Latrepirdine (Dimebon (TM)) Enhances Autophagy and Reduces Intracellular GFP-A beta(42) Levels in Yeast

Document Type

Journal Article

Publisher

IOS Press

Faculty

Faculty of Health, Engineering and Science

School

School of Medical Sciences / Centre of Excellence for Alzheimer's Disease Research and Care

RAS ID

15350

Grant Number

NHMRC Number : 1009295

Comments

Bharadwaj, P. R., Verdile, G., Barr, R. K., Gupta, V., Steele, J. W., Lachenmayer, M. L., ... Martins, R. N. (2012). Latrepirdine (Dimebon (TM)) Enhances Autophagy and Reduces Intracellular GFP-A beta(42) Levels in Yeast. Journal of Alzheimers Disease, 32(4), 949-967. Available here

Abstract

Latrepirdine (Dimebon (TM)), an anti-histamine, has shown some benefits in trials of neurodegenerative diseases characterized by accumulation of aggregated or misfolded protein such as Alzheimer's disease (AD) and has been shown to promote the removal of alpha-synuclein protein aggregates in vivo. An important pathway for removal of aggregated or misfolded proteins is the autophagy-lysosomal pathway, which has been implicated in AD pathogenesis, and enhancing this pathway has been shown to have therapeutic potential in AD and other proteinopathies. Here we use a yeast model, Saccharomyces cerevisiae, to investigate whether latrepirdine can enhance autophagy and reduce levels of amyloid-beta (A beta)(42) aggregates. Latrepirdine was shown to upregulate yeast vacuolar (lysosomal) activity and promote transport of the autophagic marker (Atg8) to the vacuole. Using an in vitro green fluorescent protein (GFP) tagged A beta yeast expression system, we investigated whether latrepirdine-enhanced autophagy was associated with a reduction in levels of intracellular GFP-A beta(42). GFP-A beta(42) was localized into punctate patterns compared to the diffuse cytosolic pattern of GFP and the GFP-A beta(42) (19 : 34), which does not aggregate. In the autophagy deficient mutant (Atg8 Delta), GFP-A beta(42) showed a more diffuse cytosolic localization, reflecting the inability of this mutant to sequester GFP-A beta(42). Similar to rapamycin, we observed that latrepirdine significantly reduced GFP-A beta(42) in wild-type compared to the Atg8 Delta mutant. Further, latrepirdine treatment attenuated A beta(42)-induced toxicity in wild-type cells but not in the Atg8 Delta mutant. Together, our findings provide evidence for a novel mechanism of action for latrepirdine in inducing autophagy and reducing intracellular levels of GFP-A beta(42).

DOI

10.3233/jad-2012-120178

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