Astrocytes contribute to neuronal impairment in beta A toxicity increasing apoptosis in rat hippocampal neurons

Glia. 2001 Apr 1;34(1):68-72. doi: 10.1002/glia.1041.

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alzheimer Disease / physiopathology
  • Amyloid beta-Peptides / pharmacology*
  • Animals
  • Apoptosis / drug effects*
  • Apoptosis / physiology
  • Astrocytes / drug effects*
  • Astrocytes / physiology
  • Cells, Cultured
  • Cerebral Cortex
  • Embryo, Mammalian
  • Hippocampus / drug effects*
  • Hippocampus / physiology
  • Neurons / drug effects*
  • Neurons / physiology
  • Rats
  • Rats, Wistar

Substances

  • Amyloid beta-Peptides