Imaging cytoplasmic lipid droplets in vivo with fluorescent perilipin 2 and perilipin 3 knock-in zebrafish

Cytoplasmic lipid droplets are highly dynamic storage organelles that are critical for cellular lipid homeostasis. While the molecular details of lipid droplet dynamics are a very active area of investigation, this work has been primarily performed in cultured cells. Taking advantage of the powerful...

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Main Authors: Meredith H Wilson, Stephen C Ekker, Steven A Farber
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2021-08-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/66393
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spelling doaj-46058fdd397a40a9828b3b8699040bfe2021-09-23T10:10:04ZengeLife Sciences Publications LtdeLife2050-084X2021-08-011010.7554/eLife.66393Imaging cytoplasmic lipid droplets in vivo with fluorescent perilipin 2 and perilipin 3 knock-in zebrafishMeredith H Wilson0https://orcid.org/0000-0002-6152-7127Stephen C Ekker1https://orcid.org/0000-0003-0726-4212Steven A Farber2https://orcid.org/0000-0002-8037-7312Carnegie Institution for Science Department of Embryology, Baltimore, United StatesDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, United StatesCarnegie Institution for Science Department of Embryology, Baltimore, United States; Johns Hopkins University Department of Biology, Baltimore, United StatesCytoplasmic lipid droplets are highly dynamic storage organelles that are critical for cellular lipid homeostasis. While the molecular details of lipid droplet dynamics are a very active area of investigation, this work has been primarily performed in cultured cells. Taking advantage of the powerful transgenic and in vivo imaging opportunities available in zebrafish, we built a suite of tools to study lipid droplets in real time from the subcellular to the whole organism level. Fluorescently tagging the lipid droplet-associated proteins, perilipin 2 and perilipin 3, in the endogenous loci permits visualization of lipid droplets in the intestine, liver, and adipose tissue. Using these tools, we found that perilipin 3 is rapidly loaded on intestinal lipid droplets following a high-fat meal and later replaced by perilipin 2. These powerful new tools will facilitate studies on the role of lipid droplets in different tissues, under different genetic and physiological manipulations, and in a variety of human disease models.https://elifesciences.org/articles/66393lipid dropletperilipinPLIN
collection DOAJ
language English
format Article
sources DOAJ
author Meredith H Wilson
Stephen C Ekker
Steven A Farber
spellingShingle Meredith H Wilson
Stephen C Ekker
Steven A Farber
Imaging cytoplasmic lipid droplets in vivo with fluorescent perilipin 2 and perilipin 3 knock-in zebrafish
eLife
lipid droplet
perilipin
PLIN
author_facet Meredith H Wilson
Stephen C Ekker
Steven A Farber
author_sort Meredith H Wilson
title Imaging cytoplasmic lipid droplets in vivo with fluorescent perilipin 2 and perilipin 3 knock-in zebrafish
title_short Imaging cytoplasmic lipid droplets in vivo with fluorescent perilipin 2 and perilipin 3 knock-in zebrafish
title_full Imaging cytoplasmic lipid droplets in vivo with fluorescent perilipin 2 and perilipin 3 knock-in zebrafish
title_fullStr Imaging cytoplasmic lipid droplets in vivo with fluorescent perilipin 2 and perilipin 3 knock-in zebrafish
title_full_unstemmed Imaging cytoplasmic lipid droplets in vivo with fluorescent perilipin 2 and perilipin 3 knock-in zebrafish
title_sort imaging cytoplasmic lipid droplets in vivo with fluorescent perilipin 2 and perilipin 3 knock-in zebrafish
publisher eLife Sciences Publications Ltd
series eLife
issn 2050-084X
publishDate 2021-08-01
description Cytoplasmic lipid droplets are highly dynamic storage organelles that are critical for cellular lipid homeostasis. While the molecular details of lipid droplet dynamics are a very active area of investigation, this work has been primarily performed in cultured cells. Taking advantage of the powerful transgenic and in vivo imaging opportunities available in zebrafish, we built a suite of tools to study lipid droplets in real time from the subcellular to the whole organism level. Fluorescently tagging the lipid droplet-associated proteins, perilipin 2 and perilipin 3, in the endogenous loci permits visualization of lipid droplets in the intestine, liver, and adipose tissue. Using these tools, we found that perilipin 3 is rapidly loaded on intestinal lipid droplets following a high-fat meal and later replaced by perilipin 2. These powerful new tools will facilitate studies on the role of lipid droplets in different tissues, under different genetic and physiological manipulations, and in a variety of human disease models.
topic lipid droplet
perilipin
PLIN
url https://elifesciences.org/articles/66393
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AT stephencekker imagingcytoplasmiclipiddropletsinvivowithfluorescentperilipin2andperilipin3knockinzebrafish
AT stevenafarber imagingcytoplasmiclipiddropletsinvivowithfluorescentperilipin2andperilipin3knockinzebrafish
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