Beta-catenin biology in regeneration of uterine smooth muscle
Beta-catenin biology in regeneration of uterine smooth muscle
批准号:
7579120
负责人:
JOSE M. TEIXEIRA
金额:
$31.69万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-03-02 至 2012-12-31
关键词:
ActinsAdherens JunctionAdhesionsAdipocytesAdipose tissueAdultBenignBiologyBone MarrowBone Marrow CellsCadherinsCell NucleusCellsCharacteristicsComplexCytoskeletonDevelopmentDuct (organ) structureDyesEndometrialEndometriumEpitheliumEstrous CycleEtiologyFamilyFatty acid glycerol estersFemale Genital NeoplasmsFlow CytometryGene ExpressionGenesHumanHysterectomyKnowledgeLeadLeiomyomaLinkMediatingMedicalMesenchymeMolecularMusMuscleMuscle CellsMyometrialNatural regenerationNuclearOperative Surgical ProceduresPathologyPathway interactionsPhenotypePlayPregnancyPrimary Cell CulturesProcessProtein IsoformsReportingRoleSignal TransductionSkeletal MuscleSkeletal Muscle Satellite CellsSmooth MuscleSmooth Muscle MyocytesSourceStem cellsStressStructure of paramesonephric ductTCF Transcription FactorTissuesTubeUterine FibroidsUterusWomanadipocyte differentiationbasebeta cateninmembermyogenesismyometriumpostnatalprecursor cellprogenitorregenerativerepairedresidencesatellite celltumoruterine smooth muscle cell
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Although the uterus is indispensable for propagation, and thus survival, of mammalian species, its differentiation from the primordial Mullerian ducts is not well understood. We hypothesize that 2-catenin plays a major role in postnatal uterine development and that its dysregulated function may be an underlying cause of leiomyomata, the most common gynecologic tumor. Conventional Wnt- mediated signal transduction occurs by the stabilization of 2-catenin and its translocation to the nucleus and interaction with the transcription factors TCF/LEF to modulate target gene expression. Additionally, 2-catenin plays an essential role in linking adherens junctions with the actin cytoskeleton. We are investigating the function of 2-catenin in uterine development and have found that targeted deletion of 2-catenin in mouse uterus leads to progressive replacement of smooth muscle with fat in the myometrium with estrous cycling. These results suggested that there is a regenerative cell in the uterus that is dependent on 2-catenin function and is hormonally regulated. We propose to continue these studies by- (I) Identifying the uterine smooth muscle cells that behave like the regenerative satellite cells in skeletal muscle. (II) Determining the source of the cells that contribute to uterine smooth muscle. (III) Determining whether the muscle-fat phenotype is due to the adhesion or the nuclear function of 2-catenin. The results of these studies will provide a better understanding of postnatal uterine development and should provide clues to the etiology of uterine muscle pathologies such a leiomyomata, which are more commonly known as uterine fibroids.
More knowledge is needed about the process of uterine development and function, particularly when these processes are perturbed as with uterine fibroids, a significant indicator for hysterectomy. Understanding the mechanisms governing development of these benign tumors in the uterus should lead to safe, long-term medical therapies based on scientific rationales that could benefit thousands of women annually who might be spared surgery.
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财政年份:2013
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资助金额:$38.05万
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Uterine Leiomyoma Development in Mouse Models
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财政年份:2013
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Endocrine disruption of myometrial stem cell activities
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资助金额:$37.98万
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Endocrine disruption of myometrial stem cell activities
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财政年份:2012
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依托单位:
Uterine-specific genetic modification and lymphangioleiomyomatosis
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项目类别:
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依托单位:
Uterine-specific genetic modification and lymphangioleiomyomatosis
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财政年份:2011
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负责人:JOSE M. TEIXEIRA
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依托单位:
海外基金