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ER-Mitochondria Communication in Cells of the Innate Immune System

In cells the interorganelle communication comprises vesicular and non-vesicular mechanisms. Non-vesicular material transfer predominantly takes place at regions of close organelle apposition termed membrane contact sites and is facilitated by a growing number of specialized proteins. Contacts of the...

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Autores principales: Namgaladze, Dmitry, Khodzhaeva, Vera, Brüne, Bernhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6770024/
https://www.ncbi.nlm.nih.gov/pubmed/31540165
http://dx.doi.org/10.3390/cells8091088
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author Namgaladze, Dmitry
Khodzhaeva, Vera
Brüne, Bernhard
author_facet Namgaladze, Dmitry
Khodzhaeva, Vera
Brüne, Bernhard
author_sort Namgaladze, Dmitry
collection PubMed
description In cells the interorganelle communication comprises vesicular and non-vesicular mechanisms. Non-vesicular material transfer predominantly takes place at regions of close organelle apposition termed membrane contact sites and is facilitated by a growing number of specialized proteins. Contacts of the endoplasmic reticulum (ER) and mitochondria are now recognized to be essential for diverse biological processes such as calcium homeostasis, phospholipid biosynthesis, apoptosis, and autophagy. In addition to these universal roles, ER-mitochondria communication serves also cell type-specific functions. In this review, we summarize the current knowledge on ER-mitochondria contacts in cells of the innate immune system, especially in macrophages. We discuss ER- mitochondria communication in the context of macrophage fatty acid metabolism linked to inflammatory and ER stress responses, its roles in apoptotic cell engulfment, activation of the inflammasome, and antiviral defense.
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spelling pubmed-67700242019-10-30 ER-Mitochondria Communication in Cells of the Innate Immune System Namgaladze, Dmitry Khodzhaeva, Vera Brüne, Bernhard Cells Review In cells the interorganelle communication comprises vesicular and non-vesicular mechanisms. Non-vesicular material transfer predominantly takes place at regions of close organelle apposition termed membrane contact sites and is facilitated by a growing number of specialized proteins. Contacts of the endoplasmic reticulum (ER) and mitochondria are now recognized to be essential for diverse biological processes such as calcium homeostasis, phospholipid biosynthesis, apoptosis, and autophagy. In addition to these universal roles, ER-mitochondria communication serves also cell type-specific functions. In this review, we summarize the current knowledge on ER-mitochondria contacts in cells of the innate immune system, especially in macrophages. We discuss ER- mitochondria communication in the context of macrophage fatty acid metabolism linked to inflammatory and ER stress responses, its roles in apoptotic cell engulfment, activation of the inflammasome, and antiviral defense. MDPI 2019-09-15 /pmc/articles/PMC6770024/ /pubmed/31540165 http://dx.doi.org/10.3390/cells8091088 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Namgaladze, Dmitry
Khodzhaeva, Vera
Brüne, Bernhard
ER-Mitochondria Communication in Cells of the Innate Immune System
title ER-Mitochondria Communication in Cells of the Innate Immune System
title_full ER-Mitochondria Communication in Cells of the Innate Immune System
title_fullStr ER-Mitochondria Communication in Cells of the Innate Immune System
title_full_unstemmed ER-Mitochondria Communication in Cells of the Innate Immune System
title_short ER-Mitochondria Communication in Cells of the Innate Immune System
title_sort er-mitochondria communication in cells of the innate immune system
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6770024/
https://www.ncbi.nlm.nih.gov/pubmed/31540165
http://dx.doi.org/10.3390/cells8091088
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