Studies on the cellular mechanism of free fatty acid uptake using an analog, hexadecanol
Hexadecanol was employed as a fatty acid analog in an attempt to elucidate the role of the carboxyl group in free fatty acid uptake. Large quantities of albumin-bound [1-14C]hexadecanol were taken up by Ehrlich ascites cells during in vitro incubation. More than 90% of the 14C that was taken up rema...
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Format: | Article |
Language: | English |
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Elsevier
1972-11-01
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Series: | Journal of Lipid Research |
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Online Access: | http://www.sciencedirect.com/science/article/pii/S0022227520393500 |
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author | Arthur A. Spector Janice M. Soboroff |
author_facet | Arthur A. Spector Janice M. Soboroff |
author_sort | Arthur A. Spector |
collection | DOAJ |
description | Hexadecanol was employed as a fatty acid analog in an attempt to elucidate the role of the carboxyl group in free fatty acid uptake. Large quantities of albumin-bound [1-14C]hexadecanol were taken up by Ehrlich ascites cells during in vitro incubation. More than 90% of the 14C that was taken up remained as hexadecanol even after 1 hr of incubation at 37°C. Addition of unlabeled hexadecanol did not appreciably alter the rate of [U-14C]glucose oxidation or incorporation into total lipids, suggesting that the slow rate of hexadecanol metabolism was not due to a toxic effect of this analog. However, more of the labeled glucose was incorporated into phospholipids and less into glycerides, indicating that hexadecanol did exert some metabolic effect on the cells. Uptake was temperature dependent but relatively unresponsive to the presence of glucose or fluoride and cyanide. Hexadecanol was incorporated into exchangeable and nonexchangeable cellular pools as determined by its availability for release to a medium containing albumin. These results indicate that a mammalian cell can rapidly take up large amounts of a long-chain hydrocarbon derivative that does not contain a carboxyl group. Furthermore, the data are compatible with the hypothesis that free fatty acids are taken up by a nonenzymatic process such as diffusion into the lipid phase of the cell membrane. |
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format | Article |
id | doaj.art-51140bee8dea4db491bb3d3c1f4f8e04 |
institution | Directory Open Access Journal |
issn | 0022-2275 |
language | English |
last_indexed | 2024-12-14T03:50:55Z |
publishDate | 1972-11-01 |
publisher | Elsevier |
record_format | Article |
series | Journal of Lipid Research |
spelling | doaj.art-51140bee8dea4db491bb3d3c1f4f8e042022-12-21T23:18:13ZengElsevierJournal of Lipid Research0022-22751972-11-01136790796Studies on the cellular mechanism of free fatty acid uptake using an analog, hexadecanolArthur A. Spector0Janice M. Soboroff1Departments of Biochemistry and Internal Medicine, University of Iowa, Iowa City, Iowa 52240Departments of Biochemistry and Internal Medicine, University of Iowa, Iowa City, Iowa 52240Hexadecanol was employed as a fatty acid analog in an attempt to elucidate the role of the carboxyl group in free fatty acid uptake. Large quantities of albumin-bound [1-14C]hexadecanol were taken up by Ehrlich ascites cells during in vitro incubation. More than 90% of the 14C that was taken up remained as hexadecanol even after 1 hr of incubation at 37°C. Addition of unlabeled hexadecanol did not appreciably alter the rate of [U-14C]glucose oxidation or incorporation into total lipids, suggesting that the slow rate of hexadecanol metabolism was not due to a toxic effect of this analog. However, more of the labeled glucose was incorporated into phospholipids and less into glycerides, indicating that hexadecanol did exert some metabolic effect on the cells. Uptake was temperature dependent but relatively unresponsive to the presence of glucose or fluoride and cyanide. Hexadecanol was incorporated into exchangeable and nonexchangeable cellular pools as determined by its availability for release to a medium containing albumin. These results indicate that a mammalian cell can rapidly take up large amounts of a long-chain hydrocarbon derivative that does not contain a carboxyl group. Furthermore, the data are compatible with the hypothesis that free fatty acids are taken up by a nonenzymatic process such as diffusion into the lipid phase of the cell membrane.http://www.sciencedirect.com/science/article/pii/S0022227520393500membranestransportbindingserum albuminEhrlich ascites cellstumor |
spellingShingle | Arthur A. Spector Janice M. Soboroff Studies on the cellular mechanism of free fatty acid uptake using an analog, hexadecanol Journal of Lipid Research membranes transport binding serum albumin Ehrlich ascites cells tumor |
title | Studies on the cellular mechanism of free fatty acid uptake using an analog, hexadecanol |
title_full | Studies on the cellular mechanism of free fatty acid uptake using an analog, hexadecanol |
title_fullStr | Studies on the cellular mechanism of free fatty acid uptake using an analog, hexadecanol |
title_full_unstemmed | Studies on the cellular mechanism of free fatty acid uptake using an analog, hexadecanol |
title_short | Studies on the cellular mechanism of free fatty acid uptake using an analog, hexadecanol |
title_sort | studies on the cellular mechanism of free fatty acid uptake using an analog hexadecanol |
topic | membranes transport binding serum albumin Ehrlich ascites cells tumor |
url | http://www.sciencedirect.com/science/article/pii/S0022227520393500 |
work_keys_str_mv | AT arthuraspector studiesonthecellularmechanismoffreefattyaciduptakeusingananaloghexadecanol AT janicemsoboroff studiesonthecellularmechanismoffreefattyaciduptakeusingananaloghexadecanol |