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PMID: 15897193 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Lipid droplets gain PAT family proteins by interaction with specialized plasma membrane domains.

The Journal of biological chemistry ·Vol. 280 ·No. 28 ·2005-07-15 ·Pages 26330-8

Robenek H, Robenek MJ, Buers I, Lorkowski S, Hofnagel O, Troyer D, Severs NJ

Abstract

Proteins of the PAT family, named after perilipin, adipophilin, and TIP47 (tail-interacting protein of 47 kDa), are associated with lipid droplets and have previously been localized by immunofluorescence microscopy exclusively to the droplet surface. These proteins are considered not to be present in any other subcellular compartment. By applying the high resolution technique of freeze-fracture electron microscopy combined with immunogold labeling, we now demonstrate that in macrophages and adipocytes PAT family proteins are, first, distributed not only in the surface but also throughout the lipid droplet core and, second, are integral components of the plasma membrane. Under normal culture conditions these proteins are dispersed in the cytoplasmic leaflet of the plasma membrane. Stimulation of lipid droplet formation by incubation of the cells with acetylated low density lipoprotein leads to clustering of the PAT family proteins in raised plasma membrane domains. Fractures penetrating beneath the plasma membrane demonstrate that lipid droplets are closely apposed to these domains. A similar distribution pattern of labeling in the form of linear aggregates within the clusters is apparent in the cytoplasmic monolayer of the plasma membrane and the immediately adjacent outer monolayer of the lipid droplet. The aggregation of the PAT family proteins into such assemblies may facilitate carrier-mediated lipid influx from the extracellular environment into the lipid droplet. Lipid droplets appear to acquire their PAT proteins by interaction with plasma membrane domains enriched in these proteins.

MeSH Terms
3T3-L1 Cells Adipocytes/metabolism,ultrastructure Animals Carrier Proteins Caveolin 1 Caveolins/metabolism Cell Line Cell Membrane/metabolism DNA-Binding Proteins/chemistry Freeze Fracturing Humans Immunohistochemistry Intracellular Signaling Peptides and Proteins/chemistry Lipids/chemistry Macrophages/metabolism Membrane Proteins Mice Microscopy, Confocal Microscopy, Electron Microscopy, Fluorescence Monocytes/metabolism Peptides/chemistry Perilipin-1 Perilipin-2 Perilipin-3 Phosphoproteins/chemistry Pregnancy Proteins/chemistry Protein Binding Protein Structure, Tertiary Vesicular Transport Proteins
Chemicals
Carrier Proteins Caveolin 1 Caveolins DNA-Binding Proteins Intracellular Signaling Peptides and Proteins Lipids Membrane Proteins PLIN2 protein, human PLIN3 protein, human Peptides Perilipin-1 Perilipin-2 Perilipin-3 Phosphoproteins Plin2 protein, mouse Pregnancy Proteins Vesicular Transport Proteins
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Robenek Horst
Department of Cell Biology and Ultrastructure Research, Leibniz-Institute for Arteriosclerosis Research, University of Münster, Münster, Germany. robenek@uni-muenster.de
Robenek Mirko J
Buers Insa
Lorkowski Stefan
Hofnagel Oliver
Troyer David
Severs Nicholas J
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2005-07-15
Epub
2005-00-16
Pages
26330-8
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
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