Literature DB >> 6954994

Transport of fluorescent derivatives of fatty acids into cultured human leukemic myeloid cells and their subsequent metabolic utilization.

O Morand, E Fibach, A Dagan, S Gatt.   

Abstract

Transport of fluorescent derivatives of fatty acids across the cell membrane of cultured human leukemic myeloid cells (HL 60) and their subsequent metabolic utilization were studied. The rates of uptake of these derivatives and their incorporation into cellular lipids wer compared with that of radioactively labelled palmitic acid. Three groups of fluorescent derivatives were observed: A, those transported into the cells and subsequently incorporated into neutral lipids and phospholipids, B, fatty acids which were taken up by the cells but not utilized metabolically, and C, fatty acids which were not transported across the cell membrane. Fatty acids of the latter group, except the hydrophobic probe, also contained functional groups such as hydroxy, acetylamino or sulfonylamino. When observed in fluorescence microscopy, cells incubated with group A fatty acids contained intracellular fluorescent granules, whereas those incubated with group B fatty acids showed diffuse fluorescence. HL 60 cells undergo differentiation into granulocytes or macrophages upon treatment with dimethylsulfoxide or a phorbol ester, respectively. When compared to the uninduced cells, the transport of the fluorescent fatty acids or palmitic acid as well as their subsequent incorporation into lipids were considerably lower in the granulocytes and higher in the macrophages. The use of the fluorescent derivatives as a tool for studying transport of fatty acids across the cell membrane is discussed.

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Year:  1982        PMID: 6954994     DOI: 10.1016/0005-2760(82)90070-4

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  11 in total

1.  Uptake and degradation of several pyrenesphingomyelins by skin fibroblasts from control subjects and patients with Niemann-Pick disease. Effect of the structure of the fluorescent fatty acyl residue.

Authors:  T Levade; S Gatt; R Salvayre
Journal:  Biochem J       Date:  1991-04-01       Impact factor: 3.857

2.  Influence of chain length of pyrene fatty acids on their uptake and metabolism by Epstein-Barr-virus-transformed lymphoid cell lines from a patient with multisystemic lipid storage myopathy and from control subjects.

Authors:  J Radom; R Salvayre; T Levade; L Douste-Blazy
Journal:  Biochem J       Date:  1990-07-01       Impact factor: 3.857

3.  Rat hepatocyte plasma membrane acyl:CoA synthetase activity.

Authors:  B C Davidson; R C Cantrill
Journal:  Lipids       Date:  1986-09       Impact factor: 1.880

4.  Degradation of pyrene-labelled phospholipids by lysosomal phospholipases in vitro. Dependence of degradation on the length and position of the labelled and unlabelled acyl chains.

Authors:  S Lusa; M Myllärniemi; K Volmonen; M Vauhkonen; P Somerharju
Journal:  Biochem J       Date:  1996-05-01       Impact factor: 3.857

Review 5.  Diversity of fatty acid-binding protein structure and function: studies with fluorescent ligands.

Authors:  J Storch
Journal:  Mol Cell Biochem       Date:  1993 Jun 9-23       Impact factor: 3.396

6.  Enhancement of fluorescence of pyrene-containing lipids by polar media, detergents and phospholipids.

Authors:  T Levade; R Salvayre; S Gatt
Journal:  Experientia       Date:  1987-09-15

7.  Use of pyrenemethyl laurate for fluorescence-based determination of lipase activity in intact living lymphoblastoid cells and for the diagnosis of acid lipase deficiency.

Authors:  A Nègre-Salvayre; A Dagan; S Gatt; R Salvayre
Journal:  Biochem J       Date:  1993-09-15       Impact factor: 3.857

8.  Continuous spectrofluorometric measurements of uptake by cultured cells of 12-(1-pyrene)-dodecanoic acid from its complex with albumin.

Authors:  S Gatt; N Nahas; E Fibach
Journal:  Biochem J       Date:  1988-07-15       Impact factor: 3.857

9.  Uptake of a fluorescent-labeled fatty acid by spiroplasma floricola cells.

Authors:  M Tarshis; M Salman
Journal:  Arch Microbiol       Date:  1992       Impact factor: 2.552

10.  High-throughput screening of Australian marine organism extracts for bioactive molecules affecting the cellular storage of neutral lipids.

Authors:  James Rae; Frank Fontaine; Angela A Salim; Harriet P Lo; Robert J Capon; Robert G Parton; Sally Martin
Journal:  PLoS One       Date:  2011-08-08       Impact factor: 3.240

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