CREB-binding protein levels in the rat hippocampus fail to predict chronological or cognitive aging
Autor: | Michela Gallagher, Christopher E. Coletta, Evelyn V. Perez, Peter R. Rapp, Inês Tomás Pereira, Ilya G. Goldberg, David H. Kim |
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Rok vydání: | 2013 |
Předmět: |
Male
Aging Morris water navigation task Hippocampal formation Hippocampus Article Epigenesis Genetic Histones Cognition Gene expression Animals Rats Long-Evans CREB-binding protein Maze Learning Histone Acetyltransferases Memory Disorders biology General Neuroscience Acetylation Histone acetyltransferase CREB-Binding Protein Rats Histone biology.protein Neurology (clinical) Geriatrics and Gerontology Neuroscience Biomarkers Immunostaining Developmental Biology |
Zdroj: | Neurobiology of Aging. 34:832-844 |
ISSN: | 0197-4580 |
DOI: | 10.1016/j.neurobiolaging.2012.07.010 |
Popis: | Normal cognitive aging is associated with deficits in memory processes dependent on the hippocampus, along with large-scale changes in the hippocampal expression of many genes. Histone acetylation can broadly influence gene expression and has been recently linked to learning and memory. We hypothesized that cAMP response element binding (CREB)-binding protein (CBP), a key histone acetyltransferase, may contribute to memory decline in normal aging. Here, we quantified CBP protein levels in the hippocampus of young, aged unimpaired and aged impaired rats, classified on the basis of spatial memory capacity documented in the Morris water maze. First, CBP-immunofluorescence was quantified across the principal cell layers of the hippocampus using both low and high resolution laser scanning imaging approaches. Second, digital images of CBP immunostaining were analyzed by a multi-purpose classifier algorithm (WND-CHARM) with validated sensitivity across many types of input materials. Finally, CBP protein levels in the principal subfields of the hippocampus were quantified by quantitative western blotting. CBP levels were equivalent as a function of age and cognitive status in all analyses. The sensitivity of the techniques used was substantial, sufficient to reveal differences across the principal cell fields of the hippocampus, and to correctly classify images from young and aged animals independent of CBP-immunoreactivity. The results are discussed in the context of recent evidence suggesting that CBP decreases may be most relevant in conditions of aging that, unlike normal cognitive aging, involve significant neuron loss. |
Databáze: | OpenAIRE |
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