The ER phagosome connection in the era of membrane contact sites
- PMID: 28432021
- DOI: 10.1016/j.bbamcr.2017.04.007
The ER phagosome connection in the era of membrane contact sites
Abstract
Phagocytosis is an essential mechanism through which innate immune cells ingest foreign material that is either destroyed or used to generate and present antigens and initiate adaptive immune responses. While a role for the ER during phagosome biogenesis has been recognized, whether fusion with ER cisternae or vesicular derivatives occurs has been the source of much contention. Membrane contact sites (MCS) are tight appositions between ER membranes and various organelles that coordinate multiple functions including localized signalling, lipid transfer and trafficking. The discovery that MCS form between the ER and phagosomes now begs the question of whether MCS play a role in connecting the ER to phagosomes under different contexts. In this review, we consider the implications of MCS between the ER and phagosomes during cross-presentation and infection with intracellular pathogens. We also discuss the similarities between these contacts and those between the ER and plasma membrane and acidic organelles such as endosomes and lysosomes. This article is part of a Special Issue entitled: Membrane Contact Sites edited by Christian Ungermann and Benoit Kornmann.
Keywords: Cortical ER; Endoplasmic reticulum; Junctional ER; Legionella pneumophila; Phagocytosis; Toxoplasma gondii.
Copyright © 2017. Published by Elsevier B.V.
Similar articles
-
Quantitative proteomics reveals that only a subset of the endoplasmic reticulum contributes to the phagosome.Mol Cell Proteomics. 2012 Jul;11(7):M111.016378. doi: 10.1074/mcp.M111.016378. Epub 2012 Mar 15. Mol Cell Proteomics. 2012. PMID: 22427703 Free PMC article.
-
Quantitative and dynamic assessment of the contribution of the ER to phagosome formation.Cell. 2005 Oct 7;123(1):157-70. doi: 10.1016/j.cell.2005.08.018. Cell. 2005. PMID: 16213220
-
Junctate boosts phagocytosis by recruiting endoplasmic reticulum Ca2+ stores near phagosomes.J Cell Sci. 2015 Nov 15;128(22):4074-82. doi: 10.1242/jcs.172510. Epub 2015 Oct 7. J Cell Sci. 2015. PMID: 26446257
-
ER-plasma membrane junctions: Why and how do we study them?Biochim Biophys Acta Mol Cell Res. 2017 Sep;1864(9):1494-1506. doi: 10.1016/j.bbamcr.2017.05.018. Epub 2017 May 26. Biochim Biophys Acta Mol Cell Res. 2017. PMID: 28554772 Free PMC article. Review.
-
Endoplasmic reticulum-Phagosome contact sites from the cradle to the grave.Front Cell Dev Biol. 2022 Dec 22;10:1074443. doi: 10.3389/fcell.2022.1074443. eCollection 2022. Front Cell Dev Biol. 2022. PMID: 36619860 Free PMC article. Review.
Cited by
-
Phagocytosis at a glance.J Cell Sci. 2025 Jun 15;138(12):jcs263833. doi: 10.1242/jcs.263833. Epub 2025 Jul 1. J Cell Sci. 2025. PMID: 40590685 Free PMC article. Review.
-
Bone marrow mesenchymal cells: polymorphism associated with transformation of rough endoplasmic reticulum.Blood Sci. 2020 Nov 17;3(1):6-13. doi: 10.1097/BS9.0000000000000062. eCollection 2021 Jan. Blood Sci. 2020. PMID: 35399204 Free PMC article.
-
Molecular Characteristics, Functional Definitions, and Regulatory Mechanisms for Cross-Presentation Mediated by the Major Histocompatibility Complex: A Comprehensive Review.Int J Mol Sci. 2023 Dec 22;25(1):196. doi: 10.3390/ijms25010196. Int J Mol Sci. 2023. PMID: 38203367 Free PMC article. Review.
-
Sec22b regulates phagosome maturation by promoting ORP8-mediated lipid exchange at endoplasmic reticulum-phagosome contact sites.Commun Biol. 2023 Oct 4;6(1):1008. doi: 10.1038/s42003-023-05382-0. Commun Biol. 2023. PMID: 37794132 Free PMC article.
-
Ca2+ Signaling in Exocrine Cells.Cold Spring Harb Perspect Biol. 2020 May 1;12(5):a035279. doi: 10.1101/cshperspect.a035279. Cold Spring Harb Perspect Biol. 2020. PMID: 31636079 Free PMC article. Review.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Other Literature Sources