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Coordinated balance of Rac1 and RhoA plays key roles in determining phagocytic appetite
The removal of unwanted or damaged cells by phagocytes is achieved via a finely regulated cleaning process called efferocytosis. To characterize the mechanisms through which phagocytes control the intake of apoptotic cells, we investigated how the phagocyte’s appetite for engulfed cells may be coord...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5380344/ https://www.ncbi.nlm.nih.gov/pubmed/28376111 http://dx.doi.org/10.1371/journal.pone.0174603 |
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author | Kim, Sang-Yeob Kim, Soyoun Bae, Dong-Jun Park, Seung-Yoon Lee, Ga-Young Park, Gyeong-Min Kim, In-San |
author_facet | Kim, Sang-Yeob Kim, Soyoun Bae, Dong-Jun Park, Seung-Yoon Lee, Ga-Young Park, Gyeong-Min Kim, In-San |
author_sort | Kim, Sang-Yeob |
collection | PubMed |
description | The removal of unwanted or damaged cells by phagocytes is achieved via a finely regulated cleaning process called efferocytosis. To characterize the mechanisms through which phagocytes control the intake of apoptotic cells, we investigated how the phagocyte’s appetite for engulfed cells may be coordinated by RhoA and Rac1 in the phagocytic cup. We used FRET biosensors to visualize the spatiotemporal dynamics of Rho-family GTPases, and found that RhoA, which is known to be downregulated during phagocytosis, was transiently upregulated at the phagocytic cup immediately prior to ingestion. Conversely, Rac1 was upregulated during the engulfment process and then downregulated prior to phagosomal maturation. Moreover, disturbance of the dynamic activities of RhoA led to uncontrolled engulfment, such as fast and undiscerning eating. Our results reveal that the temporal activity of RhoA GTPase alters the Rac1/RhoA balance at the phagocytic cup prior to ingestion, and that this plays a distinct role in orchestrating efferocytosis, with RhoA modulating the rate of engulfment to ensure that the phagocyte engulfs an appropriate amount of the correct material. |
format | Online Article Text |
id | pubmed-5380344 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-53803442017-04-19 Coordinated balance of Rac1 and RhoA plays key roles in determining phagocytic appetite Kim, Sang-Yeob Kim, Soyoun Bae, Dong-Jun Park, Seung-Yoon Lee, Ga-Young Park, Gyeong-Min Kim, In-San PLoS One Research Article The removal of unwanted or damaged cells by phagocytes is achieved via a finely regulated cleaning process called efferocytosis. To characterize the mechanisms through which phagocytes control the intake of apoptotic cells, we investigated how the phagocyte’s appetite for engulfed cells may be coordinated by RhoA and Rac1 in the phagocytic cup. We used FRET biosensors to visualize the spatiotemporal dynamics of Rho-family GTPases, and found that RhoA, which is known to be downregulated during phagocytosis, was transiently upregulated at the phagocytic cup immediately prior to ingestion. Conversely, Rac1 was upregulated during the engulfment process and then downregulated prior to phagosomal maturation. Moreover, disturbance of the dynamic activities of RhoA led to uncontrolled engulfment, such as fast and undiscerning eating. Our results reveal that the temporal activity of RhoA GTPase alters the Rac1/RhoA balance at the phagocytic cup prior to ingestion, and that this plays a distinct role in orchestrating efferocytosis, with RhoA modulating the rate of engulfment to ensure that the phagocyte engulfs an appropriate amount of the correct material. Public Library of Science 2017-04-04 /pmc/articles/PMC5380344/ /pubmed/28376111 http://dx.doi.org/10.1371/journal.pone.0174603 Text en © 2017 Kim et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Kim, Sang-Yeob Kim, Soyoun Bae, Dong-Jun Park, Seung-Yoon Lee, Ga-Young Park, Gyeong-Min Kim, In-San Coordinated balance of Rac1 and RhoA plays key roles in determining phagocytic appetite |
title | Coordinated balance of Rac1 and RhoA plays key roles in determining phagocytic appetite |
title_full | Coordinated balance of Rac1 and RhoA plays key roles in determining phagocytic appetite |
title_fullStr | Coordinated balance of Rac1 and RhoA plays key roles in determining phagocytic appetite |
title_full_unstemmed | Coordinated balance of Rac1 and RhoA plays key roles in determining phagocytic appetite |
title_short | Coordinated balance of Rac1 and RhoA plays key roles in determining phagocytic appetite |
title_sort | coordinated balance of rac1 and rhoa plays key roles in determining phagocytic appetite |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5380344/ https://www.ncbi.nlm.nih.gov/pubmed/28376111 http://dx.doi.org/10.1371/journal.pone.0174603 |
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