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Spermidine is essential for fasting-mediated autophagy and longevity

Hofer SJ, Daskalaki I, Bergmann M, Friščić J, Zimmermann A, Mueller MI, Abdellatif M, Eisenberg T, Tavernarakis N, Kroemer G, Madeo F · 2024 · Nature Cell Biology

DOI: 10.1038/s41556-024-01468-xView source ↗

Genetic or pharmacological blockade of spermidine synthesis reduces fasting-induced autophagy in yeast, nematodes, and human cells.

Summary

This 2024 Nature Cell Biology paper from the Madeo lab identified spermidine — a polyamine found in many foods (wheat germ, soybeans, mushrooms, aged cheeses) and produced endogenously — as the essential mediator of fasting-induced autophagy. The authors ran experiments across multiple model systems: yeast, nematodes, mouse cells, and human cell lines (U2OS osteosarcoma cells and H4 neuroglioma cells). Across all systems, blocking spermidine synthesis with the inhibitor DFMO suppressed fasting-induced autophagy — and supplementing exogenous spermidine (100 µM) rescued the autophagy response. The paper also reports human-cohort metabolomics: across multiple cohorts of fasting participants (61 to 109 volunteers per cohort, fasting durations 3 to 16 days), serum spermidine levels rose during fasting. Human PBMCs showed increased hypusination of eIF5A — a downstream effect linking spermidine to translation control and autophagy machinery. The paper's mechanistic claim is significant: spermidine is not just correlated with fasting-induced autophagy; it is required for the response to occur.

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