Role of spatial heterogeneous matrix stifness in development of craniofacial tissue interfaces
Role of spatial heterogeneous matrix stifness in development of craniofacial tissue interfaces
批准号:
9328848
负责人:
Sam Carsten-Puisis Norris
金额:
$4.48万
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-09-07 至 2019-09-06
关键词:
ArthritisBehaviorBiocompatible MaterialsBiological AssayCaliforniaCartilageCell Differentiation processCell LineageCell physiologyCellsChemicalsComplexCuesDegenerative DisorderDentalDevelopmentDevelopmental BiologyDifferentiation AntigensDimensionsEncapsulatedEngineeringEnvironmentExtracellular MatrixHeterogeneityHumanHydrogelsInvestigationLengthLocationLos AngelesMandibular CondyleMechanicsMesenchymal DifferentiationMesenchymal Stem CellsModulusMorphologyNaturePatternPhenotypePhysiologicalPolymersPositioning AttributePropertyReconstructive Surgical ProceduresRegenerative MedicineResearchResearch PersonnelResearch ProposalsResolutionRoleSamplingScientistSeedsStem Cell ResearchStem cellsStructureSurfaceSystemTechniquesTestingTimeTissue EngineeringTissuesTooth structureUniversitiesVariantbasebonecell behaviorcell motilitycraniofacialcraniofacial developmentcrosslinkdensitydesignhigh throughput analysishuman stem cellsin vivoinsightinterestlight intensitymechanical propertiesnovelresponsestem cell fatesubmicronthree dimensional cell culturetool
中文摘要
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英文摘要
Project Summary/Abstract
Research demonstrates that extracellular matrix (ECM) stiffness dictates the differentiation of the mesenchymal
stem cells (MSCs) attached to it. Stiffer substrates promote the differentiation of stiffer cell lineages [1].
Photodegradable hydrogels are a novel class of polymeric biomaterials that have been developed by our group at
University of California, Los Angeles. They are uniquely suited to replicate the ECM[2, 3] and are physically and
chemically similar to the ECM, having a wide range of elastic moduli (~1-500 kPa). Distinctive of
photodegradable hydrogels is that their cross-link density can be altered externally, where stiffness is a function
of the light intensity and exposure time. This biomaterial can replicate complex, anisotropic, and heterogeneous
microenvironments that mimic the structural heterogeneities of native tissue with sub-micron resolutions. This
project proposes to advance tissue engineering through the design and use of this photodegradable hydrogel as
a high-precision advanced biomaterial, with five degrees of control (three spatial dimensions, time and intrinsic
property gradation). I intend to mimic patterns and stiffness gradations found in native tissue interfaces in order
to analyze MSC behavior and advance the understanding of stem cell fate in vivo.
The mechanical patterns I intend to create will ultimately replicate the inherently complex environments found
in nature, such as the developing tooth and the bone-cartilage interface of the mandibular condyle. To date,
ECM-based stem cell research has not replicated the body's polarized structures to a degree that allows for an
understanding of cell fate in such environments. This research proposal intends to establish how heterogeneous
mechanical environments impact MSCs in 2D and 3D culture to subsequently answer the following: Are
microenvironments that contain polarized structures dictating stem cell fate? If we engineer an environment to
mimic native conditions, will stem cells follow suit? Hypothesis: Photo-tunable polymer networks can be used
to structure heterogeneities similar to those found native tissue by inducing a cellular response to mechanical
cues. Since it has been established that cell differentiation can be triggered mechanically in static isotropic
materials, a system with spatial differences in mechanical properties should trigger multiple cell lineages within
a continuous material across a multitude of length and time scales. I also expect that beyond controlling cell
phenotype, intermediate behavior, as found in native tissue interfaces, will be observed.
期刊论文(0)
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科研奖励(0)
会议论文
Spatiotemporal mechanical inhomogeneities in the embryonic oral epithelium and mesenchyme lead to tooth invagination
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批准号:10532673
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项目类别:
-
资助金额:$7.03万
-
财政年份:2020
-
负责人:Sam Carsten-Puisis Norris
-
依托单位:
Spatiotemporal mechanical inhomogeneities in the embryonic oral epithelium and mesenchyme lead to tooth invagination
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批准号:10249181
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项目类别:
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资助金额:$6.8万
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财政年份:2020
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负责人:Sam Carsten-Puisis Norris
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依托单位:
Role of spatial heterogeneous matrix stifness in development of craniofacial tissue interfaces
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批准号:9569268
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项目类别:
-
资助金额:$4.53万
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财政年份:2017
-
负责人:Sam Carsten-Puisis Norris
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依托单位:
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