This program consists of collaborative projects on molecular aspects of the normal and pathological brain aging, focused on neuronal fibrous protein structures: neurofilaments and microtubules. Particular attention will be given to molecular abnormalities seen in Alzheimer disease post mortem brain tissue. Extensive analyses will be carried out on the hallmark neuronal lesion of this disease entity, the paired helical filament. Four interrelated projects are proposed: (1) The molecular structure and subcellular distribution of human, mouse and rabbit neurofilament and microtubule proteins; studies on normal age-related alterations in mammalian CNS fibrous proteins; the normal aging of the synaptic architecture. (II) Macromolecular changes in human and animal brain aging at the level of messsenger RNA, protein synthesis and post-translational modification. (III) Alterations of neurofilament subunits and mRNA translation products in an experimental (aluminum) model of fialmentous degeneration of neurons. (IV) Macromolecular alterations affecting neurofilament subunits in human neuronal aging and in dementia of the Alzheimer type. This Program will be carried out as a collaborative effort by Neurochemistry and Neuropathology Laboratories of the Mailman Research Center, McLean Hospital, a division of the Massachusetts General Hospital and affiliated with the Harvard Medical School.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Program Projects (P01)
Project #
3P01AG002126-08S1
Application #
3090597
Study Section
Aging Review Committee (AGE)
Project Start
1980-04-01
Project End
1988-11-30
Budget Start
1988-09-01
Budget End
1988-11-30
Support Year
8
Fiscal Year
1988
Total Cost
Indirect Cost
Name
Mc Lean Hospital (Belmont, MA)
Department
Type
DUNS #
City
Belmont
State
MA
Country
United States
Zip Code
02478
Li, J; Hertzberg, E L; Nagy, J I (1997) Connexin32 in oligodendrocytes and association with myelinated fibers in mouse and rat brain. J Comp Neurol 379:571-91
Nagy, J I; Hossain, M Z; Hertzberg, E L et al. (1996) Induction of connexin43 and gap junctional communication in PC12 cells overexpressing the carboxy terminal region of amyloid precursor protein. J Neurosci Res 44:124-32
Sandhu, F A; Kim, Y; Lapan, K A et al. (1996) Expression of the C terminus of the amyloid precursor protein alters growth factor responsiveness in stably transfected PC12 cells. Proc Natl Acad Sci U S A 93:2180-5
Nagy, J I; Li, W; Hertzberg, E L et al. (1996) Elevated connexin43 immunoreactivity at sites of amyloid plaques in Alzheimer's disease. Brain Res 717:173-8
Lynn, B D; Marotta, C A; Nagy, J I (1995) Propagation of intercellular calcium waves in PC12 cells overexpressing a carboxy-terminal fragment of amyloid precursor protein. Neurosci Lett 199:21-4
Friedland, R P; Majocha, R E; Reno, J M et al. (1994) Development of an anti-A beta monoclonal antibody for in vivo imaging of amyloid angiopathy in Alzheimer's disease. Mol Neurobiol 9:107-13
Maestre, G E; Tate, B A; Majocha, R E et al. (1994) Intercellular interactions in PC12 cells overexpressing beta/A4 amyloid. Scanning Microsc 8:325-35;discussion 335-6
Majocha, R E; Agrawal, S; Tang, J Y et al. (1994) Modulation of the PC12 cell response to nerve growth factor by antisense oligonucleotide to amyloid precursor protein. Cell Mol Neurobiol 14:425-37
Leli, U; Shea, T B; Cataldo, A et al. (1993) Differential expression and subcellular localization of protein kinase C alpha, beta, gamma, delta, and epsilon isoforms in SH-SY5Y neuroblastoma cells: modifications during differentiation. J Neurochem 60:289-98
Majocha, R E; Tate, B; Marotta, C A (1993) PC12 cells release stimulatory factors after transfection with beta/A4-C-terminal DNA of the Alzheimer amyloid precursor protein. Mol Chem Neuropathol 18:99-113

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