Journal
NEUROSCIENCE
Volume 120, Issue 3, Pages 659-665Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0306-4522(03)00342-7
Keywords
Trk B; beta-amyloid; melatonin; Alzheimer's disease; oxidative stress; SHSY5Y neuroblastoma cells
Categories
Ask authors/readers for more resources
Alzheimer's disease (AD) is the most prevalent neurodegenerative disease in humans and is characterized by neuronal loss, neurofibrillary tangles and P-amyloid deposition. The interaction between neurotrophins and their tyrosine kinase (trk) receptors is important for cellular differentiation and survival. Interestingly, marked reductions in neurotrophins and receptors have been reported in AD. The cause of the decrease in these molecules remains unclear. However, the role of beta-amyloid (AP) appears central in understanding the mechanisms controlling neurotrophin/trk expression. In this study we exposed SHSY5Y neuroblastoma cells to AP or hydrogen peroxide and measured the expression of trk B/truncated trk B, and brain-derived neurotrophic factor (BDNF)/NT4 at the protein and molecular level. We show that Abeta or hydrogen peroxide (H2O2) induces oxidative stress and cell cytotoxicity. The exposure of cells to AP results in an increased trk B expression with a concurrent reduction in truncated trk B levels. H2O2 exposure decreased both trk B and truncated trk B levels at the cell surface. At the molecular level trk B RNA increased in the presence of AP and was unaffected by H2O2. Similarly, BDNF and NT4 levels increased in the presence of Abeta. Pre-treatment of cells with the anti-oxidant mellatonin returns trk receptor expression, mRNA and BDNF/NT4 secretion to normal levels. These results are significant as they can help in the planning and implementation of AD treatment strategies involving neurotrophins. (C) 2003 IBRO. Published by Elsevier Science Ltd. All rights reserved.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available