Cellular Longevity Signaling encompasses the complex intracellular pathways that regulate the lifespan, maintenance, and programmed death of somatic cells, directly impacting tissue health and resilience against aging. Optimizing these signals is critical for maintaining the functional integrity of endocrine glands and target tissues over time. When these signals falter, cellular senescence increases, contributing to chronic inflammation and impaired hormone responsiveness. We aim to support the intrinsic programming for cellular self-renewal.
Origin
This concept merges fundamental cell biology, focusing on the mechanics of cell survival, with gerontology, the study of aging. It acknowledges that aging is fundamentally programmed at the molecular level within each cell type. The signal aspect refers to the molecular cascades that communicate survival or apoptotic instructions.
Mechanism
Key mechanisms involve the sirtuin family of deacetylases, which are activated by NAD+ availability and promote DNA repair and genomic stability. Furthermore, the mTOR pathway acts as a central nutrient sensor, where suppression often promotes autophagy and cellular housekeeping, extending functional lifespan. Supporting these pathways through metabolic control or targeted nutrient intervention helps maintain a youthful cellular phenotype capable of responding appropriately to hormonal cues.
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