Born this way – Biogenesis of lipid droplets from specialized ER subdomains
Both the endoplasmic reticulum (ER) and lipid droplets (LDs) are key players in lipid handling. In addition to this functional connection, the two organelles are also tightly linked due to the fact that the ER is the birthplace of LDs. LDs have an atypical architecture, consisting of a neutral lipid...
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Veröffentlicht in: | Biochimica et biophysica acta. Molecular and cell biology of lipids 2020-01, Vol.1865 (1), p.158448-158448, Article 158448 |
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container_title | Biochimica et biophysica acta. Molecular and cell biology of lipids |
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creator | Nettebrock, Niclas T. Bohnert, Maria |
description | Both the endoplasmic reticulum (ER) and lipid droplets (LDs) are key players in lipid handling. In addition to this functional connection, the two organelles are also tightly linked due to the fact that the ER is the birthplace of LDs. LDs have an atypical architecture, consisting of a neutral lipid core that is covered by a phospholipid monolayer. LD biogenesis starts with neutral lipid synthesis in the ER membrane and formation of small neutral lipid lenses between its leaflets, followed by budding of mature LDs toward the cytosol.
Several ER proteins have been identified that are required for efficient LD formation, among them seipin, Pex30, and FIT2. Recent evidence indicates that these LD biogenesis factors might cooperate with specific lipids, thus generating ER subdomains optimized for LD assembly. Intriguingly, LD biogenesis reacts dynamically to nutrient stress, resulting in a spatial reorganization of LD formation in the ER.
•Lipid droplets (LDs) are generated from specialized regions of the ER.•ER proteins seipin, Pex30 and FIT2 act as LD biogenesis factors.•LD formation likely depends on a locally optimized membrane environment.•Nutrient stress results in local LD biogenesis at the nucleus-vacuole contact site. |
doi_str_mv | 10.1016/j.bbalip.2019.04.008 |
format | Article |
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Several ER proteins have been identified that are required for efficient LD formation, among them seipin, Pex30, and FIT2. Recent evidence indicates that these LD biogenesis factors might cooperate with specific lipids, thus generating ER subdomains optimized for LD assembly. Intriguingly, LD biogenesis reacts dynamically to nutrient stress, resulting in a spatial reorganization of LD formation in the ER.
•Lipid droplets (LDs) are generated from specialized regions of the ER.•ER proteins seipin, Pex30 and FIT2 act as LD biogenesis factors.•LD formation likely depends on a locally optimized membrane environment.•Nutrient stress results in local LD biogenesis at the nucleus-vacuole contact site.</description><identifier>ISSN: 1388-1981</identifier><identifier>EISSN: 1879-2618</identifier><identifier>DOI: 10.1016/j.bbalip.2019.04.008</identifier><identifier>PMID: 31028912</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Cell Nucleus - metabolism ; Contact site ; Endoplasmic Reticulum - metabolism ; Fat storage inducing transmembrane protein ; Humans ; Lipid droplet organization ; Lipid Droplets - metabolism ; Membrane Proteins - metabolism ; Nucleus vacuole junction ; Pex30 ; Seipin ; Vacuoles - metabolism</subject><ispartof>Biochimica et biophysica acta. Molecular and cell biology of lipids, 2020-01, Vol.1865 (1), p.158448-158448, Article 158448</ispartof><rights>2019 Elsevier B.V.</rights><rights>Copyright © 2019 Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c362t-4e26f087122da038ff48226ace0b3d554c2c297cef7a6501770aec3b97ce533d3</citedby><cites>FETCH-LOGICAL-c362t-4e26f087122da038ff48226ace0b3d554c2c297cef7a6501770aec3b97ce533d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1388198119300617$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31028912$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Nettebrock, Niclas T.</creatorcontrib><creatorcontrib>Bohnert, Maria</creatorcontrib><title>Born this way – Biogenesis of lipid droplets from specialized ER subdomains</title><title>Biochimica et biophysica acta. Molecular and cell biology of lipids</title><addtitle>Biochim Biophys Acta Mol Cell Biol Lipids</addtitle><description>Both the endoplasmic reticulum (ER) and lipid droplets (LDs) are key players in lipid handling. In addition to this functional connection, the two organelles are also tightly linked due to the fact that the ER is the birthplace of LDs. LDs have an atypical architecture, consisting of a neutral lipid core that is covered by a phospholipid monolayer. LD biogenesis starts with neutral lipid synthesis in the ER membrane and formation of small neutral lipid lenses between its leaflets, followed by budding of mature LDs toward the cytosol.
Several ER proteins have been identified that are required for efficient LD formation, among them seipin, Pex30, and FIT2. Recent evidence indicates that these LD biogenesis factors might cooperate with specific lipids, thus generating ER subdomains optimized for LD assembly. Intriguingly, LD biogenesis reacts dynamically to nutrient stress, resulting in a spatial reorganization of LD formation in the ER.
