Collagen VI: Novel Mechanisms and Functions in Alzheimer's Disease
Collagen VI: Novel Mechanisms and Functions in Alzheimer's Disease
批准号:
7922089
负责人:
Dena Bou Dubal
金额:
$10.8万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-09-01 至 2014-08-31
关键词:
AddressAgeAgingAlzheimer&aposs DiseaseAlzheimer&aposs disease modelAmyloidAmyloid beta-Protein PrecursorAnimal ModelAtomic Force MicroscopyAutopsyBehaviorBehavioralBindingBiochemicalBiological AssayBrainCell Culture TechniquesCell DeathCell SurvivalCellsCessation of lifeClinicalCognitiveCognitive deficitsCollagenDataDementiaDevelopmentDevelopment PlansDiseaseDoctor of PhilosophyElderlyEmployee StrikesEnvironmentEnzyme-Linked Immunosorbent AssayExposure toExtracellular MatrixExtracellular Matrix ProteinsExtracellular SpaceFamilyFellowshipFunctional disorderGenerationsGenesGoalsHistologyHumanImmunohistochemistryImpaired cognitionIntegrin BindingIntegrinsKnowledgeLaboratoriesLearningLentivirus VectorMAP Kinase GeneMeasuresMediatingMedicineMemoryMentorsMethodsMindModelingMolecularMolecular TargetMusNerve DegenerationNeurodegenerative DisordersNeurologyNeuronsNeurosciencesOrganPathogenesisPathway interactionsPeptidesPeripheralPhysiciansPlayPrincipal InvestigatorProtein BindingProteinsReceptor SignalingResearchResearch InfrastructureResearch PersonnelResearch ProposalsResourcesReverse Transcriptase Polymerase Chain ReactionRodentRoleScientistSenile PlaquesSignal PathwaySignal TransductionStaining methodStainsTechniquesTestingToxic effectToxinTrainingTransgenic MiceViral VectorWagesWestern Blottingaging populationcareercareer developmentcytotoxicdensitydentate gyrusdesigneffective therapyexperienceextracellularfamilial Alzheimer diseasein vivomolecular markermouse modelmutantneuropathologyneuroprotectionnovelpreventprogramsreceptorresearch studyresponseskillssmall hairpin RNAtherapy development
中文摘要
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION (provided by applicant): With the rapid increase in the world's aging population, a cure for neurodegenerative conditions is urgently needed. Alzheimer's disease (AD), the most common disease of memory in the elderly, devastates the minds of millions of people every year. Research over the past decade has revealed that amyloid-¿ (A¿) peptides, soluble toxins, play a central role in the pathogenesis of AD. However, despite our growing knowledge of how AD devastates the brain, there are no effective treatments to prevent or modify the course of the disease. This proposal is aimed at identifying and developing neuroprotective strategies against AD. We propose to investigate novel functions of collagen VI, an extracellular matrix protein, in protection against the deleterious effects of A¿ in the brain. Our preliminary studies show that collagen VI, which is robustly increased in the brain in a mouse model of AD and in human AD, dramatically prevents the toxicity of A¿ in mouse neurons. To extend these findings, in Specific Aim 1, we will examine the extracellular actions of collagen VI, with the goal of determining whether collagen VI binds A¿, alters its assembly, and enhances amyloid plaque formation. In Specific Aim 2, we will investigate intracellular mechanisms of collagen VI- mediated protection to determine whether collagen VI alters the expression of key survival factors to counter A¿ toxicity. In Specific Aim 3, we will focus on the effects of collagen VI on behavior and ascertain whether collagen VI prevents A¿-dependent cognitive dysfunction. Our studies may reveal key protective mechanisms that could serve as direct targets for the development of treatments for AD and other diseases of aging. The candidate is a physician-scientist with a strong commitment to a career in academic medicine focused on identifying strategies to protect against neurodegenerative conditions of aging, such as Alzheimer's disease and related dementias. The candidate has a PhD in neuroscience and an MD with clinical training in neurology and subspecialty training in dementias. The research proposal and career development plan build upon her training in neuroscience, aging, and neurodegenerative conditions to provide expertise in transgenic mouse models of Alzheimer's disease, behavioral analysis, histology, cell culture and viral vectors. The mentoring and research experience described in the proposal would provide resources, salary.
