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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,...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2015
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
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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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