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Modulating mTOR in aging and health
Simon C Johnson1, Maya Sangesland, Matt Kaeberlein
1Department of Pathology, University of Washington, Seattle, Wash., USA.
Nutrient availability impacts aging and disease through cellular signaling. Reducing mechanistic target of rapamycin (mTOR) activity extends lifespan across species, offering potential therapeutic targets for human aging and disease.
Area of Science:
- Cellular and Molecular Biology
- Geroscience
- Pharmacology
Background:
- Physiological responses to nutrient availability are critical in aging and disease.
- Conserved cellular signaling pathways link nutrient/hormone cues to cellular growth and maintenance.
- The mechanistic target of rapamycin (mTOR) pathway is a key regulator of aging across diverse organisms.
Purpose of the Study:
- To highlight the central role of mTOR signaling in aging and age-related diseases.
- To emphasize the therapeutic potential of targeting mTOR for human healthspan interventions.
- To review the conserved nature of mTOR in modulating aging from yeast to mammals.
Main Methods:
- Review of genetic and pharmacological studies on nutrient-sensing pathways.
- Analysis of conserved cellular signaling mechanisms.
- Examination of mTOR's role in aging and disease models.
- Consideration of clinically approved mTOR-targeting agents.
Main Results:
- Reduced mTOR activity consistently extends lifespan in various organisms, including rodents.
- mTOR signaling is implicated in a wide spectrum of human diseases.
- Pharmacological agents targeting mTOR are available for clinical use.
Conclusions:
- Modulating the mTOR pathway offers promising therapeutic strategies for human aging and disease.
- Understanding mTOR's role in nutrient sensing is key to developing interventions for healthspan.
- Targeting mTOR represents a significant avenue for geroscience research and clinical application.
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