The integrated stress response in cognitive disorders
The integrated stress response in cognitive disorders
批准号:
10393550
负责人:
Mauro Costa-Mattioli
金额:
$89.02万
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:
未结题
起止时间:
2012-03-15 至 2026-03-31
关键词:
Animal ModelAutomobile DrivingBehaviorBehavioralBiologicalBiological AssayBiologyBrainCRISPR/Cas technologyChemicalsCognition DisordersDevelopmentDiseaseDissectionEconomicsElectrophysiology (science)ExhibitsGenesGeneticGenetic ModelsGenetic TranslationGenomicsGoalsGrowthHumanImpaired cognitionImpairmentIncidenceIndividualIntellectual functioning disabilityKnowledgeLeadLightMammalian CellMediatingMemory DisordersMemory impairmentMissense MutationModelingMolecularMolecular BiologyMolecular GeneticsMonitorMusMutationNeurodegenerative DisordersNeurogliaPathogenesisPathway interactionsPharmacologyPhosphotransferasesProtein BiosynthesisPublic HealthReporterRoleSignal TransductionSynapsesSynaptic plasticityTestingTranslationsYeastsbasebehavioral studybiological adaptation to stressbrain cellcell growthcell typedesigndrug discoveryeffective therapyexcitatory neuronexperimental studygenetic approachgenome sequencinghigh throughput screeningin vivoinhibitorinhibitory neuroninsightinterdisciplinary approachlong term memoryloss of functionmouse geneticsmouse modelnovelnovel therapeutic interventionnovel therapeuticsprogramsproteostasisribosome profilingscreeningsingle-cell RNA sequencingsmall molecule inhibitorsocialsynaptic functiontoolwhole genome
中文摘要
摘要
英文摘要
ABSTRACT
Cognitive disorders pose a major threat to public health, and represent an enormous economic and social
burden. Despite the high incidence of these disorders, effective treatments remain severely limited. Thus, the
development of novel therapeutic to treat cognitive disorders is an important goal. Here we focus on the
integrated stress response (ISR), a conserved signaling network that restores protein homeostasis by
regulating protein synthesis, and a main causative pathway underlying the memory deficits associated with a
wide range of cognitive disorders. The goal of this competing renewal is to define the precise molecular,
cellular, and circuit mechanisms by which activation of the ISR leads to cognitive dysfunction. In Aim 1, we will
generate and characterize mice carrying a human mutation in a key component of the ISR, which activates the
ISR, and is associated with intellectual disability. In Aim 2, we will generate and use state-of-the-art, novel molecular-
genetic approaches to identify the specific cell types in the brain driving the long-term memory deficits upon
activation of the ISR. Finally, in Aim 3, we will develop a novel high-throughput screening platform to identify new
inhibitors of the ISR. The results of these Aims will provide new fundamental insights into the biological basis
of cognitive dysfunction and hold the hope of opening new therapeutic avenues for cognitive disorders resulting
from perturbation of protein homeostasis.
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会议论文
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负责人:Mauro Costa-Mattioli
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依托单位:
海外基金