TY - JOUR
T1 - Phosphatidylethanolamine positively regulates autophagy and longevity
AU - Rockenfeller, P.
AU - Koska, M.
AU - Pietrocola, F.
AU - Minois, N.
AU - Knittelfelder, O.
AU - Sica, V.
AU - Franz, J.
AU - Carmona-Gutierrez, D.
AU - Kroemer, G.
AU - Madeo, F.
N1 - Publisher Copyright:
© 2015 Macmillan Publishers Limited All rights reserved.
PY - 2015/1/1
Y1 - 2015/1/1
N2 - Autophagy is a cellular recycling program that retards ageing by efficiently eliminating damaged and potentially harmful organelles and intracellular protein aggregates. Here, we show that the abundance of phosphatidylethanolamine (PE) positively regulates autophagy. Reduction of intracellular PE levels by knocking out either of the two yeast phosphatidylserine decarboxylases (PSD) accelerated chronological ageing-associated production of reactive oxygen species and death. Conversely, the artificial increase of intracellular PE levels, by provision of its precursor ethanolamine or by overexpression of the PE-generating enzyme Psd1, significantly increased autophagic flux, both in yeast and in mammalian cell culture. Importantly administration of ethanolamine was sufficient to extend the lifespan of yeast (Saccharomyces cerevisiae), mammalian cells (U2OS, H4) and flies (Drosophila melanogaster). We thus postulate that the availability of PE may constitute a bottleneck for functional autophagy and that organismal life or healthspan could be positively influenced by the consumption of ethanolamine-rich food.
AB - Autophagy is a cellular recycling program that retards ageing by efficiently eliminating damaged and potentially harmful organelles and intracellular protein aggregates. Here, we show that the abundance of phosphatidylethanolamine (PE) positively regulates autophagy. Reduction of intracellular PE levels by knocking out either of the two yeast phosphatidylserine decarboxylases (PSD) accelerated chronological ageing-associated production of reactive oxygen species and death. Conversely, the artificial increase of intracellular PE levels, by provision of its precursor ethanolamine or by overexpression of the PE-generating enzyme Psd1, significantly increased autophagic flux, both in yeast and in mammalian cell culture. Importantly administration of ethanolamine was sufficient to extend the lifespan of yeast (Saccharomyces cerevisiae), mammalian cells (U2OS, H4) and flies (Drosophila melanogaster). We thus postulate that the availability of PE may constitute a bottleneck for functional autophagy and that organismal life or healthspan could be positively influenced by the consumption of ethanolamine-rich food.
UR - http://www.scopus.com/inward/record.url?scp=84922576844&partnerID=8YFLogxK
U2 - 10.1038/cdd.2014.219
DO - 10.1038/cdd.2014.219
M3 - Article
C2 - 25571976
AN - SCOPUS:84922576844
SN - 1350-9047
VL - 22
SP - 499
EP - 508
JO - Cell Death and Differentiation
JF - Cell Death and Differentiation
IS - 3
ER -