PMID:16204232

Citation	Maric, J, Kiss, RS, Franklin, V and Marcel, YL (2005) Intracellular lipidation of newly synthesized apolipoprotein A-I in primary murine hepatocytes. J. Biol. Chem. 280:39942-9
Abstract	Hepatocytes, which are the main site of apolipoprotein (apo)A-I and ATP-binding cassette transporter A1 (ABCA1) expression, are also the main source of circulating high density lipoprotein. Here we have characterized the intracellular lipidation of newly synthesized apoA-I, in primary hepatocytes cultured with [3H]choline to label choline-phospholipids, low density lipoprotein-[3H]cholesterol to label the cell surface, or [3H]mevalonate to label de novo synthesized cholesterol. Phospholipidation of apoA-I is significant and most evident in endoplasmic reticulum (ER) and medial Golgi, both in the lumen and on the membrane fractions of the ER and medial Golgi. In the presence of cycloheximide, endogenous apoA-I is substantially phospholipidated intracellularly but acquires some additional lipid after export out of the cell. In cells labeled with low density lipoprotein-[3H]cholesterol, intracellular cholesterol lipidation of apoA-I is entirely absent, but the secreted apoA-I rapidly accumulates cholesterol after secretion from the cell in the media. On the other hand, de novo synthesized cholesterol can lipidate apoA-I intracellularly. We also showed the interaction between apoA-I and ABCA1 in ER and Golgi fractions. In hepatocytes lacking ABCA1, lipidation by low density lipoprotein-cholesterol was significantly reduced at the plasma membrane, phospholipidation and lipidation by de novo synthesized sterols were both reduced in Golgi compartments, whereas ER lipidation remained mostly unchanged. Therefore, the early lipidation in ER is ABCA1 independent, but in contrast, the lipidation of apoA-I in Golgi and at the plasma membrane requires ABCA1. Thus, we demonstrated that apoA-I phospholipidation starts early in the ER and is partially dependent on ABCA1, with the bulk of lipidation by phospholipids and cholesterol occurring in the Golgi and at the plasma membrane, respectively. Finally, we showed that the previously reported association of newly synthesized apoA-I and apoB (Zheng, H., Kiss, R. S., Franklin, V., Wang, M. D., Haidar, B., and Marcel, Y. L. (2005) J. Biol. Chem. 280, 21612-21621) occurs after secretion at the cell surface.
Links	PubMed Online version:10.1074/jbc.M507733200
Keywords	ATP-Binding Cassette Transporters/metabolism; Animals; Apolipoprotein A-I/chemistry; Blotting, Western; Cell Membrane/metabolism; Cells, Cultured; Cholesterol/metabolism; Cholesterol, LDL/chemistry; Choline/chemistry; Chromatography, Gas; Chromatography, Thin Layer; Cycloheximide/pharmacology; Endoplasmic Reticulum/metabolism; Golgi Apparatus/metabolism; Hepatocytes/cytology; Hepatocytes/metabolism; Immunoprecipitation; Iohexol/pharmacology; Lipid Metabolism; Lipids/chemistry; Lipoproteins/chemistry; Lipoproteins, HDL/chemistry; Lipoproteins, LDL/chemistry; Lipoproteins, LDL/metabolism; Mice; Mice, Inbred C57BL; Mice, Knockout; Mice, Transgenic; Phosphatidylcholines/chemistry; Protein Synthesis Inhibitors/pharmacology; Sphingomyelins/chemistry; Subcellular Fractions/metabolism; Time Factors
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