Protection against an increase in pro-inflammatory factors with agePeer-Reviewed Publication
MAX PLANCK INSTITUTE FOR BIOLOGY OF AGEING
RAPAMYCIN IS ONE OF THE MOST PROMISING ANTI-AGEING SUBSTANCES TO DATE. RAPAMYCIN IS NAMED AFTER “RAPA NUI”, THE LOCAL TRANSLATION FOR THE EASTER ISLANDS, WHERE THE ACTIVE INGREDIENT WAS DISCOVERED AS A METABOLIC PRODUCT OF BACTERIA IN A SOIL SAMPLE.
CREDIT: K. LINK/ MAX PLANCK INSTITUTE FOR BIOLOGY OF AGEING
The therapeutic drug rapamycin, which is normally used in cancer therapy and after organ transplants, can extend the lifespan and health span of laboratory animals. Understanding how rapamycin extend lifespan is important, as it helps to prevent unwanted side effects. “We know that rapamycin extends lifespan via two mechanisms: increased autophagy and decreased activity of a protein called S6K. It has been shown that mice with altered S6K live longer. But the mechanism by which S6K extends lifespan is unclear,” says Sebastian Grönke, co-author of the study.
Better immune function in old age thanks to endolysosomes
The researchers were able to show that an altered activity of S6K influences the endolysosomes. These break down material in the cells and play an important role in regulating various cellular processes, such as inflammatory reactions. “When we suppressed S6K activity or the inflammatory signalling in the fat body, the flies lived longer, showed better immune function at old age and were able to clear bacterial infections more efficiently,” explains Pingze Zhang, first author of the study. “Ultimately, we assume that the endolysosomes prevent the age-related increase in pro-inflammatory factors and that this is precisely where rapamycin attacks,” concludes Sebastian Grönke.
Syntaxin 13: a link also found in mice
The researchers also identified an important link between the endolysosomal system and age-related inflammation: the protein syntaxin 13. This protein is increased in the liver of rapamycin-treated mice, suggesting that the regulation of the endolysosomal system and the control of inflammatory pathways during ageing is similar between flies and mice.
JOURNAL
Nature Aging
DOI
10.1038/s43587-024-00578-3
METHOD OF RESEARCH
Experimental study
SUBJECT OF RESEARCH
Animals
ARTICLE TITLE
Nature Aging
ARTICLE PUBLICATION DATE
27-Feb-2024
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