## Abstract The β‐amyloid protein (Aβ) is derived by proteolytic processing of the amyloid protein precursor (APP). Cleavage of APP by β‐secretase generates a C‐terminal fragment (APP‐CTFβ), which is subsequently cleaved by γ‐secretase to produce Aβ. Our previous studies have shown that the proteas
Effect of cell density on intracellular levels of the Alzheimer's amyloid precursor protein
✍ Scribed by Sandra Rebelo; Ana Gabriela Henriques; Edgar F. da Cruz e Silva; Odete A.B. da Cruz e Silva
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 328 KB
- Volume
- 76
- Category
- Article
- ISSN
- 0360-4012
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✦ Synopsis
Abstract
The precise function of APP (Alzheimer's amyloid precursor protein) remains to be fully elucidated, but various lines of evidence suggest that it may be involved in cell adhesion processes. Because APP is a transmembrane glycoprotein, variations in its expression level may have direct bearing on its putative role in cell adhesion. Our results revealed that although APP levels did not change markedly with increasing cell density (ICD), there was a small but reproducible increase in APP expression at subconfluent conditions. Higher expression APP levels led to corresponding increases in the amount of APP processed and secreted APP (sAPP) released into the cell media. Given that phorbol esters stimulate the non‐amyloidogenic pathway at the expense of reducing production of Aβ (the peptide found deposited as neuritic plaques in the brains of patients with Alzheimer's disease), thus providing an interesting therapeutic focus, we tested the effect of the phorbol 12‐myristate 13‐acetate (PMA) on APP processing at ICD. PMA not only stimulated sAPP release at all densities tested, but also produced a corresponding decrease in the intracellular levels of APP. Further experimentation revealed that increased APP expression with ICD was dependent on factors present in conditioned medium. Interestingly, exposing cells to the Aβ peptide itself could mimic these results, thus providing evidence for a potential positive feedback mechanism between Aβ production and intracellular APP levels. © 2004 Wiley‐Liss, Inc.
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The main component of the amyloid plaques found in the brains of those with Alzheimer's disease (AD) is a polymerized form of the b-amyloid peptide (Ab) and is considered to play a central role in the pathogenesis of this neurodegenerative disorder. Ab is derived from the proteolytic processing of t
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