Molecular Damage Repair encompasses the intrinsic cellular processes dedicated to detecting, correcting, and reversing accumulated damage to essential macromolecules, particularly DNA, proteins, and lipids. This continuous repair work is fundamental to maintaining cellular function and preventing the accumulation of errors that drive aging and age-related diseases. Enhancing these repair mechanisms is a core strategy in longevity medicine and is vital for preserving the integrity of the hormonal signaling apparatus.
Origin
This concept is a cornerstone of molecular biology and gerontology, focusing on the maintenance and stability of the cell’s essential components under constant physiological stress. The term acknowledges that damage is constant and that ‘repair’ is an active, energy-dependent process that determines cellular lifespan.
Mechanism
The mechanism involves a suite of specialized enzyme systems that operate continuously. DNA repair pathways, such as nucleotide excision repair, fix genetic lesions caused by oxidative stress or radiation. Protein damage is mitigated by the proteasome system, which degrades misfolded or damaged proteins, and by chaperones, which assist in correct refolding. These processes are tightly regulated by energy sensors and hormonal signals, such as sirtuins, which link nutrient status to the cell’s capacity for self-maintenance.
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