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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...

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Autores principales: Skinner, James R., Harris, Lydia-Ann L.S., Shew, Trevor M., Abumrad, Nada A., Wolins, Nathan E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2013
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.
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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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