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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
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.
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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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