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Lipid rafts are essential for peroxisome biogenesis in HepG2 cells

โœ Scribed by Jannes Woudenberg; Krzysztof P. Rembacz; Mark Hoekstra; Antonella Pellicoro; Fiona A. J. van den Heuvel; Janette Heegsma; Sven C. D. van IJzendoorn; Andreas Holzinger; Tsuneo Imanaka; Han Moshage; Klaas Nico Faber


Book ID
102850183
Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
802 KB
Volume
52
Category
Article
ISSN
0270-9139

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โœฆ Synopsis


Peroxisomes are particularly abundant in the liver and are involved in bile salt synthesis and fatty acid metabolism. Peroxisomal membrane proteins (PMPs) are required for peroxisome biogenesis [e.g., the interacting peroxisomal biogenesis factors Pex13p and Pex14p] and its metabolic function [e.g., the adenosine triphosphate-binding cassette transporters adrenoleukodystrophy protein (ALDP) and PMP70]. Impaired function of PMPs is the underlying cause of Zellweger syndrome and X-linked adrenoleukodystrophy. Here we studied for the first time the putative association of PMPs with cholesterol-enriched lipid rafts and their function in peroxisome biogenesis. Lipid rafts were isolated from Triton X-100-lysed or Lubrol WX-lysed HepG2 cells and analyzed for the presence of various PMPs by western blotting. Lovastatin and methyl-b-cyclodextrin were used to deplete cholesterol and disrupt lipid rafts in HepG2 cells, and this was followed by immunofluorescence microscopy to determine the subcellular location of catalase and PMPs. Cycloheximide was used to inhibit protein synthesis. Green fluorescent protein-tagged fragments of PMP70 and ALDP were analyzed for their lipid raft association. PMP70 and Pex14p were associated with Triton X-100-resistant rafts, ALDP was associated with Lubrol WX-resistant rafts, and Pex13p was not lipid raft-associated in HepG2 cells. The minimal peroxisomal targeting signals in ALDP and PMP70 were not sufficient for lipid raft association. Cholesterol depletion led to dissociation of PMPs from lipid rafts and impaired sorting of newly synthesized catalase and ALDP but not Pex14p and PMP70. Repletion of cholesterol to these cells efficiently reestablished the peroxisomal sorting of catalase but not ALDP. Conclusion: Human PMPs are differentially associated with lipid rafts independently of the protein homology and/or their functional interaction. Cholesterol is required for peroxisomal lipid raft assembly and peroxisome biogenesis. (HEPATOLOGY 2010;52:623-633) P eroxisomes are single membrane-bound organelles that are especially abundant in the human liver. They are involved in a wide range of meta-bolic processes, including b-oxidation of fatty acids, bile acid biosynthesis, plasmalogen biosynthesis, and the removal of reactive oxygen species that are


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## Abstract Human hepatocellular carcinoma (HepG2) cells take up metallothionein (MT) by endocytosis. MT coโ€localizes with albumin but not with transferrin, indicating uptake via a nonโ€classical pathway rather than via clathrinโ€mediated endocytosis. A lipid raftโ€dependent uptake is indicated by pra