Regulation of retinol uptake and esterification in MCF-7 and HepG2 cells by exogenous fatty acids

The influence of extracellular fatty acids on the uptake and esterification of [3H]retinol bound to human retinol-binding protein (RBP), to RBP-transthyretin (TTR), or in dispersed form by the human hepatoma, HepG2, and human mammary epithelial carcinoma, MCF-7, cell lines was studied. The esterific...

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Main Authors: RK Randolph, AC Ross
Format: Article
Language:English
Published: Elsevier 1991-05-01
Series:Journal of Lipid Research
Online Access:http://www.sciencedirect.com/science/article/pii/S0022227520420334
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author RK Randolph
AC Ross
author_facet RK Randolph
AC Ross
author_sort RK Randolph
collection DOAJ
description The influence of extracellular fatty acids on the uptake and esterification of [3H]retinol bound to human retinol-binding protein (RBP), to RBP-transthyretin (TTR), or in dispersed form by the human hepatoma, HepG2, and human mammary epithelial carcinoma, MCF-7, cell lines was studied. The esterification of [3H]retinol was significantly increased in cells incubated with myristic, palmitic, stearic oleic, or linoleic acid-albumin complexes and was observed for all forms of [3H]retinol. Enhancement of [3H]retinol uptake was also observed in cells incubated with these fatty acids, but this increase was relatively small for the dispersed form as compared to that observed for [3H]retinol bound to RBP or RBP-TTR. Comparing equal concentrations of the [3H]retinol donors, cell uptake and esterification was greatest from the dispersed form and least from that bound to RBP-TTR. After preincubation of cells with oleate, uptake and esterification of [3H]retinol was increased but not to the extent observed when oleate and [3H]retinol donor were co-incubated. Incubation of cells with oleate resulted in rapid and correlated increases in the rates of [3H]retinol uptake and esterification which persisted until the steady state for [3H]retinol uptake was achieved. Beyond this time, net esterification of [3H]retinol continued in the presence of oleate. This kinetic pattern was observed for all [3H]retinol donors. These effects on [3H]retinol uptake and esterification were dose-dependent as the oleate to albumin ratio was varied from 0.5 to 3.0 and were observed across a physiological concentration range of RBP-3H-retinol. The data indicate that: 1) the fatty acid status of cells is a determinant of retinol uptake and esterification; and 2) the form of retinol presentation to cells is not qualitatively important for these processes.
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spelling doaj.art-b41b701f06a64001995da6b7854293a72022-12-21T22:47:14ZengElsevierJournal of Lipid Research0022-22751991-05-01325809820Regulation of retinol uptake and esterification in MCF-7 and HepG2 cells by exogenous fatty acidsRK Randolph0AC Ross1Department of Physiology and Biochemistry, Medical College of Pennsylvania, Philadelphia 19129.Department of Physiology and Biochemistry, Medical College of Pennsylvania, Philadelphia 19129.The influence of extracellular fatty acids on the uptake and esterification of [3H]retinol bound to human retinol-binding protein (RBP), to RBP-transthyretin (TTR), or in dispersed form by the human hepatoma, HepG2, and human mammary epithelial carcinoma, MCF-7, cell lines was studied. The esterification of [3H]retinol was significantly increased in cells incubated with myristic, palmitic, stearic oleic, or linoleic acid-albumin complexes and was observed for all forms of [3H]retinol. Enhancement of [3H]retinol uptake was also observed in cells incubated with these fatty acids, but this increase was relatively small for the dispersed form as compared to that observed for [3H]retinol bound to RBP or RBP-TTR. Comparing equal concentrations of the [3H]retinol donors, cell uptake and esterification was greatest from the dispersed form and least from that bound to RBP-TTR. After preincubation of cells with oleate, uptake and esterification of [3H]retinol was increased but not to the extent observed when oleate and [3H]retinol donor were co-incubated. Incubation of cells with oleate resulted in rapid and correlated increases in the rates of [3H]retinol uptake and esterification which persisted until the steady state for [3H]retinol uptake was achieved. Beyond this time, net esterification of [3H]retinol continued in the presence of oleate. This kinetic pattern was observed for all [3H]retinol donors. These effects on [3H]retinol uptake and esterification were dose-dependent as the oleate to albumin ratio was varied from 0.5 to 3.0 and were observed across a physiological concentration range of RBP-3H-retinol. The data indicate that: 1) the fatty acid status of cells is a determinant of retinol uptake and esterification; and 2) the form of retinol presentation to cells is not qualitatively important for these processes.http://www.sciencedirect.com/science/article/pii/S0022227520420334
spellingShingle RK Randolph
AC Ross
Regulation of retinol uptake and esterification in MCF-7 and HepG2 cells by exogenous fatty acids
Journal of Lipid Research
title Regulation of retinol uptake and esterification in MCF-7 and HepG2 cells by exogenous fatty acids
title_full Regulation of retinol uptake and esterification in MCF-7 and HepG2 cells by exogenous fatty acids
title_fullStr Regulation of retinol uptake and esterification in MCF-7 and HepG2 cells by exogenous fatty acids
title_full_unstemmed Regulation of retinol uptake and esterification in MCF-7 and HepG2 cells by exogenous fatty acids
title_short Regulation of retinol uptake and esterification in MCF-7 and HepG2 cells by exogenous fatty acids
title_sort regulation of retinol uptake and esterification in mcf 7 and hepg2 cells by exogenous fatty acids
url http://www.sciencedirect.com/science/article/pii/S0022227520420334
work_keys_str_mv AT rkrandolph regulationofretinoluptakeandesterificationinmcf7andhepg2cellsbyexogenousfattyacids
AT across regulationofretinoluptakeandesterificationinmcf7andhepg2cellsbyexogenousfattyacids