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Perilipin 1 moves between the fat droplet and the endoplasmic reticulum
Perilipin 1, unlike the other perilipins, is thought to be restricted to the fat droplet. We reassessed its cellular distribution using the fat droplet marker CGI-58 in OP9 and 3T3-L1 adipocyte lines and in brown adipose tissue (BAT). As expected, we found perilipin 1 in the fat droplet-enriched flo...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Landes Bioscience
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3661117/ https://www.ncbi.nlm.nih.gov/pubmed/23805403 http://dx.doi.org/10.4161/adip.22864 |
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author | Skinner, James R. Harris, Lydia-Ann L.S. Shew, Trevor M. Abumrad, Nada A. Wolins, Nathan E. |
author_facet | Skinner, James R. Harris, Lydia-Ann L.S. Shew, Trevor M. Abumrad, Nada A. Wolins, Nathan E. |
author_sort | Skinner, James R. |
collection | PubMed |
description | Perilipin 1, unlike the other perilipins, is thought to be restricted to the fat droplet. We reassessed its cellular distribution using the fat droplet marker CGI-58 in OP9 and 3T3-L1 adipocyte lines and in brown adipose tissue (BAT). As expected, we found perilipin 1 in the fat droplet-enriched floating fraction from centrifuged adipocyte or BAT homogenates. However, about half of perilipin 1 was suspended in the cytosol/infranate or pelleted with cellular membranes. In these fractionations, most of the fat droplet-associated protein CGI-58 was in the floating fraction. In BAT and OP9 adipocytes about a third of perilipin 1 pellets, compared with a much smaller fraction of CGI-58. Co-imaging perilipin 1 and smooth endoplasmic reticulum (ER) markers reveals both ER and fat droplet associated perilipin 1 in OP9 adipocytes. Consistent with these observations, perilipin 1 overexpressed in COS7 cells mostly fractionates with cellular membranes and imaging shows it on the ER. In 3T3-L1 adipocytes almost half of perilipin 1 floats, half is suspended as infranate and small amounts pellet. Finally, driving rapid fat droplet synthesis in OP9 adipocytes increases the intensity of perilipin 1 on fat droplets, while decreasing non-fat droplet immunolabeling. Confirming the morphological findings, fractionation shows perilipin 1 moving from the pelleted to the floated fractions. In conclusion, this study documents an expanded intracellular distribution for perilipin 1 and its movement from ER to fat droplet during lipid synthesis. |
format | Online Article Text |
id | pubmed-3661117 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Landes Bioscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-36611172013-06-26 Perilipin 1 moves between the fat droplet and the endoplasmic reticulum Skinner, James R. Harris, Lydia-Ann L.S. Shew, Trevor M. Abumrad, Nada A. Wolins, Nathan E. Adipocyte Research Paper Perilipin 1, unlike the other perilipins, is thought to be restricted to the fat droplet. We reassessed its cellular distribution using the fat droplet marker CGI-58 in OP9 and 3T3-L1 adipocyte lines and in brown adipose tissue (BAT). As expected, we found perilipin 1 in the fat droplet-enriched floating fraction from centrifuged adipocyte or BAT homogenates. However, about half of perilipin 1 was suspended in the cytosol/infranate or pelleted with cellular membranes. In these fractionations, most of the fat droplet-associated protein CGI-58 was in the floating fraction. In BAT and OP9 adipocytes about a third of perilipin 1 pellets, compared with a much smaller fraction of CGI-58. Co-imaging perilipin 1 and smooth endoplasmic reticulum (ER) markers reveals both ER and fat droplet associated perilipin 1 in OP9 adipocytes. Consistent with these observations, perilipin 1 overexpressed in COS7 cells mostly fractionates with cellular membranes and imaging shows it on the ER. In 3T3-L1 adipocytes almost half of perilipin 1 floats, half is suspended as infranate and small amounts pellet. Finally, driving rapid fat droplet synthesis in OP9 adipocytes increases the intensity of perilipin 1 on fat droplets, while decreasing non-fat droplet immunolabeling. Confirming the morphological findings, fractionation shows perilipin 1 moving from the pelleted to the floated fractions. In conclusion, this study documents an expanded intracellular distribution for perilipin 1 and its movement from ER to fat droplet during lipid synthesis. Landes Bioscience 2013-04-01 2013-04-01 /pmc/articles/PMC3661117/ /pubmed/23805403 http://dx.doi.org/10.4161/adip.22864 Text en Copyright © 2013 Landes Bioscience http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Research Paper Skinner, James R. Harris, Lydia-Ann L.S. Shew, Trevor M. Abumrad, Nada A. Wolins, Nathan E. Perilipin 1 moves between the fat droplet and the endoplasmic reticulum |
title | Perilipin 1 moves between the fat droplet and the endoplasmic reticulum |
title_full | Perilipin 1 moves between the fat droplet and the endoplasmic reticulum |
title_fullStr | Perilipin 1 moves between the fat droplet and the endoplasmic reticulum |
title_full_unstemmed | Perilipin 1 moves between the fat droplet and the endoplasmic reticulum |
title_short | Perilipin 1 moves between the fat droplet and the endoplasmic reticulum |
title_sort | perilipin 1 moves between the fat droplet and the endoplasmic reticulum |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3661117/ https://www.ncbi.nlm.nih.gov/pubmed/23805403 http://dx.doi.org/10.4161/adip.22864 |
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