DIFFERENTIAL-EFFECTS OF UNSATURATED FATTY-ACIDS ON PHOSPHOLIPID-SYNTHESIS IN HUMAN LEUKEMIA MONOCYTIC U937 CELLS

Citation
Aj. Chu et al., DIFFERENTIAL-EFFECTS OF UNSATURATED FATTY-ACIDS ON PHOSPHOLIPID-SYNTHESIS IN HUMAN LEUKEMIA MONOCYTIC U937 CELLS, Cell biochemistry and function, 11(3), 1993, pp. 201-209
Citations number
48
Categorie Soggetti
Biology
ISSN journal
02636484
Volume
11
Issue
3
Year of publication
1993
Pages
201 - 209
Database
ISI
SICI code
0263-6484(1993)11:3<201:DOUFOP>2.0.ZU;2-C
Abstract
The biosynthesis of phosphatidylcholine (PC), and phosphatidylethanola mine (PE) in monocyte-like leukemia U937 cells was monitored by adding [H-3]choline, [C-14]ethanolamine or [C-14]glycerol to the culture med ia; incorporation into phospholipid (PL) increased with time. The effe ct of unsaturated fatty acids (UFA) on PC and PE synthesis was investi gated by pretreating U937 cells for 72 h with 10 mum 18: 1 (n - 9), 18 : 2 (n - 6), 18: 3 (n - 3), 20: 4 (n - 6) and 20: 5 (n - 3). The UFA c aused no alteration in cell growth, as evidenced by light microscopy a nd the incorporation of [H-3]thymidine and [H-3]leucine. Total cellula r uptake of radioactive precursors remained unaffected by all the trea tments. Pretreatment with 20:5 resulted in approximately 25 per cent r eduction in the incorporation of [H-3]choline into PL, while no signif icant effect was detected with the other UFAs. 18:3, 20:4 and 20:5 dep ressed the incorporation of [C-14]ethanolamine into PL by 34 per cent, 28 per cent and 49 per cent respectively. However, there was no redis tribution of label with any of the treatments. 18:3, 20:4 and 20:5 als o antagonized the stimulatory effect of endotoxin (LPS) on PC and PE s ynthesis. In addition, the incorporation from [C-14]glycerol into PC a nd PE was reduced by 18:3, 20:4 and 20:5. Although the PL composition of the cells remained essentially unaffected, our study shows that chr onic treatment of U937 cells with n - 3 PUFA (20:5) depressed PC and P E synthesis, and 18:3 and 20:4 also caused inhibition of PE synthesis.