Localization of adenosine to promote fracture healing
Localization of adenosine to promote fracture healing
批准号:
10461465
负责人:
Shyni Varghese
金额:
$50.25万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2022
资助国家:
美国
项目状态:
未结题
起止时间:
2022-09-15 至 2027-05-31
关键词:
ADORA2A geneAcidsAddressAdenosineAdjuvantAgeAgingAnimalsBMP2 geneBehaviorBiocompatible MaterialsBlood CirculationBone DiseasesBone InjuryBone RegenerationBone TissueBone TransplantationBone callusCD8-Positive T-LymphocytesCellsClinicalCyclic AMPDefectDevelopmentDoseEconomic BurdenElderlyEnvironmentFlow CytometryFractureFunctional disorderGaitGene ExpressionHalf-LifeHistologicHyaluronic AcidImmuneImmune responseImpaired healingImplantIn SituInjectableInjuryKnock-outLiteratureMatrix MetalloproteinasesMechanicsModelingMusNatural regenerationNatureOperative Surgical ProceduresOsteogenesisOsteoporosisPatientsPlasmaPlayPopulationPrevalenceProteinsPublic HealthPurinergic P1 ReceptorsQuality of lifeReceptor SignalingRegulatory T-LymphocyteResearchRoleSignal TransductionSiteT-LymphocyteTestingTherapeuticTibial FracturesTissuesTraumaVascularizationWild Type Mouseactive lifestyleage relatedagedangiogenesisbasebonebone agingbone fracture repairbone healingbone healthbone qualitycostcost effectivecrosslinkcytokineextracellularfragility fracturehealingimmunoregulationimprovedjuvenile animallaser capture microdissectionlongitudinal analysismacrophageneutrophilnovel therapeutic interventionolder patientperipheral bloodregenerativerepairedscaffoldsexsingle-cell RNA sequencingspatiotemporalsuccesstissue regenerationtissue repair
中文摘要
摘要
骨折是一种非常常见的损伤,并且随着年龄的增长,
积极生活方式的增加。尽管骨的再生能力,骨损伤往往遭受延迟
愈合或不愈合。骨折的患病率和修复费用正在上升,主要是由于老龄化
的人口。对患者的生活质量和经济负担的深刻负面影响,
创伤或与年龄相关的脆性骨折后的骨折治疗需要开发有效且
具有成本效益的创伤愈合佐剂,以加快愈合速度并提高愈合质量。的
拟议的研究集中在生物材料辅助的腺苷局部递送,以促进老年人的骨愈合。
通过再生内源性组织环境和修复细胞来修复骨组织。我们假设当地
腺苷在损伤部位的递送将诱导促再生免疫环境并促进细胞的再生。
通过增强成骨细胞生成和血管生成使老化骨组织再生。这些假设
将通过以下目标进行测试。目的1将确定腺苷的局部递送的效果,以促进
老年小鼠胫骨横断骨折和临界节段性骨折骨再生的实验研究
股骨缺损目的2将确定腺苷递送在免疫调节中的作用,从而增强
骨再生成功完成拟议的研究将对公共卫生产生重大影响
通过建立一种新的治疗干预来促进骨再生。
英文摘要
ABSTRACT
Bone fracture is a very common injury, and there has been a dramatic increase in trauma-induced fractures with
the increase in active lifestyle. Despite the regenerative ability of bone, bone injuries often suffer from delayed
healing or non-unions. The prevalence of bone fracture and the cost of repair is on the rise primarily due to aging
of the population. The profound negative impact on the patient’s quality of life and the economic burden of
fracture treatment following trauma or age-related fragility fractures warrants the development of efficient and
cost-effective fracture-healing adjuvants to accelerate the healing rate and improve the quality of healing. The
proposed research focuses on biomaterial-assisted local delivery of adenosine to promote bone healing of aged
bone tissues by rejuvenating the endogenous tissue environment and reparative cells. We hypothesize that local
delivery of adenosine at the injury site will induce a pro-regenerative immune environment and promote
regeneration of aging bone tissues through enhanced osteoblastogenesis and angiogenesis. These hypotheses
will be tested through the following aims. Aim 1 will determine the effect of local delivery of adenosine to promote
bone regeneration in aged mice by using two injury models: transverse tibial fracture and critical-sized segmental
femoral defect. Aim 2 will determine the role of adenosine delivery on immunomodulation leading to enhanced
bone regeneration. Successful completion of the proposed studies will have a significant impact in public health
by establishing a new therapeutic intervention for promoting bone regeneration.
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