Resurrection of endogenous retroviruses during aging reinforces senescence
- PMID: 36610399
- DOI: 10.1016/j.cell.2022.12.017
Resurrection of endogenous retroviruses during aging reinforces senescence
Abstract
Whether and how certain transposable elements with viral origins, such as endogenous retroviruses (ERVs) dormant in our genomes, can become awakened and contribute to the aging process is largely unknown. In human senescent cells, we found that HERVK (HML-2), the most recently integrated human ERVs, are unlocked to transcribe viral genes and produce retrovirus-like particles (RVLPs). These HERVK RVLPs constitute a transmissible message to elicit senescence phenotypes in young cells, which can be blocked by neutralizing antibodies. The activation of ERVs was also observed in organs of aged primates and mice as well as in human tissues and serum from the elderly. Their repression alleviates cellular senescence and tissue degeneration and, to some extent, organismal aging. These findings indicate that the resurrection of ERVs is a hallmark and driving force of cellular senescence and tissue aging.
Keywords: HERVK; aging; biomarker; driver; intervention.
Copyright © 2022 The Author(s). Published by Elsevier Inc. All rights reserved.
Conflict of interest statement
Declaration of interests The authors declare no competing interests.
Comment in
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Is aging a "Retro"spective event?Cell. 2023 Jan 19;186(2):233-235. doi: 10.1016/j.cell.2022.12.040. Cell. 2023. PMID: 36669469
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Younger endogenous retroviruses make us older.Nat Rev Mol Cell Biol. 2023 Mar;24(3):165. doi: 10.1038/s41580-023-00580-4. Nat Rev Mol Cell Biol. 2023. PMID: 36670264 No abstract available.
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