Literature DB >> 26416795

Quantitative analysis of the murine lipid droplet-associated proteome during diet-induced hepatic steatosis.

Salmaan Ahmed Khan1, Edith E Wollaston-Hayden1, Todd W Markowski2, LeeAnn Higgins2, Douglas G Mashek3.   

Abstract

Hepatic steatosis is characterized by the accumulation of lipid droplets (LDs), which are composed of a neutral lipid core surrounded by a phospholipid monolayer embedded with many proteins. Although the LD-associated proteome has been investigated in multiple tissues and organisms, the dynamic changes in the murine LD-associated proteome in response to obesity and hepatic steatosis have not been studied. We characterized the hepatic LD-associated proteome of C57BL/6J male mouse livers following high-fat feeding using isobaric tagging for relative and absolute quantification. Of the 1,520 proteins identified with a 5% local false discovery rate, we report a total of 48 proteins that were increased and 52 proteins that were decreased on LDs in response to high-fat feeding. Most notably, ribosomal and endoplasmic reticulum proteins were increased and extracellular and cytosolic proteins were decreased in response to high-fat feeding. Additionally, many proteins involved in fatty acid catabolism or xenobiotic metabolism were enriched in the LD fraction following high-fat feeding. In contrast, proteins involved in glucose metabolism and liver X receptor or retinoid X receptor activation were decreased on LDs of high-fat-fed mice. This study provides insights into unique biological functions of hepatic LDs under normal and steatotic conditions.
Copyright © 2015 by the American Society for Biochemistry and Molecular Biology, Inc.

Entities:  

Keywords:  liver; nutrition; obesity; proteomics; β-oxidation

Mesh:

Substances:

Year:  2015        PMID: 26416795      PMCID: PMC4655982          DOI: 10.1194/jlr.M056812

Source DB:  PubMed          Journal:  J Lipid Res        ISSN: 0022-2275            Impact factor:   5.922


  78 in total

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4.  Chinese hamster ovary K2 cell lipid droplets appear to be metabolic organelles involved in membrane traffic.

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1.  Dgat1 and Dgat2 regulate enterocyte triacylglycerol distribution and alter proteins associated with cytoplasmic lipid droplets in response to dietary fat.

Authors:  Yu-Han Hung; Alicia L Carreiro; Kimberly K Buhman
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Review 5.  [Role of lipophagy in the regulation of lipid metabolism and the molecular mechanism].

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6.  Phosphatidylcholine transfer protein/StarD2 promotes microvesicular steatosis and liver injury in murine experimental steatohepatitis.

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9.  Protein Quality Control and Lipid Droplet Metabolism.

Authors:  Melissa A Roberts; James A Olzmann
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10.  A Luciferase-fragment Complementation Assay to Detect Lipid Droplet-associated Protein-Protein Interactions.

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Journal:  Mol Cell Proteomics       Date:  2016-12-12       Impact factor: 5.911

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