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The formation and function of ER-endosome membrane contact sites()

Recent advances in membrane contact site (MCS) biology have revealed key roles for MCSs in inter-organellar exchange, the importance of which is becoming increasingly apparent. Roles for MCSs in many essential physiological processes including lipid transfer, calcium exchange, receptor tyrosine kina...

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Detalles Bibliográficos
Autor principal: Eden, Emily R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Pub. Co 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4917889/
https://www.ncbi.nlm.nih.gov/pubmed/26898183
http://dx.doi.org/10.1016/j.bbalip.2016.01.020
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author Eden, Emily R.
author_facet Eden, Emily R.
author_sort Eden, Emily R.
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description Recent advances in membrane contact site (MCS) biology have revealed key roles for MCSs in inter-organellar exchange, the importance of which is becoming increasingly apparent. Roles for MCSs in many essential physiological processes including lipid transfer, calcium exchange, receptor tyrosine kinase signalling, lipid droplet formation, autophagosome formation, organelle dynamics and neurite outgrowth have been reported. The ER forms an extensive and dynamic network of MCSs with a diverse range of functionally distinct organelles. MCSs between the ER and endocytic pathway are particularly abundant, suggesting important physiological roles. Here, our current knowledge of the formation and function of ER contact sites with endocytic organelles from studies in mammalian systems is reviewed. Their relatively poorly defined molecular composition and recently identified functions are discussed. In addition, likely, but yet to be established, roles for these contacts in lipid transfer and calcium signalling are considered. This article is part of a Special Issue entitled: The cellular lipid landscape edited by Tim P. Levine and Anant K. Menon.
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spelling pubmed-49178892016-08-01 The formation and function of ER-endosome membrane contact sites() Eden, Emily R. Biochim Biophys Acta Article Recent advances in membrane contact site (MCS) biology have revealed key roles for MCSs in inter-organellar exchange, the importance of which is becoming increasingly apparent. Roles for MCSs in many essential physiological processes including lipid transfer, calcium exchange, receptor tyrosine kinase signalling, lipid droplet formation, autophagosome formation, organelle dynamics and neurite outgrowth have been reported. The ER forms an extensive and dynamic network of MCSs with a diverse range of functionally distinct organelles. MCSs between the ER and endocytic pathway are particularly abundant, suggesting important physiological roles. Here, our current knowledge of the formation and function of ER contact sites with endocytic organelles from studies in mammalian systems is reviewed. Their relatively poorly defined molecular composition and recently identified functions are discussed. In addition, likely, but yet to be established, roles for these contacts in lipid transfer and calcium signalling are considered. This article is part of a Special Issue entitled: The cellular lipid landscape edited by Tim P. Levine and Anant K. Menon. Elsevier Pub. Co 2016-08 /pmc/articles/PMC4917889/ /pubmed/26898183 http://dx.doi.org/10.1016/j.bbalip.2016.01.020 Text en © 2016 The Author http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Eden, Emily R.
The formation and function of ER-endosome membrane contact sites()
title The formation and function of ER-endosome membrane contact sites()
title_full The formation and function of ER-endosome membrane contact sites()
title_fullStr The formation and function of ER-endosome membrane contact sites()
title_full_unstemmed The formation and function of ER-endosome membrane contact sites()
title_short The formation and function of ER-endosome membrane contact sites()
title_sort formation and function of er-endosome membrane contact sites()
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4917889/
https://www.ncbi.nlm.nih.gov/pubmed/26898183
http://dx.doi.org/10.1016/j.bbalip.2016.01.020
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