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J. Biol. Chem., Vol. 261, Issue 20, 9128-9132, 07, 1986
LW Daniel, M Waite and RL Wykle
12-O-Tetradecanoylphorbol-13-acetate (TPA) treatment of Madin-Darby canine
kidney cells resulted in an increased incorporation of 32Pi and
[methyl-3H]choline into choline-containing phosphoglycerides (PC). In
pulse-chase experiments, TPA treatment caused an increased release of
[methyl-3H]choline from the PC fraction of prelabeled cells. When cells
were prelabeled with [3H]arachidonic acid and [14C]palmitic acid, TPA
treatment resulted in an increased synthesis of 14C, 3H-diglycerides.
Further studies were done to determine the relationship between PC
breakdown and diglyceride synthesis. Cells were preincubated with ether-
linked 1-O-[3H]hexadecyl-2-lyso-sn-glycero-3-phosphocholine which was
acylated to form 1-O-[3H]hexadecyl-2-acyl-sn-glycero-3-phosphocholine.
Subsequent treatment of these cells with TPA resulted in an increased
synthesis of 1-O-[3H]hexadecyl-2-acyl-sn-glycerol compared to cells not
stimulated with TPA. These findings demonstrate that TPA stimulates PC
turnover in Madin-Darby canine kidney cells and provide evidence for a
novel mechanism of diglyceride formation.
A novel mechanism of diglyceride formation. 12-O-tetradecanoylphorbol- 13-acetate stimulates the cyclic breakdown and resynthesis of phosphatidylcholine
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