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dTOR (target of rapamycin) and dFoxo respond to changes in the nutritional environment to induce a broad range of responses in multiple tissue types. Both dTOR and dFoxo have been demonstrated to control the rate of age-related decline in cardiac function. Here, we show that the Eif4e-binding protein (d4eBP) is sufficient to protect long-term cardiac function against age-related decline and that up-regulation of dEif4e is sufficient to recapitulate the effects of high dTOR or insulin signaling. We also provide evidence that d4eBP acts tissue-autonomously and downstream of dTOR and dFoxo in the myocardium, where it enhances cardiac stress resistance and maintains normal heart rate and myogenic rhythm. Another effector of dTOR and insulin signaling, dS6K, may influence cardiac aging nonautonomously through its activity in the insulin-producing cells, possibly by regulating dilp2 expression. Thus, elevating d4eBP activity in cardiac tissue represents an effective organ-specific means for slowing or reversing cardiac functional changes brought about by normal aging.

Original publication




Journal article


Aging cell

Publication Date





542 - 552


Aging, Animals, Drosophila, Drosophila Proteins, Eukaryotic Initiation Factor-4E, Forkhead Transcription Factors, Gene Expression Regulation, Developmental, Heart, Intracellular Signaling Peptides and Proteins, Life Expectancy, Mutation, Peptide Initiation Factors, Phosphatidylinositol 3-Kinases, Protein Kinases, RNA Interference, Ribosomal Protein S6 Kinases, TOR Serine-Threonine Kinases, Vertebrates