Senescent Cell Burden represents the cumulative load of non-proliferative, metabolically active cells that have entered a state of irreversible growth arrest, often characterized by the Senescence-Associated Secretory Phenotype (SASP). High burden contributes to chronic low-grade inflammation, tissue dysfunction, and the pathophysiology of numerous age-related diseases. Reducing this burden is a target for rejuvenation science.
Origin
This term originates from cellular aging research, defining senescence as a key driver of biological aging, distinct from simple cell death. The ‘burden’ quantifies the overall impact of these persistent cells on surrounding tissue microenvironments.
Mechanism
Senescent cells secrete pro-inflammatory cytokines, chemokines, and proteases (SASP), which negatively influence neighboring healthy cells and remodel the extracellular matrix detrimentally. Senolytic agents are compounds designed to selectively induce apoptosis in these cells, thereby reducing the chronic inflammatory signaling and improving local tissue function.
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