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How do red blood cells know when to die?
Human red blood cells (RBCs) are normally phagocytized by macrophages of splenic and hepatic sinusoids at 120 days of age. The destruction of RBCs is ultimately controlled by antagonist effects of phosphatidylserine (PS) and CD47 on the phagocytic activity of macrophages. In this work, we introduce...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society Publishing
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5414242/ https://www.ncbi.nlm.nih.gov/pubmed/28484605 http://dx.doi.org/10.1098/rsos.160850 |
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author | Arias, Clemente Fernandez Arias, Cristina Fernandez |
author_facet | Arias, Clemente Fernandez Arias, Cristina Fernandez |
author_sort | Arias, Clemente Fernandez |
collection | PubMed |
description | Human red blood cells (RBCs) are normally phagocytized by macrophages of splenic and hepatic sinusoids at 120 days of age. The destruction of RBCs is ultimately controlled by antagonist effects of phosphatidylserine (PS) and CD47 on the phagocytic activity of macrophages. In this work, we introduce a conceptual model that explains RBC lifespan as a consequence of the dynamics of these molecules. Specifically, we suggest that PS and CD47 define a molecular algorithm that sets the timing of RBC phagocytosis. We show that significant changes in RBC lifespan described in the literature can be explained as alternative outcomes of this algorithm when it is executed in different conditions of oxygen availability. The theoretical model introduced here provides a unified framework to understand a variety of empirical observations regarding RBC biology. It also highlights the role of RBC lifespan as a key element of RBC homeostasis. |
format | Online Article Text |
id | pubmed-5414242 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Royal Society Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-54142422017-05-08 How do red blood cells know when to die? Arias, Clemente Fernandez Arias, Cristina Fernandez R Soc Open Sci Cellular and Molecular Biology Human red blood cells (RBCs) are normally phagocytized by macrophages of splenic and hepatic sinusoids at 120 days of age. The destruction of RBCs is ultimately controlled by antagonist effects of phosphatidylserine (PS) and CD47 on the phagocytic activity of macrophages. In this work, we introduce a conceptual model that explains RBC lifespan as a consequence of the dynamics of these molecules. Specifically, we suggest that PS and CD47 define a molecular algorithm that sets the timing of RBC phagocytosis. We show that significant changes in RBC lifespan described in the literature can be explained as alternative outcomes of this algorithm when it is executed in different conditions of oxygen availability. The theoretical model introduced here provides a unified framework to understand a variety of empirical observations regarding RBC biology. It also highlights the role of RBC lifespan as a key element of RBC homeostasis. The Royal Society Publishing 2017-04-05 /pmc/articles/PMC5414242/ /pubmed/28484605 http://dx.doi.org/10.1098/rsos.160850 Text en © 2017 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Cellular and Molecular Biology Arias, Clemente Fernandez Arias, Cristina Fernandez How do red blood cells know when to die? |
title | How do red blood cells know when to die? |
title_full | How do red blood cells know when to die? |
title_fullStr | How do red blood cells know when to die? |
title_full_unstemmed | How do red blood cells know when to die? |
title_short | How do red blood cells know when to die? |
title_sort | how do red blood cells know when to die? |
topic | Cellular and Molecular Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5414242/ https://www.ncbi.nlm.nih.gov/pubmed/28484605 http://dx.doi.org/10.1098/rsos.160850 |
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