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The different facets of organelle interplay—an overview of organelle interactions

Membrane-bound organelles such as mitochondria, peroxisomes, or the endoplasmic reticulum (ER) create distinct environments to promote specific cellular tasks such as ATP production, lipid breakdown, or protein export. During recent years, it has become evident that organelles are integrated into ce...

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Detalles Bibliográficos
Autores principales: Schrader, Michael, Godinho, Luis F., Costello, Joseph L., Islinger, Markus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4585249/
https://www.ncbi.nlm.nih.gov/pubmed/26442263
http://dx.doi.org/10.3389/fcell.2015.00056
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author Schrader, Michael
Godinho, Luis F.
Costello, Joseph L.
Islinger, Markus
author_facet Schrader, Michael
Godinho, Luis F.
Costello, Joseph L.
Islinger, Markus
author_sort Schrader, Michael
collection PubMed
description Membrane-bound organelles such as mitochondria, peroxisomes, or the endoplasmic reticulum (ER) create distinct environments to promote specific cellular tasks such as ATP production, lipid breakdown, or protein export. During recent years, it has become evident that organelles are integrated into cellular networks regulating metabolism, intracellular signaling, cellular maintenance, cell fate decision, and pathogen defence. In order to facilitate such signaling events, specialized membrane regions between apposing organelles bear distinct sets of proteins to enable tethering and exchange of metabolites and signaling molecules. Such membrane associations between the mitochondria and a specialized site of the ER, the mitochondria associated-membrane (MAM), as well as between the ER and the plasma membrane (PAM) have been partially characterized at the molecular level. However, historical and recent observations imply that other organelles like peroxisomes, lysosomes, and lipid droplets might also be involved in the formation of such apposing membrane contact sites. Alternatively, reports on so-called mitochondria derived-vesicles (MDV) suggest alternative mechanisms of organelle interaction. Moreover, maintenance of cellular homeostasis requires the precise removal of aged organelles by autophagy—a process which involves the detection of ubiquitinated organelle proteins by the autophagosome membrane, representing another site of membrane associated-signaling. This review will summarize the available data on the existence and composition of organelle contact sites and the molecular specializations each site uses in order to provide a timely overview on the potential functions of organelle interaction.
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spelling pubmed-45852492015-10-05 The different facets of organelle interplay—an overview of organelle interactions Schrader, Michael Godinho, Luis F. Costello, Joseph L. Islinger, Markus Front Cell Dev Biol Physiology Membrane-bound organelles such as mitochondria, peroxisomes, or the endoplasmic reticulum (ER) create distinct environments to promote specific cellular tasks such as ATP production, lipid breakdown, or protein export. During recent years, it has become evident that organelles are integrated into cellular networks regulating metabolism, intracellular signaling, cellular maintenance, cell fate decision, and pathogen defence. In order to facilitate such signaling events, specialized membrane regions between apposing organelles bear distinct sets of proteins to enable tethering and exchange of metabolites and signaling molecules. Such membrane associations between the mitochondria and a specialized site of the ER, the mitochondria associated-membrane (MAM), as well as between the ER and the plasma membrane (PAM) have been partially characterized at the molecular level. However, historical and recent observations imply that other organelles like peroxisomes, lysosomes, and lipid droplets might also be involved in the formation of such apposing membrane contact sites. Alternatively, reports on so-called mitochondria derived-vesicles (MDV) suggest alternative mechanisms of organelle interaction. Moreover, maintenance of cellular homeostasis requires the precise removal of aged organelles by autophagy—a process which involves the detection of ubiquitinated organelle proteins by the autophagosome membrane, representing another site of membrane associated-signaling. This review will summarize the available data on the existence and composition of organelle contact sites and the molecular specializations each site uses in order to provide a timely overview on the potential functions of organelle interaction. Frontiers Media S.A. 2015-09-25 /pmc/articles/PMC4585249/ /pubmed/26442263 http://dx.doi.org/10.3389/fcell.2015.00056 Text en Copyright © 2015 Schrader, Godinho, Costello and Islinger. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Schrader, Michael
Godinho, Luis F.
Costello, Joseph L.
Islinger, Markus
The different facets of organelle interplay—an overview of organelle interactions
title The different facets of organelle interplay—an overview of organelle interactions
title_full The different facets of organelle interplay—an overview of organelle interactions
title_fullStr The different facets of organelle interplay—an overview of organelle interactions
title_full_unstemmed The different facets of organelle interplay—an overview of organelle interactions
title_short The different facets of organelle interplay—an overview of organelle interactions
title_sort different facets of organelle interplay—an overview of organelle interactions
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4585249/
https://www.ncbi.nlm.nih.gov/pubmed/26442263
http://dx.doi.org/10.3389/fcell.2015.00056
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