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Amyloid beta and the longest-lived rodent: the naked mole-rat as a model for natural protection from Alzheimer's disease
Authors:Yael H. Edrey  David X. Medina  Maria Gaczynska  Pawel A. Osmulski  Salvatore Oddo  Antonella Caccamo  Rochelle Buffenstein
Affiliation:1. Department of Physiology, University of Texas Health Science Center, San Antonio, TX, USA;2. Barshop Institute for Longevity and Aging Studies, San Antonio, TX, USA;3. Department of Molecular Medicine, Institute of Biotechnology, University of Texas Health Science Center, San Antonio, TX, USA
Abstract:Amyloid beta (Aβ) is implicated in Alzheimer's disease (AD) as an integral component of both neural toxicity and plaque formation. Brains of the longest-lived rodents, naked mole-rats (NMRs) approximately 32 years of age, had levels of Aβ similar to those of the 3xTg-AD mouse model of AD. Interestingly, there was no evidence of extracellular plaques, nor was there an age-related increase in Aβ levels in the individuals examined (2–20+ years). The NMR Aβ peptide showed greater homology to the human sequence than to the mouse sequence, differing by only 1 amino acid from the former. This subtle difference led to interspecies differences in aggregation propensity but not neurotoxicity; NMR Aβ was less prone to aggregation than human Aβ. Nevertheless, both NMR and human Aβ were equally toxic to mouse hippocampal neurons, suggesting that Aβ neurotoxicity and aggregation properties were not coupled. Understanding how NMRs acquire and tolerate high levels of Aβ with no plaque formation could provide useful insights into AD, and may elucidate protective mechanisms that delay AD progression.
Keywords:Alzheimer's disease   Amyloid beta   Naked mole-rat   Aggregation   Neuronal toxicity   3xTg-AD mice   Heterocephalus glaber
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