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Intraneuronal accumulation of amyloid beta-protein (Abeta) is believed to be responsible for degeneration and apoptosis of neurons and consequent senile plaque formation in Alzheimer disease (AD), the main cause of senile dementia. Oxidative stress, an early determinant of AD, has been recently found to induce intralysosomal Abeta accumulation in cultured differentiated neuroblastoma cells through activation of macroautophagy. Because Ab is known to destabilize lysosomal membranes, potentially resulting in apoptotic cell death, this finding suggests the involvement of oxidative stress-induced macroautophagy in the pathogenesis of AD.Addendum to: Autophagy of Amyloid Beta-Protein in Differentiated Neuroblastoma Cells Exposed to Oxidative StressL. Zheng, K. Roberg, F. Jerhammar, J. Marcusson and A. TermanNeurosci Lett 2006; In press
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Zheng et al. (2006) studied this question.
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