Journal
APOPTOSIS
Volume 17, Issue 1, Pages 37-47Publisher
SPRINGER
DOI: 10.1007/s10495-011-0656-3
Keywords
RNA; RT-PCR arrays; Programmed cell death; Caspases; Neuroprotection; Cell culture
Categories
Funding
- Canadian Institutes of Health Research [MOP 93601]
- Canada Research Chairs program
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Deposition of amyloid-beta (A beta) protein, a 39-43 amino acid peptide, in the brain is a major pathological feature of Alzheimer's disease (AD). We have previously provided evidence that in primary cultures of rat basal forebrain and human fetal neurons (HFNs), neurotoxic effects of oligomeric A beta are expressed through the amylin receptor. In this study, we utilized RT-PCR arrays to compare RNA expression levels of 84 markers for pro and anti-apoptotic signalling pathways following exposure of HFNs to either A beta(1-42) (20 mu M) or human amylin (2 mu M). Oligomeric A beta(1-42) or human amylin was applied to HFNs alone or after pre-treatment of cultures with the amylin receptor antagonist, AC253. Changes in RNA levels were then quantified and compared to each other in order to identify increases or decreases in gene expression of apoptotic markers. Applications of A beta(1-42) or human amylin, but not the inactive inverse sequence A beta(42-1) or rat amylin, resulted in a time-dependent marked increase in mediators of apoptosis including a 10- to 30-fold elevations in caspases 3, 6, 9, BID and XIAP levels. Amylin receptor antagonists, AC253 (10 mu M) or AC187 (10 mu M), significantly attenuated the induction of several pro-apoptotic mediators up-regulated following exposure to A beta(1-42) or human amylin and increased the expression of several antiapoptotic markers. These data allow us to identify key elements in the A beta-induced apoptosis that are blocked by antagonism of the amylin receptor and further support the potential for amylin receptor blockade as a potential therapeutic avenue in AD.
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