Cellular Replicative Vitality describes the intrinsic capacity of a cell population to undergo a controlled number of successful cell divisions while maintaining functional integrity and genetic stability. This measure reflects the health of the cellular machinery responsible for DNA replication and repair, serving as a key indicator of biological youth and tissue regenerative potential. Declining replicative vitality is directly linked to cellular senescence and the overall aging phenotype.
Origin
The term is rooted in the Hayflick limit theory, which established that normal human cells have a finite number of times they can divide before entering a state of irreversible growth arrest known as senescence. “Replicative” refers to the act of cell duplication, and “vitality” emphasizes the quality and health of this process. It is a concept central to gerontology and regenerative medicine.
Mechanism
The primary mechanism governing this vitality is the maintenance of telomere length by the telomerase enzyme, alongside the efficiency of DNA damage response pathways. Each cell division naturally shortens the telomeres, but sufficient vitality allows for robust repair and management of this attrition. Hormonal factors, such as growth hormone and sex steroids, influence replicative vitality by modulating the cellular environment and promoting anti-senescence signaling.
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