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Efferocytosis requires periphagosomal Ca(2+)-signaling and TRPM7-mediated electrical activity
Efficient clearance of apoptotic cells by phagocytosis, also known as efferocytosis, is fundamental to developmental biology, organ physiology, and immunology. Macrophages use multiple mechanisms to detect and engulf apoptotic cells, but the signaling pathways that regulate the digestion of the apop...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9184625/ https://www.ncbi.nlm.nih.gov/pubmed/35680919 http://dx.doi.org/10.1038/s41467-022-30959-4 |
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author | Schappe, Michael S. Stremska, Marta E. Busey, Gregory W. Downs, Taylor K. Seegren, Philip V. Mendu, Suresh K. Flegal, Zachary Doyle, Catherine A. Stipes, Eric J. Desai, Bimal N. |
author_facet | Schappe, Michael S. Stremska, Marta E. Busey, Gregory W. Downs, Taylor K. Seegren, Philip V. Mendu, Suresh K. Flegal, Zachary Doyle, Catherine A. Stipes, Eric J. Desai, Bimal N. |
author_sort | Schappe, Michael S. |
collection | PubMed |
description | Efficient clearance of apoptotic cells by phagocytosis, also known as efferocytosis, is fundamental to developmental biology, organ physiology, and immunology. Macrophages use multiple mechanisms to detect and engulf apoptotic cells, but the signaling pathways that regulate the digestion of the apoptotic cell cargo, such as the dynamic Ca(2+) signals, are poorly understood. Using an siRNA screen, we identify TRPM7 as a Ca(2+)-conducting ion channel essential for phagosome maturation during efferocytosis. Trpm7-targeted macrophages fail to fully acidify or digest their phagosomal cargo in the absence of TRPM7. Through perforated patch electrophysiology, we demonstrate that TRPM7 mediates a pH-activated cationic current necessary to sustain phagosomal acidification. Using mice expressing a genetically-encoded Ca(2+) sensor, we observe that phagosome maturation requires peri-phagosomal Ca(2+)-signals dependent on TRPM7. Overall, we reveal TRPM7 as a central regulator of phagosome maturation during macrophage efferocytosis. |
format | Online Article Text |
id | pubmed-9184625 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-91846252022-06-11 Efferocytosis requires periphagosomal Ca(2+)-signaling and TRPM7-mediated electrical activity Schappe, Michael S. Stremska, Marta E. Busey, Gregory W. Downs, Taylor K. Seegren, Philip V. Mendu, Suresh K. Flegal, Zachary Doyle, Catherine A. Stipes, Eric J. Desai, Bimal N. Nat Commun Article Efficient clearance of apoptotic cells by phagocytosis, also known as efferocytosis, is fundamental to developmental biology, organ physiology, and immunology. Macrophages use multiple mechanisms to detect and engulf apoptotic cells, but the signaling pathways that regulate the digestion of the apoptotic cell cargo, such as the dynamic Ca(2+) signals, are poorly understood. Using an siRNA screen, we identify TRPM7 as a Ca(2+)-conducting ion channel essential for phagosome maturation during efferocytosis. Trpm7-targeted macrophages fail to fully acidify or digest their phagosomal cargo in the absence of TRPM7. Through perforated patch electrophysiology, we demonstrate that TRPM7 mediates a pH-activated cationic current necessary to sustain phagosomal acidification. Using mice expressing a genetically-encoded Ca(2+) sensor, we observe that phagosome maturation requires peri-phagosomal Ca(2+)-signals dependent on TRPM7. Overall, we reveal TRPM7 as a central regulator of phagosome maturation during macrophage efferocytosis. Nature Publishing Group UK 2022-06-09 /pmc/articles/PMC9184625/ /pubmed/35680919 http://dx.doi.org/10.1038/s41467-022-30959-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Schappe, Michael S. Stremska, Marta E. Busey, Gregory W. Downs, Taylor K. Seegren, Philip V. Mendu, Suresh K. Flegal, Zachary Doyle, Catherine A. Stipes, Eric J. Desai, Bimal N. Efferocytosis requires periphagosomal Ca(2+)-signaling and TRPM7-mediated electrical activity |
title | Efferocytosis requires periphagosomal Ca(2+)-signaling and TRPM7-mediated electrical activity |
title_full | Efferocytosis requires periphagosomal Ca(2+)-signaling and TRPM7-mediated electrical activity |
title_fullStr | Efferocytosis requires periphagosomal Ca(2+)-signaling and TRPM7-mediated electrical activity |
title_full_unstemmed | Efferocytosis requires periphagosomal Ca(2+)-signaling and TRPM7-mediated electrical activity |
title_short | Efferocytosis requires periphagosomal Ca(2+)-signaling and TRPM7-mediated electrical activity |
title_sort | efferocytosis requires periphagosomal ca(2+)-signaling and trpm7-mediated electrical activity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9184625/ https://www.ncbi.nlm.nih.gov/pubmed/35680919 http://dx.doi.org/10.1038/s41467-022-30959-4 |
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