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Published on: August 15, 2025
The longevity effects of reduced IGF-1 signaling depend on the stability of the mitochondrial genome
Sarah J Shemtov1, Eric McGann1, Lucy Carrillo1
1Leonard Davis School of Gerontology, University of Southern California, Los Angeles, CA, USA.
Abstract:
Suppression of insulin-like growth factor-1 (IGF-1) signaling extends mammalian life span and protects against a range of age-related diseases. Unexpectedly, we found that reduced IGF-1 signaling fails to extend the life span of mitochondrial mutator mice. Most of the longevity pathways that are normally initiated by IGF-1 suppression were either blocked or blunted in the mutator mice. These observations suggest that the prolongevity effects of IGF-1 suppression critically depend on the integrity of the mitochondrial genome, revealing an unexpected hierarchy in the pathways that control mammalian aging. Together, these findings deepen our understanding of the interactions between the hallmarks of aging and underscore the need for interventions that preserve the integrity of the mitochondrial genome.
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