RELEVANCE: Although Alzheimer's disease (AD) devastates the minds of millions of people, there are no truly effective treatments. This proposal is aimed at developing strategies to protect the brain against AD by investigating newfound protective actions of collagen VI, a protein whose effects in the brain are virtually unknown. The mechanisms of this protection may be direct targets for developing effective AD treatments.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Sex Differences in Epigenetic Parent-of-X Origin and Alzheimer's Disease
-
批准号:10525754
-
项目类别:
-
资助金额:$174.38万
-
财政年份:2022
-
负责人:Dena Bou Dubal
-
依托单位:
Mechanisms of X-Chromosome-dependent Sex Difference inAlzheimers Disease
-
批准号:10033567
-
项目类别:
-
资助金额:$226.7万
-
财政年份:2020
-
负责人:Dena Bou Dubal
-
依托单位:
Klotho and Neurodegenerative Disease
-
批准号:9234077
-
项目类别:
-
资助金额:$35.09万
-
财政年份:2016
-
负责人:Dena Bou Dubal
-
依托单位:
Klotho and Neurodegenerative Disease
-
批准号:9107130
-
项目类别:
-
资助金额:$35.08万
-
财政年份:2016
-
负责人:Dena Bou Dubal
-
依托单位:
Klotho and Neurodegenerative Disease
-
批准号:9894866
-
项目类别:
-
资助金额:$34.66万
-
财政年份:2016
-
负责人:Dena Bou Dubal
-
依托单位:
Collagen VI: Novel Mechanisms and Functions in Alzheimer's Disease
-
批准号:8411436
-
项目类别:
-
资助金额:$6.56万
-
财政年份:2009
-
负责人:Dena Bou Dubal
-
依托单位:
Collagen VI: Novel Mechanisms and Functions in Alzheimer's Disease
-
批准号:8318175
-
项目类别:
-
资助金额:$10.8万
-
财政年份:2009
-
负责人:Dena Bou Dubal
-
依托单位:
Collagen VI: Novel Mechanisms and Functions in Alzheimer's Disease
-
批准号:8534006
-
项目类别:
-
资助金额:$10.8万
-
财政年份:2009
-
负责人:Dena Bou Dubal
-
依托单位:
Collagen VI: Novel Mechanisms and Functions in Alzheimer's Disease
-
批准号:7729495
-
项目类别:
-
资助金额:$10.8万
-
财政年份:2009
-
负责人:Dena Bou Dubal
-
依托单位:
Collagen VI: Novel Mechanisms and Functions in Alzheimer's Disease
-
批准号:8124931
-
项目类别:
-
资助金额:$4.24万
-
财政年份:2009
-
负责人:Dena Bou Dubal
-
依托单位:
国内基金
海外基金
登录
查看更多内容
补阳还五汤通过AGE-RAGE通路调控脓毒症免疫失衡的机制与转化研究
-
批准号:JCZRLH202601523
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2026
-
负责人:
-
依托单位:
靶向递送一氧化碳调控AGE-RAGE级联反应促进糖尿病创面愈合研究
-
批准号:JCZRQN202500010
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2025
-
负责人:
-
依托单位:
对香豆酸抑制AGE-RAGE-Ang-1通路改善海马血管生成障碍发挥抗阿尔兹海默病作用
-
批准号:2025JJ70209
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2025
-
负责人:雷芬芳
-
依托单位:
AGE-RAGE通路调控慢性胰腺炎纤维化进程的作用及分子机制
-
批准号:--
-
项目类别:面上项目
-
资助金额:--
-
批准年份:2024
-
负责人:万荣
-
依托单位:
甜茶抑制AGE-RAGE通路增强突触可塑性改善小鼠抑郁样行为
-
批准号:2023JJ50274
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2023
-
负责人:贺志明
-
依托单位:
蒙药额尔敦-乌日勒基础方调控AGE-RAGE信号通路改善术后认知功能障碍研究
-
批准号:--
-
项目类别:地区科学基金项目
-
资助金额:33万元
-
批准年份:2022
-
负责人:都义日
-
依托单位:
补肾健脾祛瘀方调控AGE/RAGE信号通路在再生障碍性贫血骨髓间充质干细胞功能受损的作用与机制研究
-
批准号:--
-
项目类别:面上项目
-
资助金额:52万元
-
批准年份:2022
-
负责人:叶宝东
-
依托单位:
LncRNA GAS5在2型糖尿病动脉粥样硬化中对AGE-RAGE 信号通路上相关基因的调控作用及机制研究
-
批准号:
-
项目类别:省市级项目
-
资助金额:10.0万元
-
批准年份:2022
-
负责人:于海兵
-
依托单位:
围绕GLP1-Arginine-AGE/RAGE轴构建探针组学方法探索大柴胡汤异病同治的效应机制
-
批准号:81973577
-
项目类别:面上项目
-
资助金额:55.0万元
-
批准年份:2019
-
负责人:辛贵忠
-
依托单位:
AGE/RAGE通路microRNA编码基因多态性与2型糖尿病并发冠心病的关联研究
-
批准号:81602908
-
项目类别:青年科学基金项目
-
资助金额:18.0万元
-
批准年份:2016
-
负责人:刘括
-
依托单位: