3.9 Article

Cell Self-Eating (Autophagy) Mechanism in Alzheimer's Disease

Journal

MOUNT SINAI JOURNAL OF MEDICINE
Volume 77, Issue 1, Pages 59-68

Publisher

WILEY
DOI: 10.1002/msj.20161

Keywords

Alzheimer's disease; amyloidogenesis; autophagy; dysfunction; endosomal-lysosomal pathway

Funding

  1. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R01NS060123] Funding Source: NIH RePORTER
  2. NINDS NIH HHS [R01 NS060123, R01 NS060123-02] Funding Source: Medline

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The autophagy pathway is the major degradation pathway of the cell for long-lived proteins and organelles. Dysfunction of autophagy has been linked to several neurodegenerative disorders that are associated with an accumulation of rnisfolded protein aggregates. Alzheimer's disease, the most common neurodegenerative disorder, is characterized by 2 aggregate forms, tau tangles and amyloid-beta plaques. Autophagy has been linked to Alzheimer's disease pathogenesis through its merger with the endosomal-lysosomal system, which has been shown to play a role in the formation of the latter amyloid-beta plaques. However, the precise role of autophagy in Alzheimer's disease pathogenesis is Still under contention. One hypothesis is that aberrant autophagy induction results in an accumulation of autophagic vacuoles containing amyloid-beta and the components necessary for its generation, whereas other evidence points to impaired autophagic clearance or even an overall reduction in autophagic activity playing a role in Alzheimer's disease pathogenesis. In this review, we discuss the Current evidence linking autophagy to Alzheimer's disease as well as the uncertainty over the exact role and level of autophagic regulation in the pathogenic mechanism of Alzheimer's disease. Mt Sinai J Med 77:59-68, 2010. (C) 2010 Mount Sinai School of Medicine

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