Generation, Characterization, and Validation of Marmoset Models of Alzheimer's Disease - Project Summary…
FY2022 · complete year · data as of 2026-07-11
A single federal award, with both ends of the trail linked.
Award U19AG074866 is a grant from the Department of Health and Human Services to University of Pittsburgh - of the Commonwealth System of Higher Education, $36.7M obligated, FY2022 to FY2027, for Generation, Characterization, and Validation of Marmoset Models of Alzheimer's Disease - Project…. The work is performed in Pennsylvania. Source
Description
Generation, Characterization, and Validation of Marmoset Models of Alzheimer's Disease - Project Summary Overall Alzheimer’s Disease (Ad) Is a Devastating Neurodegenerative Disorder Affecting Nearly 6 Million Americans and Is Expected to Increase Over the Next Several Years. Our Limited Understanding of the Mechanisms That Trigger the Emergence of Ad Has Contributed to the Lack of Interventions That Stop, Prevent, or Fully Treat This Disease. We Propose to Establish the Marmoset as the First Primate-Specific Model to Reveal the Earliest Cellular and Molecular Events of Ad Processes and Allow Charting Ad Progression from Its Inception. To Do So, We Will Draw from a Self-Sufficient and Large Colony of Research Marmosets with Dedicated Veterinary and Husbandry Teams, State-Of-The-Art in Vivo Neuroimaging and Molecular Assays, and a Multidisciplinary Team of Experts in Aging Biology, Ad Genetics and Genomics, Animal Model Development and Characterization, Behavioral and Cognitive Phenotyping, and Marmoset Gene-Editing Technologies. Our Proposal’s Overarching Goals Are to Develop Marmoset Models of Early-Onset Ad (Eoad) and Late-Onset Ad (Load) to Enable the Investigation of the Underlying Cellular and Molecular Root Causes of the Pathogenesis and Progression of Ad and Support Future Translational Studies. We Believe That the Simultaneous Assessment of Genetic, Molecular, Functional, Behavioral, and Pathological Phenotypes in Marmosets Will Provide Translatable Knowledge of the Origins and Progression of Ad in Human Populations. Furthermore, We Posit That the Comprehensive Study of Gene-Edited Marmoset Models of Ad from Neurodevelopment Through Aging Will Identify Emerging Phenotypes That Precede Frank Neuropathology. Our Proposal Consists of 3 Integrated Research Projects That Aim to: (1) Conduct Characterization and Validation of PSEN1 Mutations in Marmosets as a Model for the Study of Eoad, and Investigate Early Life Molecular Determinants of Ad Disease Pathogenesis Associated with Genetic Risk for Eoad; (2) Identify and Enhance Load-Related Signatures in Outbred and Genetically-Engineered Marmosets; and (3) Conduct a Comparative Multimodal Phenotypic Characterization of Marmoset Models of Ad. These Projects Will Be Supported by 5 Research Cores Focused on Project Administration, Bioinformatics, Genetic Engineering, Multimodal Disease Characterization, and Veterinary and Colony Management. These Supporting Cores Will Integrate Marmoset and Human Genomic Signatures and Provide Data Dissemination and Resources to the Greater Research Community as Part of Our Commitment to Open Science, Generate Novel Gene-Edited Marmoset Models of Ad, Develop Optimized Protocols for Studying Disease Onset and Trajectory in Line with Clinical Protocols, Evaluate Therapeutic Strategies, and Provide Specialized Animal Care and Support, Respectively, Allowing Complete Characterization of the Marmoset Models. At the Conclusion of This Project, We Will Have Genetically Engineered Three Ad Risk Variants Into Marmoset Models, Established a Disease Characterization Pipeline for Comprehensive Phenotyping, and Shared These Resources with the Greater Research Community.