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Elimination of Unfit Cells Maintains Tissue Health and Prolongs Lifespan

Viable yet damaged cells can accumulate during development and aging. Although eliminating those cells may benefit organ function, identification of this less fit cell population remains challenging. Previously, we identified a molecular mechanism, based on “fitness fingerprints” displayed on cell m...

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Autores principales: Merino, Marisa M., Rhiner, Christa, Lopez-Gay, Jesus M., Buechel, David, Hauert, Barbara, Moreno, Eduardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4313366/
https://www.ncbi.nlm.nih.gov/pubmed/25601460
http://dx.doi.org/10.1016/j.cell.2014.12.017
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author Merino, Marisa M.
Rhiner, Christa
Lopez-Gay, Jesus M.
Buechel, David
Hauert, Barbara
Moreno, Eduardo
author_facet Merino, Marisa M.
Rhiner, Christa
Lopez-Gay, Jesus M.
Buechel, David
Hauert, Barbara
Moreno, Eduardo
author_sort Merino, Marisa M.
collection PubMed
description Viable yet damaged cells can accumulate during development and aging. Although eliminating those cells may benefit organ function, identification of this less fit cell population remains challenging. Previously, we identified a molecular mechanism, based on “fitness fingerprints” displayed on cell membranes, which allows direct fitness comparison among cells in Drosophila. Here, we study the physiological consequences of efficient cell selection for the whole organism. We find that fitness-based cell culling is naturally used to maintain tissue health, delay aging, and extend lifespan in Drosophila. We identify a gene, azot, which ensures the elimination of less fit cells. Lack of azot increases morphological malformations and susceptibility to random mutations and accelerates tissue degeneration. On the contrary, improving the efficiency of cell selection is beneficial for tissue health and extends lifespan.
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spelling pubmed-43133662015-02-09 Elimination of Unfit Cells Maintains Tissue Health and Prolongs Lifespan Merino, Marisa M. Rhiner, Christa Lopez-Gay, Jesus M. Buechel, David Hauert, Barbara Moreno, Eduardo Cell Article Viable yet damaged cells can accumulate during development and aging. Although eliminating those cells may benefit organ function, identification of this less fit cell population remains challenging. Previously, we identified a molecular mechanism, based on “fitness fingerprints” displayed on cell membranes, which allows direct fitness comparison among cells in Drosophila. Here, we study the physiological consequences of efficient cell selection for the whole organism. We find that fitness-based cell culling is naturally used to maintain tissue health, delay aging, and extend lifespan in Drosophila. We identify a gene, azot, which ensures the elimination of less fit cells. Lack of azot increases morphological malformations and susceptibility to random mutations and accelerates tissue degeneration. On the contrary, improving the efficiency of cell selection is beneficial for tissue health and extends lifespan. Cell Press 2015-01-29 /pmc/articles/PMC4313366/ /pubmed/25601460 http://dx.doi.org/10.1016/j.cell.2014.12.017 Text en © 2015 The Authors http://creativecommons.org/licenses/by/3.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Merino, Marisa M.
Rhiner, Christa
Lopez-Gay, Jesus M.
Buechel, David
Hauert, Barbara
Moreno, Eduardo
Elimination of Unfit Cells Maintains Tissue Health and Prolongs Lifespan
title Elimination of Unfit Cells Maintains Tissue Health and Prolongs Lifespan
title_full Elimination of Unfit Cells Maintains Tissue Health and Prolongs Lifespan
title_fullStr Elimination of Unfit Cells Maintains Tissue Health and Prolongs Lifespan
title_full_unstemmed Elimination of Unfit Cells Maintains Tissue Health and Prolongs Lifespan
title_short Elimination of Unfit Cells Maintains Tissue Health and Prolongs Lifespan
title_sort elimination of unfit cells maintains tissue health and prolongs lifespan
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4313366/
https://www.ncbi.nlm.nih.gov/pubmed/25601460
http://dx.doi.org/10.1016/j.cell.2014.12.017
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