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Harnessing the anabolic potential of Wnt signaling to improve bone health

Harnessing the anabolic potential of Wnt signaling to improve bone health
利用 Wnt 信号的合成代谢潜力来改善骨骼健康
批准号:
10293554
负责人:
ALEXANDER G ROBLING
金额:
$0.0万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-01-01 至 2024-09-30
关键词:
AddressAdultAdverse eventAffectAgeAge-YearsAlcohol consumptionAmericanAwardBasic ScienceBed restBindingBiomechanicsBone DiseasesBone TissueC57BL/6 MouseCardiovascular systemCell LineageCellsComplexCre driverDataDefectDevelopmentDiagnosisDioxinsDiseaseEffector CellEngineeringEnvironmental Risk FactorEnzyme-Linked Immunosorbent AssayErinaceidaeEventExposure toFDA approvedFatty AcidsFatty acid glycerol estersFractureFutureGene ExpressionGenetic TranscriptionGlucocorticoidsGlycoproteinsGoalsHealthHigh PrevalenceHigh Risk WomanHip FracturesHomeostasisHumanInflammatory Bowel DiseasesKnock-outKnockout MiceLabelLigandsLimb BudLong-Term CareLoxP-flanked alleleMarketingMeasuresMechanicsMediatingMesenchymalMethodsModelingMonkeysMusMuscleMutant Strains MiceMutationMyocardial InfarctionOrgan TransplantationOsteoblastsOsteoclastsOsteocytesOsteogenesisOsteopeniaOsteoporosisParalysedPartner in relationshipPathway interactionsPatientsPersonsPharmacologyPhenotypePopulationPost-Traumatic Stress DisordersPostmenopausePre-Clinical ModelPredispositionPrisonerPropertyProteinsRattusRegulationResearchRheumatoid ArthritisRiskRisk FactorsSerum MarkersSerum ProteinsServicesSignal PathwaySignal TransductionSiteSkeletonSmokingSteroidsStrokeTailTetrachlorodibenzodioxinTherapeuticVeteransVietnamWNT Signaling PathwayWarWasting SyndromeWnt proteinsWomanWorkadjudicationagent orangebasebonebone healthbone lossbone massbone metabolismbone preservationcarboxylesterasecardiovascular risk factorcell typecortical boneexperimental studyfracture riskimprovedinhibitorlifestyle factorsmedication safetymenmilitary veteranmortalityneutralizing antibodynovelosteoclastogenesisosteoporosis with pathological fracturephase III trialprogramsradiological imagingreceptorresponseside effectskeletalsuccesstherapy developmenttumorwasting

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英文摘要
Osteoporosis (porous bone disease) is a disease of the skeleton that can have debilitating effects on many US veterans. An estimated 44 million Americans, or 55 percent of the people 50 years of age and older, are currently at risk for osteoporotic fracture. Improved treatment options for the disease require a greater understanding of the cellular events and signaling pathways that control bone metabolism. The proposed research capitalizes on a recently identified secreted inhibitor of Wnt glycoproteins. The long-term goal of the proposed project is to investigate whether targeting a new, secreted inhibitor of Wnt signaling—Notum--can improve bone properties and reduce fracture susceptibility. In the first aim we propose to determine the cell type in which Notum inhibition exerts its effects on bone homeostasis, by crossing conditional Notum mutant mice to different Cre drivers that are active during different stages of the mesenchymal cell lineage. We will also look the gene expression changes induced by Notum inhibition to see if the canonical Wnt pathway, the noncanonical Wnt pathway, the Hedgehog pathway, or some other pathway, is primarily affected. We will also identify downstream nodes in the pathways altered by Notum inhibition, to see if there are more readily targetable effectors of the HBM phenotype induced by Notum inhibition. I the second aim, we will conduct functional studies targeting Notum, which has direct applicability to future therapeutic approaches in patients. Glucocorticoids are widely used among the veteran population for numerous conditions, including organ transplant, rheumatoid arthritis, inflammatory bowel disease, and others, but side effects are not trivial, and bone wasting is a major concern among glucocorticoid-treated patients. Likewise, mechanical disuse is a major problem among veterans, which results from long term bedrest, paralysis, and other complications. We will inhibit Notum in these preclinical models to determine whether Notum inhibition represents a viable strategy for preserving bone mass and function during two relevant bone wasting conditions. In this renewal Merit application, we address these questions in order to identify new ways to improve bone health among the veteran population, and among the public in general.
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ORS Musculoskeletal Biology Workshop at Zermatt
Lrp5 and Lrp6 signaling in bone mechanotransduction and metabolism
Neurogenic bone loss after SCI: skeletal rehabilitation via Wnt and exercise interactions
  • 批准号:
    10507784
  • 项目类别:
  • 资助金额:
    $0.0万
  • 财政年份:
    2021
  • 负责人:
    ALEXANDER G ROBLING
  • 依托单位:
Neurogenic bone loss after SCI: skeletal rehabilitation via Wnt and exercise interactions
  • 批准号:
    10317142
  • 项目类别:
  • 资助金额:
    $0.0万
  • 财政年份:
    2021
  • 负责人:
    ALEXANDER G ROBLING
  • 依托单位:
海外基金