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The brown adipocyte protein CIDEA promotes lipid droplet fusion via a phosphatidic acid-binding amphipathic helix
Maintenance of energy homeostasis depends on the highly regulated storage and release of triacylglycerol primarily in adipose tissue, and excessive storage is a feature of common metabolic disorders. CIDEA is a lipid droplet (LD)-protein enriched in brown adipocytes promoting the enlargement of LDs,...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4755750/ https://www.ncbi.nlm.nih.gov/pubmed/26609809 http://dx.doi.org/10.7554/eLife.07485 |
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author | Barneda, David Planas-Iglesias, Joan Gaspar, Maria L Mohammadyani, Dariush Prasannan, Sunil Dormann, Dirk Han, Gil-Soo Jesch, Stephen A Carman, George M Kagan, Valerian Parker, Malcolm G Ktistakis, Nicholas T Klein-Seetharaman, Judith Dixon, Ann M Henry, Susan A Christian, Mark |
author_facet | Barneda, David Planas-Iglesias, Joan Gaspar, Maria L Mohammadyani, Dariush Prasannan, Sunil Dormann, Dirk Han, Gil-Soo Jesch, Stephen A Carman, George M Kagan, Valerian Parker, Malcolm G Ktistakis, Nicholas T Klein-Seetharaman, Judith Dixon, Ann M Henry, Susan A Christian, Mark |
author_sort | Barneda, David |
collection | PubMed |
description | Maintenance of energy homeostasis depends on the highly regulated storage and release of triacylglycerol primarily in adipose tissue, and excessive storage is a feature of common metabolic disorders. CIDEA is a lipid droplet (LD)-protein enriched in brown adipocytes promoting the enlargement of LDs, which are dynamic, ubiquitous organelles specialized for storing neutral lipids. We demonstrate an essential role in this process for an amphipathic helix in CIDEA, which facilitates embedding in the LD phospholipid monolayer and binds phosphatidic acid (PA). LD pairs are docked by CIDEA trans-complexes through contributions of the N-terminal domain and a C-terminal dimerization region. These complexes, enriched at the LD–LD contact site, interact with the cone-shaped phospholipid PA and likely increase phospholipid barrier permeability, promoting LD fusion by transference of lipids. This physiological process is essential in adipocyte differentiation as well as serving to facilitate the tight coupling of lipolysis and lipogenesis in activated brown fat. DOI: http://dx.doi.org/10.7554/eLife.07485.001 |
format | Online Article Text |
id | pubmed-4755750 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-47557502016-02-18 The brown adipocyte protein CIDEA promotes lipid droplet fusion via a phosphatidic acid-binding amphipathic helix Barneda, David Planas-Iglesias, Joan Gaspar, Maria L Mohammadyani, Dariush Prasannan, Sunil Dormann, Dirk Han, Gil-Soo Jesch, Stephen A Carman, George M Kagan, Valerian Parker, Malcolm G Ktistakis, Nicholas T Klein-Seetharaman, Judith Dixon, Ann M Henry, Susan A Christian, Mark eLife Biophysics and Structural Biology Maintenance of energy homeostasis depends on the highly regulated storage and release of triacylglycerol primarily in adipose tissue, and excessive storage is a feature of common metabolic disorders. CIDEA is a lipid droplet (LD)-protein enriched in brown adipocytes promoting the enlargement of LDs, which are dynamic, ubiquitous organelles specialized for storing neutral lipids. We demonstrate an essential role in this process for an amphipathic helix in CIDEA, which facilitates embedding in the LD phospholipid monolayer and binds phosphatidic acid (PA). LD pairs are docked by CIDEA trans-complexes through contributions of the N-terminal domain and a C-terminal dimerization region. These complexes, enriched at the LD–LD contact site, interact with the cone-shaped phospholipid PA and likely increase phospholipid barrier permeability, promoting LD fusion by transference of lipids. This physiological process is essential in adipocyte differentiation as well as serving to facilitate the tight coupling of lipolysis and lipogenesis in activated brown fat. DOI: http://dx.doi.org/10.7554/eLife.07485.001 eLife Sciences Publications, Ltd 2015-11-26 /pmc/articles/PMC4755750/ /pubmed/26609809 http://dx.doi.org/10.7554/eLife.07485 Text en © 2015, Barneda et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biophysics and Structural Biology Barneda, David Planas-Iglesias, Joan Gaspar, Maria L Mohammadyani, Dariush Prasannan, Sunil Dormann, Dirk Han, Gil-Soo Jesch, Stephen A Carman, George M Kagan, Valerian Parker, Malcolm G Ktistakis, Nicholas T Klein-Seetharaman, Judith Dixon, Ann M Henry, Susan A Christian, Mark The brown adipocyte protein CIDEA promotes lipid droplet fusion via a phosphatidic acid-binding amphipathic helix |
title | The brown adipocyte protein CIDEA promotes lipid droplet fusion via a phosphatidic acid-binding amphipathic helix |
title_full | The brown adipocyte protein CIDEA promotes lipid droplet fusion via a phosphatidic acid-binding amphipathic helix |
title_fullStr | The brown adipocyte protein CIDEA promotes lipid droplet fusion via a phosphatidic acid-binding amphipathic helix |
title_full_unstemmed | The brown adipocyte protein CIDEA promotes lipid droplet fusion via a phosphatidic acid-binding amphipathic helix |
title_short | The brown adipocyte protein CIDEA promotes lipid droplet fusion via a phosphatidic acid-binding amphipathic helix |
title_sort | brown adipocyte protein cidea promotes lipid droplet fusion via a phosphatidic acid-binding amphipathic helix |
topic | Biophysics and Structural Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4755750/ https://www.ncbi.nlm.nih.gov/pubmed/26609809 http://dx.doi.org/10.7554/eLife.07485 |
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