Abstract

Parkinson’s disease (PD) is a prevalent neurodegenerative disorder, mainly characterised by the progressive loss of dopaminergic neurons. MPP+ has been widely used as a PD-related neurotoxin, and their reports suggested the several hypotheses for neuronal cell death. However, most of these hypotheses come from the studies about the acute MPP+ exposure. We previously revealed that mild MPP+ exposure (10 and 200 μM), which induces gradual cell death, impairs autophagosome degradation at 48 h. In the present study, we further investigated the specific events of mild MPP+ exposure and revealed that mild MPP+ exposure causes the cell death through glucose starvation, but not acute toxic model (2.5 and 5 mM). At 36 h after mild MPP+ exposure, autophagosome synthesis was enhanced owing to glucose starvation and continued to enhance until 48 h, despite impaired autophagosome degradation. Inhibition of autophagosome synthesis reduced mild MPP+-induced cell death. In conclusion, we clarified that glucose starvation-enhanced autophagosome synthesis occurs at an earlier stage than impaired autophagosome degradation and is important in mild MPP+ toxicity.

Highlights

  • It is reported that MPP+ toxicity occurs simultaneously with reductions in phosphocreatine and adenosine triphosphate (ATP) as well as increases in lactic acid and glucose utilisation in different cultures, including neuroblastoma, primary neuron and rat brain slice[10,22,23,24]

  • We revealed that mild MPP+ exposure induced glucose starvation and led to cell death, whereas acute MPP+ exposure led to glucose starvation-independent cell death

  • During mild MPP+ exposure, we observed the onset of cell death with simultaneous glucose depletion (Figs 1a and 2a)

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Summary

Introduction

Mild MPP+, but not acute toxic, exposure induces glucose starvation, leading to cell death. Cell death consequent to mild MPP+ exposure was significantly reduced by glucose supplementation (Fig. 2e). Our previous report showed that mild MPP+ exposure induced the accumulation of p62/SQSTM1 (p62), a selective autophagy substrate, in a 1% Nonidet P-40 (NP-40) insoluble fraction of lysed cells[8], and we would further expect this substrate to be sequestered and aggregated in non-degraded autophagosomes.

Results
Conclusion
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