| Literature DB >> 11284021 |
F Malchiodi-Albedi1, M R Domenici, S Paradisi, A Bernardo, M A Ajmone-Cat, L Minghetti.
Abstract
Astrocytosis is a common feature of amyloid plaques, the hallmark of Alzheimer's disease (AD), along with activated microglia, neurofibrillary tangles, and beta-amyloid (beta A) deposition. However, the relationship between astrocytosis and neurodegeneration remains unclear. To assess whether beta A-stimulated astrocytes can damage neurons and contribute to beta A neurotoxicity, we studied the effects of beta A treatment in astrocytic/neuronal co-cultures, obtained from rat embryonic brain tissue. We found that in neuronal cultures conditioned by beta A-treated astrocytes, but not directly in contact with beta A, the number of apoptotic cells increased, doubling the values of controls. In astrocytes, beta A did not cause astrocytic cell death, nor did produce changes in nitric oxide or prostaglandin E(2) levels. In contrast, S-100 beta expression was remarkably increased. Our data show for the first time that beta A--astrocytic interaction produces a detrimental effect on neurons, which may contribute to neurodegeneration in AD. Copyright 2001 Wiley-Liss, Inc.Entities:
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Year: 2001 PMID: 11284021 DOI: 10.1002/glia.1041
Source DB: PubMed Journal: Glia ISSN: 0894-1491 Impact factor: 7.452