The Brain Bank Core Resource will provide complete brain banking and neuropathology diagnostic services for all participants within the AHERF Institute on Aging. Autopsied brain material will be collected under the direction of a board-certified neuropathologist from hospitals located on the Pittsburgh and Philadelphia campuses of the Medical College of Pennsylvania/Hahnemann University. The brain will be bisected sagitally at the time of autopsy. The right half will be dissected for flash-frozen banking and distribution to participating investigators. The left half of the brain will be fixed in buffered formalin. Sections from the cerebral cortex and white matter, hippocampus, basal ganglia, cerebellum, brain stem, and spinal cord will be embedded in paraffin for microscopic examination. Paraffin sections will be routinely stained with hematoxylin and eosin. Special stains may include the Luxol fast blue periodic acid Schiff stain, the Bielschowsky silver stain, a trichrome stain, and a number of immunocytochemical stains (e.g., GFAP, beta A4, PHF). In addition to the differential diagnostics for neurodegenerative diseases, those brains found to possess changes of Alzheimer's disease will be staged according to published criteria of tangle densities. The brain bank will be catalogued and correlated with neuropathology diagnoses to make available well characterized tissues to participating AHERF investigators. Neuropathology diagnoses will be supplied to an AHERF Institute on Aging database. Based upon the analysis of autopsy reports from the past 2 years we can anticipate approximately 80 brains per year from adults with medical and surgical illnesses and no history of dementia or other complicating neurologic disease. Of those 80 brains per year approximately one-half will most likely be autopsied within 12 hours of death. Importantly, our retrospective analyses indicate that we should expect brains from adults ranging in age from more than 20-100 years of age. The availability of brain material from patients representing each decade of life provides a valuable resource to address aged-related questions. With the initiation of the Brain Bank Core Resource these control brains, as well as those with the diagnosis of Alzheimer's disease, will be banked and characterized by routine gross and microscopic neuropathologic examination. In addition, the core will maintain a reference laboratory for development of detailed and quantitative analyses.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Center Core Grants (P30)
Project #
7P30AG013282-05
Application #
6201036
Study Section
Project Start
1999-09-01
Project End
2002-06-30
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
5
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Lankenau Institute for Medical Research
Department
Type
DUNS #
125797084
City
Wynnewood
State
PA
Country
United States
Zip Code
19096
Ray, Donna; Wu, Ailing; Wilkinson, J Erby et al. (2006) Aging in heterozygous Dnmt1-deficient mice: effects on survival, the DNA methylation genes, and the development of amyloidosis. J Gerontol A Biol Sci Med Sci 61:115-24
Mo, RuRan; Chen, Jun; Grolleau-Julius, Annabelle et al. (2005) Estrogen regulates CCR gene expression and function in T lymphocytes. J Immunol 174:6023-9
Mo, Ruran; Chen, Jun; Han, Yin et al. (2003) T cell chemokine receptor expression in aging. J Immunol 170:895-904
Chen, Jun; Mo, Ruran; Lescure, Pascal A et al. (2003) Aging is associated with increased T-cell chemokine expression in C57BL/6 mice. J Gerontol A Biol Sci Med Sci 58:975-83
Lorenzini, Antonello; Tresini, Maria; Mawal-Dewan, Madhu et al. (2002) Role of the Raf/MEK/ERK and the PI3K/Akt(PKB) pathways in fibroblast senescence. Exp Gerontol 37:1149-56
Lorenzini, A; Hrelia, S; Bordoni, A et al. (2001) Is increased arachidonic acid release a cause or a consequence of replicative senescence? Exp Gerontol 36:65-78
Yung, R; Ray, D; Eisenbraun, J K et al. (2001) Unexpected effects of a heterozygous dnmt1 null mutation on age-dependent DNA hypomethylation and autoimmunity. J Gerontol A Biol Sci Med Sci 56:B268-76
Tresini, M; Lorenzini, A; Frisoni, L et al. (2001) Lack of Elk-1 phosphorylation and dysregulation of the extracellular regulated kinase signaling pathway in senescent human fibroblast. Exp Cell Res 269:287-300
Severino, J; Allen, R G; Balin, S et al. (2000) Is beta-galactosidase staining a marker of senescence in vitro and in vivo? Exp Cell Res 257:162-71
Li, M; Walter, R; Torres, C et al. (2000) Impaired signal transduction in mitogen activated rat splenic lymphocytes during aging. Mech Ageing Dev 113:85-99

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