Mutant tubulins confer resistance to pathological tau
Mutant tubulins confer resistance to pathological tau
批准号:
10461943
负责人:
Sarah Jean Zimmerman Benbow
金额:
$12.74万
依托单位:
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:
2021-08-15 至 2024-02-29
关键词:
AddressAffectAlzheimer&aposs DiseaseAxonal TransportBehavioralBindingBiochemicalBiology of AgingCaenorhabditis elegansClinicalClustered Regularly Interspaced Short Palindromic RepeatsCommunitiesCytoskeletonDefectDevelopmentDiseaseDisease ProgressionFrontotemporal Lobar DegenerationsGenesGoalsHealthcare SystemsHumanIn VitroJournalsKnowledgeLaboratoriesLeadershipMAPT geneMeasuresMediatingMedicalMethodsMicrotubule PolymerizationMicrotubulesModelingMolecularMotorMutant Strains MiceMutationNerve DegenerationNeurodegenerative DisordersNeuronal DysfunctionNeuronsPathologicPathologyPhasePhenotypePhosphorylationPlayPoint MutationPrevalencePrincipal InvestigatorProcessPropertyProteinsResearchResearch PersonnelResistanceResourcesRoleSystemTauopathiesTestingToxic effectTrainingTransgenic OrganismsTranslatingTranslationsTubulinUnited States Department of Veterans AffairsUniversitiesWashingtonWorkage relatedaging populationbasebiophysical techniquescareercareer networkingcell motilitychronic traumatic encephalopathyexperimental studygain of functiongenetic approachhealth care economicsimprovedinterestlive cell imagingmeetingsmutantnew therapeutic targetnovel therapeutic interventionprotein aggregationreconstitutionskillssocialsoundtau Proteinstau aggregationtau-microtubule interaction
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英文摘要
Project Summary/Abstract
Pathological tau is present in a number of age-related diseases (tauopathies) including
Alzheimer's Disease (AD). With a rising aged population the prevalence of these diseases will
become an enormous healthcare, economic and social burden. To-date there are no clinically
proven disease altering treatments. Recently, we have discovered mutant tubulin modifies
tauopathy-like phenotypes in transgenic C. elegans models, reducing human tau-induced motility
deficits and neurodegeneration. We hypothesize that mutant tubulin ameliorates tau-induced
phenotypes in C. elegans by altering tau-microtubule interactions. To test our hypothesis we
propose to 1) use C. elegans to determine if the level of tubulin suppression is based in tubulin
expression level 2) use reconstituted in vitro systems to test whether tubulin mutations affect tau-
microtubule interactions and 3) use mammalian primary neurons to test whether mutant tubulin
impacts microtubule properties and function. The proposed projects will elucidate the
mechanisms of mutant tubulin suppression of tau induced-pathology and tau-microtubule
interactions. Additionally, this work will contribute greater understanding of the cytoskeleton in
neurodegenerative disease.
My goal is to develop a career as a principal investigator devoted to the discovery of the
molecular mechanisms underpinning tauopathies and the roles the cytoskeletal network play in
neurodegeneration. To accomplish this, my training plan focuses on 1) expanding my technical
toolkit to incorporate biophysical approaches and live cell imaging 2) gaining greater knowledge
in the biology of aging 3) improving skills in laboratory leadership and expanding my professional
network.
The University of Washington and the Veterans Affairs Puget Sound Health Care System
share an abundance of researchers interested in Alzheimer's and other neurodegenerative
conditions. There are substantial intellectual resources such as seminars, journal clubs and
meetings that create numerous opportunities broaden my perspective through interactions with
the medical and scientific community in AD-related research.
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Mutant tubulins confer resistance to pathological tau
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批准号:10283016
-
项目类别:
-
资助金额:$12.74万
-
财政年份:2021
-
负责人:Sarah Jean Zimmerman Benbow
-
依托单位:
海外基金