Neurotoxicity Research

, Volume 22, Issue 3, pp 208–219

Amyloid-β Production: Major Link Between Oxidative Stress and BACE1

Review Article

DOI: 10.1007/s12640-011-9283-6

Cite this article as:
Tamagno, E., Guglielmotto, M., Monteleone, D. et al. Neurotox Res (2012) 22: 208. doi:10.1007/s12640-011-9283-6


Sequential endoproteolytic cleavages operated by the γ-secretase and the β-secretase (BACE1) on the β-amyloid precursor protein result in the production of the β-amyloid (Aβ) species, with two C-terminal variants, at residue 40 or at residue 42. Accumulation in brain tissue of aggregates of Aβ42 is the major pathogenetic event in Alzheimer’s disease (AD). The causes of Aβ accumulation in the common sporadic form of AD are not completely understood, but they are likely to include oxidative stress (OS). Data reviewed here shed light on how Aβ generation, oxidative stress, and secretase functions are intimately related in sporadic AD. According to our hypothesis, in sporadic AD, OS resulted from several cellular insults such as aging, hypoxia, hyperglycemia, and hypercholesterolemia—that are well-known risk factors for AD development—can determine a primary induction of γ-secretase and BACE1. The loop proceeds with the generation of Aβ42 and its signaling to BACE1 transcription.


Alzheimer’s disease BACE1 Oxidative stress β-amyloid 

Copyright information

© Springer Science+Business Media, LLC 2011

Authors and Affiliations

  1. 1.General Pathology Section, Department of Experimental Medicine and OncologyUniversity of TorinoTurinItaly
  2. 2.Neuroscience Institute of the Cavalieri Ottolenghi Foundation (NICO)University of TorinoTurinItaly
  3. 3.Unit of Geriatric Medicine, Department of Internal MedicineUniversity of GenovaGenoaItaly

Personalised recommendations