Induction of autophagy by spermidine promotes longevity

Abstract

Ageing results from complex genetically and epigenetically programmed processes that are elicited in part by noxious or stressful events that cause programmed cell death. Here, we report that administration of spermidine, a natural polyamine whose intracellular concentration declines during human ageing, markedly extended the lifespan of yeast, flies and worms, and human immune cells. In addition, spermidine administration potently inhibited oxidative stress in ageing mice. In ageing yeast, spermidine treatment triggered epigenetic deacetylation of histone H3 through inhibition of histone acetyltransferases (HAT), suppressing oxidative stress and necrosis. Conversely, depletion of endogenous polyamines led to hyperacetylation, generation of reactive oxygen species, early necrotic death and decreased lifespan. The altered acetylation status of the chromatin led to significant upregulation of various autophagy-related transcripts, triggering autophagy in yeast, flies, worms and human cells. Finally, we found that enhanced autophagy is crucial for polyamine-induced suppression of necrosis and enhanced longevity.

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Affiliated Institutions

• Research Institute of Molecular Pathology AT
• University of Graz AT
• Gladstone Institutes US
• Inserm FR
• University of Basel CH
• Foundation for Research and Technology Hellas GR
• Institute of Molecular Biotechnology AT
• BOKU University AT
• Austrian Academy of Sciences AT
• Joanneum Research AT
• Institut Gustave Roussy FR
• University of Salzburg AT

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