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Abstract
Proteome changes during cellular senescence are characterized by widespread protein depletion on chromatin.
- Cellular senescence leads to irreversible cell cycle arrest due to factors like telomere erosion and DNA damage.
- Senescent cells accumulate, disrupting tissue function and contributing to aging and disease.
- The depletion of proteins in the cytoplasmic translation machinery is observed during senescence.
- Mitochondrial proteins in senescent cells show increased insolubility.
- Autophagic and proteasome activities are compromised, along with changes in ubiquitin linkages and depletion of ubiquitin E3 ligases.
- A distinctive senescent proteome signature is identified, differing from other pathological cellular states.
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