhysiologic pulsePropertyProtein DynamicsProteinsReporterResearch PersonnelResolutionRheologySamplingSystemTechnologyTimeTissuesTwin Multiple BirthViscosityWorkbiomechanical testcell behaviorcell cortexcell motilitycell typeconvergent extensiondriving behaviorembryo tissueferrofluidfluorescence imagingimprovedin vivoinnovationmechanical forcemechanical propertiesnovelparticleplanar cell polaritysuccesstemporal measurementtoolvertebrate embryos
中文摘要
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英文摘要
Abstract:
It is now widely recognized that any comprehensive understanding of morphogenesis will
require careful quantification of mechanical forces in vivo. However, twin challenges stand in our
way: First, we currently possess only a sparse sampling of subcellular mechanics in embryos, in
part because such analyses are limited by the need for advanced instrumentation. Second,
most analyses of mechanical properties do not provide sufficient spatial resolution to quantify
localized mechanical heterogeneities in discrete sub-regions of the cell. Here, we attack both
problems by developing robust methods for non-invasive quantification of the mechanical
properties of both cell-cell junctions and the cytoplasm. The proposal will develop these tools in
the context of vertebrate embryo axis elongation, but both methods should be widely accessible,
requiring only fluorescent reporters and standard microscopes. Success of the project would 1)
improve our depth of understanding through their high spatial and time resolution and their non-
invasive nature and 2) improve our breadth of understanding by making quantitative
biomechanical analysis in embryos far more accessible to a wide range of investigators.
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