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Journal of Lipid Research, Vol 37, 2098-2108, Copyright © 1996 by Lipid Research, Inc.
S el Bawab, O Macovschi, C Thevenon, A Goncalves, G Nemoz, M Lagarde and AF Prigent
Stimulation of rat thymocytes by concanavalin A (Con A) results in a very
early increase of the cellular level of phosphatidic acid (PA), while that
of diacylglycerol (DAG) was not affected. As the biological activity of PA
is very likely to be determined by its molecular species composition, the
present study aims to investigate the pathways leading to the production of
PA in Con A-stimulated rat thymocytes. Prelabeling the cells with
[3H]arachidonic acid, [3H]myristic acid, [3H]choline, or
[14C]lysophosphatidylcholine allowed us to determine that PA is formed by
both phosphoinositide (PIs) and phosphatidylcholine (PC) hydrolysis. We
then investigated whether PA derived from PC was formed by phospholipase C
(PLC) or phospholipase D (PLD) hydrolysis. In the presence of 1-butanol,
the production of phosphatidylbutanol was only observed in tetradecanoyl
phorbol acetate (TPA)-stimulated cells. The use of a specific PC
phospholipase C inhibitor resulted in a decrease of Con A-stimulated PA
production in cells labeled with [3H]myristate. When cells were labeled
with [3H]choline, only TPA stimulation induced a release of labeled
choline. All together, these experiments suggest that PA is originated from
two phospholipid sources, predominantly PI via PLC hydrolysis and to a
lesser extent PC, by PLC hydrolysis also. Molecular species analyses by
reverse phase HPLC are in agreement with this hypothesis, as diacyl-GP
molecular species composition is similar to that of diacyl-GPC and DAG in
resting cells, but resembles that of diacyl-GPI in Con A-treated cells.
Thus, in stimulated cells, the amount of 18:0/20:4 species doubled while
those of saturated and monounsaturated species decreased.
ARTICLES
Contribution of phosphoinositides and phosphatidylcholines to the production of phosphatidic acid upon concanavalin A stimulation of rat thymocytes
INSERM Unite 352, Laboratoire de Biochimie et Pharmacologie INSA-Lyon, France.
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