This continuation application is to provide advanced training to predoctoral and postdoctoral fellows in the fundamentals of neuronal plasticity in the aging nervous system. The program has three key features: 1) Academic bridging - A principal focus will be to provide the students and fellows with concepts and research experience that address problems at the interface of basic and clinical problems in aging. This bridging will be reflected in the faculty participating in the program, the trainees admitted to the program, and the structure of the training program itself. Courses, seminars, annual scientific retreat, and co-sponsorships by basic scientists and clinical researchers of trainees will bring together these bridging concepts and research practice. 2) Life span development - We believe that the aging process is part of a life span process, which should and can be investigated as part of a continuum from birth to death. Many conceptual and practical problems presently being addressed in early development are translatable to late stage aging. This translation of ideas and approaches from studies of development and adult plasticity will be a feature of the program. We believe that investigations of neuronal plasticity are at the very core of understanding late stage aging of the nervous system, since age-related decline often reflects a decrease in neuronal and functional plasticity. In this program, we will encourage the participants to address these age-related aspects of plasticity, disease, and neurodegeneration. 3) Multi-disciplinary - By its very nature, Neuroscience and Aging are multi-disciplinary fields of investigation. The modern neuroscientist is required to understand and use methods and techniques from the full range of biological disciplines and beyond. The faculty in this program (46 at current time) represents technical expertise in the fields of Molecular Genetics, Protein Chemistry, Cell Biology, Neurophysiology, Systems Analysis, Pharmacology, Cognitive Neuroscience, Computational Neuroscience, and Clinical Neurology. The students (six per year at second year of training and beyond) are drawn from the Neurosciences Graduate Program, a highly regarded program with strong participation from UCSD and the neighboring institutions, including Salk, Scripps, and Sanford-Burnham Institutes. Postdoctoral trainees (six per year) are drawn from the laboratories of the same participating faculty members. Our goal is to train students and fellows to be able to work and think effectively in several of these areas and will be achieved by providing them a forum for instruction, discussion, and interaction; in so doing, they represent the next generation of neuroscientists who will contribute to the advancement in aging research.

Public Health Relevance

This continuation application for five years support is to provide advanced training to predoctoral and postdoctoral fellows in studying neurobiology of the aging nervous system. The aging of the US population means a continued need for new investigators trained in the study of the aged nervous system. This Training Program hopes to use a multi-disciplinary approach through courses, seminars, talks, and advisory groups to prepare the trainees for a career in neurobiological research focused on neurobiology of aging and age-associated neurological diseases.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Institutional National Research Service Award (T32)
Project #
5T32AG000216-24
Application #
8842905
Study Section
Special Emphasis Panel (ZAG1-ZIJ-3 (J1))
Program Officer
Wise, Bradley C
Project Start
1992-09-30
Project End
2017-04-30
Budget Start
2015-05-01
Budget End
2016-04-30
Support Year
24
Fiscal Year
2015
Total Cost
$643,958
Indirect Cost
$42,306
Name
University of California San Diego
Department
Neurosciences
Type
Schools of Medicine
DUNS #
804355790
City
La Jolla
State
CA
Country
United States
Zip Code
92093
Hsu, Cynthia L; Lee, Elian X; Gordon, Kara L et al. (2018) MAP4K3 mediates amino acid-dependent regulation of autophagy via phosphorylation of TFEB. Nat Commun 9:942
Lake, Blue B; Chen, Song; Sos, Brandon C et al. (2018) Integrative single-cell analysis of transcriptional and epigenetic states in the human adult brain. Nat Biotechnol 36:70-80
Urgolites, Zhisen J; Smith, Christine N; Squire, Larry R (2018) Eye movements support the link between conscious memory and medial temporal lobe function. Proc Natl Acad Sci U S A 115:7599-7604
Lee, Ming-Hsiang; Siddoway, Benjamin; Kaeser, Gwendolyn E et al. (2018) Somatic APP gene recombination in Alzheimer's disease and normal neurons. Nature 563:639-645
Devarajan, Priyadharshini; Jones, Michael C; Kugler-Umana, Olivia et al. (2018) Pathogen Recognition by CD4 Effectors Drives Key Effector and Most Memory Cell Generation Against Respiratory Virus. Front Immunol 9:596
Meves, Jessica M; Geoffroy, Cédric G; Kim, Noah D et al. (2018) Oligodendrocytic but not neuronal Nogo restricts corticospinal axon sprouting after CNS injury. Exp Neurol 309:32-43
Daugherty, Daniel J; Marquez, Alexandra; Calcutt, Nigel A et al. (2018) A novel curcumin derivative for the treatment of diabetic neuropathy. Neuropharmacology 129:26-35
Cheng, Weiwei; Wang, Shaopeng; Mestre, Alexander A et al. (2018) C9ORF72 GGGGCC repeat-associated non-AUG translation is upregulated by stress through eIF2? phosphorylation. Nat Commun 9:51
Geoffroy, Cédric G; Meves, Jessica M; Zheng, Binhai (2017) The age factor in axonal repair after spinal cord injury: A focus on neuron-intrinsic mechanisms. Neurosci Lett 652:41-49
Urgolites, Zhisen J; Hopkins, Ramona O; Squire, Larry R (2017) Medial temporal lobe and topographical memory. Proc Natl Acad Sci U S A 114:8626-8630

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