The role of mesoderm in regulating cell polarity and adhesion during neural crest cell migration. Supplement
The role of mesoderm in regulating cell polarity and adhesion during neural crest cell migration. Supplement
批准号:
10403890
负责人:
Ezra Lencer
金额:
$3.43万
依托单位国家:
美国
项目类别:
财政年份:
2021
资助国家:
美国
项目状态:
已结题
起止时间:
2021-09-01 至 2022-02-28
关键词:
AdhesionsAdultAffectBindingBiosensorCell AdhesionCell Adhesion MoleculesCell PolarityCellsCharacteristicsCleft LipCollagenComplexCongenital MegacolonDataDefectDepositionDevelopmentDevelopmental BiologyDorsalEmbryoEnvironmentEtiologyEventExtracellular MatrixFibronectinsFishesGeneticGoalsHeadHereditary DiseaseImageIn VitroIntegrinsIntrinsic factorKnowledgeLamininMediatingMesodermModificationMolecularMovementMuscleMutationN-CadherinNeoplasm MetastasisNeural CrestNeural Crest CellNeural tubePathway interactionsPeptidesPeripheralPhenocopyPhenotypePigmentation physiologic functionPopulationRegulationResearchRoleRouteSeriesSignal TransductionSpecific qualifier valueStreamSuggestionSurfaceTestingTissuesTransplantationVertebratesZebrafishbonecell motilityexperimental studyin vivoinsightlive cell imagingmigrationmutantprogramsrhotheoriestraitvertebrate embryos
中文摘要
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英文摘要
Abstract
Central to study of development is understanding how morphogenetic movements are regulated. This question
has special bearing for the vertebrate neural crest, a multipotent population of cells that famously migrate in
collective streams from the dorsal neural tube along conserved pathways during development. While much
current theory focuses on cell autonomous factors regulating neural crest cell state, neural crest cell (NCC)
migration is also known to require interactions and integration across different tissues. The overarching goal of
this project is to understand how NCCs integrate internal cell state with external signals from the local cellular
environment to coordinate directed migration. The proposed research will study this problem in zebrafish
where trunk NCC migration depends critically on a population of somitic mesoderm called adaxial cells. Loss of
adaxial cells results in NCC phenotypes suggestive of cell polarity and adhesion defects. Remarkably, adaxial
cells also migrate during development, and NCC migration may be related to adaxial cell migration. Despite the
importance of adaxial cells for NCC migration, the mechanisms underlying this interaction are unknown. The
propose research will test the hypothesis that NCCs require adaxial cells for regulation of cell polarity, and that
that this interaction is mediated through modifications to the extracellular matrix that occurs during adaxial cell
migration. These data will provide insight into a regulatory mechanism controlling zebrafish NCC migration, a
major morphogenetic event that occurs in every vertebrate embryo.
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