•Lipid droplets (LDs) are generated from specialized regions of the ER.•ER proteins seipin, Pex30 and FIT2 act as LD biogenesis factors.•LD formation likely depends on a locally optimized membrane environment.•Nutrient stress results in local LD biogenesis at the nucleus-vacuole contact site.</description><subject>Animals</subject><subject>Cell Nucleus - metabolism</subject><subject>Contact site</subject><subject>Endoplasmic Reticulum - metabolism</subject><subject>Fat storage inducing transmembrane protein</subject><subject>Humans</subject><subject>Lipid droplet organization</subject><subject>Lipid Droplets - metabolism</subject><subject>Membrane Proteins - metabolism</subject><subject>Nucleus vacuole junction</subject><subject>Pex30</subject><subject>Seipin</subject><subject>Vacuoles - metabolism</subject><issn>1388-1981</issn><issn>1879-2618</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtKxDAUhoMojrc3EMnSTWsuvaQbQWW8gCKIrkOanGqGtqlJRxlXvoNv6JOYYUaXrs7h8P_n5_8QOqQkpYQWJ7O0rlVrh5QRWqUkSwkRG2iHirJKWEHFZty5EAmtBJ2g3RBmhNCc83wbTTglTFSU7aC7c-d7PL7YgN_VAn9_fuFz656hhxBPrsExwRpsvBtaGANuvOtwGEDbmP0BBk8fcJjXxnXK9mEfbTWqDXCwnnvo6XL6eHGd3N5f3Vyc3SaaF2xMMmBFQ0RJGTOKcNE0mWCsUBpIzU2eZ5ppVpUamlIVOaFlSRRoXi9PsYHhe-h49Xfw7nUOYZSdDRraVvXg5kEyRgtWcVHQKM1WUu1dCB4aOXjbKb-QlMglSDmTK5ByCVKSTEaQ0Xa0TpjXHZg_0y-5KDhdCSD2fLPgZdAWeg3GetCjNM7-n_AD19SGUA</recordid><startdate>202001</startdate><enddate>202001</enddate><creator>Nettebrock, Niclas T.</creator><creator>Bohnert, Maria</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>202001</creationdate><title>Born this way – Biogenesis of lipid droplets from specialized ER subdomains</title><author>Nettebrock, Niclas T. ; Bohnert, Maria</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c362t-4e26f087122da038ff48226ace0b3d554c2c297cef7a6501770aec3b97ce533d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animals</topic><topic>Cell Nucleus - metabolism</topic><topic>Contact site</topic><topic>Endoplasmic Reticulum - metabolism</topic><topic>Fat storage inducing transmembrane protein</topic><topic>Humans</topic><topic>Lipid droplet organization</topic><topic>Lipid Droplets - metabolism</topic><topic>Membrane Proteins - metabolism</topic><topic>Nucleus vacuole junction</topic><topic>Pex30</topic><topic>Seipin</topic><topic>Vacuoles - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nettebrock, Niclas T.</creatorcontrib><creatorcontrib>Bohnert, Maria</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Biochimica et biophysica acta. Molecular and cell biology of lipids</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nettebrock, Niclas T.</au><au>Bohnert, Maria</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Born this way – Biogenesis of lipid droplets from specialized ER subdomains</atitle><jtitle>Biochimica et biophysica acta. Molecular and cell biology of lipids</jtitle><addtitle>Biochim Biophys Acta Mol Cell Biol Lipids</addtitle><date>2020-01</date><risdate>2020</risdate><volume>1865</volume><issue>1</issue><spage>158448</spage><epage>158448</epage><pages>158448-158448</pages><artnum>158448</artnum><issn>1388-1981</issn><eissn>1879-2618</eissn><abstract>Both the endoplasmic reticulum (ER) and lipid droplets (LDs) are key players in lipid handling. In addition to this functional connection, the two organelles are also tightly linked due to the fact that the ER is the birthplace of LDs. LDs have an atypical architecture, consisting of a neutral lipid core that is covered by a phospholipid monolayer. LD biogenesis starts with neutral lipid synthesis in the ER membrane and formation of small neutral lipid lenses between its leaflets, followed by budding of mature LDs toward the cytosol.
Several ER proteins have been identified that are required for efficient LD formation, among them seipin, Pex30, and FIT2. Recent evidence indicates that these LD biogenesis factors might cooperate with specific lipids, thus generating ER subdomains optimized for LD assembly. Intriguingly, LD biogenesis reacts dynamically to nutrient stress, resulting in a spatial reorganization of LD formation in the ER.
•Lipid droplets (LDs) are generated from specialized regions of the ER.•ER proteins seipin, Pex30 and FIT2 act as LD biogenesis factors.•LD formation likely depends on a locally optimized membrane environment.•Nutrient stress results in local LD biogenesis at the nucleus-vacuole contact site.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>31028912</pmid><doi>10.1016/j.bbalip.2019.04.008</doi><tpages>1</tpages></addata></record> |
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subjects | Animals Cell Nucleus - metabolism Contact site Endoplasmic Reticulum - metabolism Fat storage inducing transmembrane protein Humans Lipid droplet organization Lipid Droplets - metabolism Membrane Proteins - metabolism Nucleus vacuole junction Pex30 Seipin Vacuoles - metabolism |
title | Born this way – Biogenesis of lipid droplets from specialized ER subdomains |
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