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Blunting senescence boosts liver regeneration
The mammalian liver possesses a unique capacity for regeneration. However, this regenerative potential declines with age due to unknown mechanisms. In this issue of Genes & Development, Ritschka and colleagues (pp. 489–494). compare liver regeneration upon partial hepatectomy in young and adult...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111267/ https://www.ncbi.nlm.nih.gov/pubmed/32238449 http://dx.doi.org/10.1101/gad.337394.120 |
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author | Birch, Jodie Gil, Jesus |
author_facet | Birch, Jodie Gil, Jesus |
author_sort | Birch, Jodie |
collection | PubMed |
description | The mammalian liver possesses a unique capacity for regeneration. However, this regenerative potential declines with age due to unknown mechanisms. In this issue of Genes & Development, Ritschka and colleagues (pp. 489–494). compare liver regeneration upon partial hepatectomy in young and adult mice. Partial hepatectomy causes a transient increase in p21 in a subpopulation of hepatocytes that persists in adult mice. Remarkably, treatment with the BCL-2 family inhibitor ABT-737 blunts p21 expression, enhancing liver regeneration. |
format | Online Article Text |
id | pubmed-7111267 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-71112672020-10-01 Blunting senescence boosts liver regeneration Birch, Jodie Gil, Jesus Genes Dev Outlook The mammalian liver possesses a unique capacity for regeneration. However, this regenerative potential declines with age due to unknown mechanisms. In this issue of Genes & Development, Ritschka and colleagues (pp. 489–494). compare liver regeneration upon partial hepatectomy in young and adult mice. Partial hepatectomy causes a transient increase in p21 in a subpopulation of hepatocytes that persists in adult mice. Remarkably, treatment with the BCL-2 family inhibitor ABT-737 blunts p21 expression, enhancing liver regeneration. Cold Spring Harbor Laboratory Press 2020-04-01 /pmc/articles/PMC7111267/ /pubmed/32238449 http://dx.doi.org/10.1101/gad.337394.120 Text en © 2020 Birch and Gil; Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first six months after the full-issue publication date (see http://genesdev.cshlp.org/site/misc/terms.xhtml). After six months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Outlook Birch, Jodie Gil, Jesus Blunting senescence boosts liver regeneration |
title | Blunting senescence boosts liver regeneration |
title_full | Blunting senescence boosts liver regeneration |
title_fullStr | Blunting senescence boosts liver regeneration |
title_full_unstemmed | Blunting senescence boosts liver regeneration |
title_short | Blunting senescence boosts liver regeneration |
title_sort | blunting senescence boosts liver regeneration |
topic | Outlook |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111267/ https://www.ncbi.nlm.nih.gov/pubmed/32238449 http://dx.doi.org/10.1101/gad.337394.120 |
work_keys_str_mv | AT birchjodie bluntingsenescenceboostsliverregeneration AT giljesus bluntingsenescenceboostsliverregeneration |