Senescent Cell Impact refers to the cumulative negative physiological consequences exerted by senescent cells, which are cells that have permanently exited the cell cycle but remain metabolically active and resistant to apoptosis. These cells secrete a pro-inflammatory cocktail of molecules known as the Senescence-Associated Secretory Phenotype (SASP), driving chronic, low-grade systemic inflammation. The impact includes tissue dysfunction, impaired hormonal signaling, and acceleration of the biological aging process.
Origin
The concept is a cornerstone of geroscience, the field linking the biological mechanisms of aging to chronic disease. The term emphasizes the systemic, detrimental effect of these non-proliferating cells, which accumulate with age and contribute to a decline in endocrine function and tissue repair capacity.
Mechanism
The negative impact is primarily mediated by the SASP, which includes pro-inflammatory cytokines, chemokines, and matrix metalloproteinases. These secreted factors disrupt the local tissue microenvironment, impairing the function of adjacent healthy cells and contributing to chronic inflammation, or “inflammaging.” In the context of hormonal health, this chronic inflammation can directly impair receptor sensitivity and disrupt the delicate feedback loops of the hypothalamic-pituitary-adrenal/gonadal axes.
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