Abstract
Alzheimer's disease is a neurodegenerative disorder characterised by extracellular accumulation of the Abeta peptide, derived from the amyloid precursor protein (APP). The function of APP as a cell surface receptor was examined by ligand-mimicking using an antibody against the APP extracellular domain. Alterations in gene expression evoked by antibody-bound APP were analysed using human pathway-finder gene arrays and the largest change in expression levels was found for ornithine decarboxylase (ODC). These results were confirmed by Western blotting which showed even higher upregulation on the protein level. APP knockdown by RNAi verified that upregulation of ODC was APP-mediated. This APP signalling event did not require gamma-secretase cleavage, as it was independent of the presence of presenilin-1 or -2. The induced ODC expression was rapid and biphasic, resembling growth-factor stimulated signalling events. This study shows that antibody-bound APP leads to altered gene expression that may be relevant to AD.
| Original language | English |
|---|---|
| Journal | Biochemical and Biophysical Research Communications |
| Volume | 341 |
| Issue number | 4 |
| Pages (from-to) | 1294-9 |
| Number of pages | 6 |
| ISSN | 0006-291X |
| DOIs | |
| Publication status | Published - 24 Mar 2006 |
| Externally published | Yes |
Keywords
- Amyloid beta-Protein Precursor
- Antigen-Antibody Complex
- Cells, Cultured
- Gene Expression Regulation, Enzymologic
- Humans
- Journal Article
- Membrane Proteins
- Ornithine Decarboxylase
- Presenilin-1
- Presenilin-2
- Research Support, Non-U.S. Gov't
- Tumor Cells, Cultured
- Up-Regulation
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