Abstract

Phosphatidic acid generation through activation of diacylglycerol kinase alpha has been implicated in interleukin-2-dependent T-lymphocyte proliferation. To investigate this lipid signaling in more detail, we characterized the molecular structures of the diradylglycerols and phosphatidic acids in the murine CTLL-2 T-cell line under both basal and stimulated conditions. In resting cells, 1,2-diacylglycerol and 1-O-alkyl-2-acylglycerol subtypes represented 44 and 55% of total diradylglycerol, respectively, and both showed a highly saturated profile containing primarily 16:0 and 18:1 fatty acids. 1-O-Alk-1'-enyl-2-acylglycerol represented 1-2% of total diradylglycerol. Interleukin-2 stimulation did not alter the molecular species profiles, however, it did selectively reduce total 1-O-alkyl-2-acylglycerol by over 50% at 15 min while only causing a 10% drop in 1,2-diacylglycerol. When radiolabeled CTLL-2 cells were challenged with interleukin-2, no change in the cellular content of phosphatidylcholine nor phosphatidylethanolamine was observed thereby ruling out phospholipase C activity as the source of diradylglycerol. In addition, interleukin-2 failed to stimulate de novo synthesis of diradylglycerol. Structural analysis revealed approximately equal amounts of 1,2-diacyl phosphatidic acid and 1-O-alkyl-2-acyl phosphatidic acid under resting conditions, both containing only saturated and monounsaturated fatty acids. After acute (2 and 15 min) interleukin-2 stimulation the total phosphatidic acid mass increased, almost entirely through the formation of 1-O-alkyl-2-acyl species. In vitro assays revealed that both 1,2-diacylglycerol and 1-O-alkyl-2-acylglycerol were substrates for 1,2-diacylglycerol kinase alpha, the major isoform in CTLL-2 cells, and that the lipid kinase activity was almost totally inhibited by R59949. In conclusion, this investigation shows that, in CTLL-2 cells, 1,2-diacylglycerol kinase alpha specifically phosphorylates a pre-existing pool of 1-O-alkyl-2-acylglycerol to form the intracellular messenger 1-O-alkyl-2-acyl phosphatidic acid.

Highlights

  • Phosphatidic acid generation through activation of diacylglycerol kinase ␣ has been implicated in interleukin-2dependent T-lymphocyte proliferation

  • Structural analysis of precursor phospholipids and lipid second messengers (LSMs) have demonstrated that phospholipid hydrolysis by activated phospholipases is not a random process, but rather is highly organized and selective for particular lipid classes leading to the formation of specific LSMs (4 –7)

  • No di- or more unsaturated fatty acids were found in CTLL-2 cell phosphatidic acid (PA)

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Summary

EXPERIMENTAL PROCEDURES

Materials—Human recombinant IL-2 was a generous gift from Hoffman-LaRoche Inc. (Nutley, NJ). [␥-32P]ATP (specific activity 3000 Ci/ mmol), 1-O-[3H]octadecyl lysophosphatidylcholine (specific activity 110 –210 Ci/mmol), D-[U-14C]glucose (specific activity 230 –370 mCi/ mmol), and [9,10-3H]oleic acid (specific activity 2–10 Ci/mmol) were purchased from Amersham (Amersham, United Kingdom). Cells (2 ϫ 106) were incubated Ϯ 500 units/ml IL-2 for various times, pelleted and immediately frozen on dry ice. Total lipids were extracted, [17], followed by the separation of [3H]1-O-alkyl-2-acyl-PC (AAG-PC) and [3H]1-O-alkyl-2acyl-PE (AAG-PE) by TLC using a solvent system consisting of propan1-ol/propionic acid/chloroform/water (60/40/40/20, by volume). Cell incubations were terminated by the rapid addition of 9 volumes of ice-cold phosphate-buffered saline, containing 1% BSA followed by cell centrifugation and freezing of the pellets on dry ice. After total lipid extraction [17], the DRG was separated from all other neutral lipids by TLC using the solvent system composed of petroleum ether/diethyl ether/glacial acetic acid (70/30/2, v/v/v). Radioactivity within the DRG fraction of the CTLL-2 cells (comigrating with authentic 1,2-dioleoylglycerol standard) was determined as described above

RESULTS
Peak number
Flux through PAP
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