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. 1982 May;42(5):1980-5.

Tumor promoter stimulation of phosphatidylcholine turnover in HeLa cells

  • PMID: 7066909

Tumor promoter stimulation of phosphatidylcholine turnover in HeLa cells

G R Guy et al. Cancer Res. 1982 May.

Abstract

Incubation of HeLa cells for 24 hr with [3H]choline resulted in extensive labeling of the phosphorylcholine and phosphatidylcholine pools. 12-O-Tetradecanoylphorbol-13-acetate (TPA), other phorbol ester tumor promoters, and mezerein stimulated the release of [3H]choline and [3H]phosphorylcholine from such prelabeled cells. The release was accompanied by decreased radioactivity in the phosphorylcholine pool, raising the possibility that the released materials were derived by leakage from this pool. However, TPA did not induce the release of radioactivity from cells containing a prelabeled nucleotide pool. Similarly, the TPA-stimulated release of radioactivity from prelabeled cells closely paralleled the label present in the phospholipid pool rather than the phosphocholine pool. Consequently, it is suggested that the primary source of the released material is phosphatidylcholine acting as a substrate for a phospholipase C enzyme. TPA also simulated the incorporation of [3H]choline into phospholipids, but a time-course study indicated that phospholipase C activation preceded this event. This was supported by the observation that incorporation of [3H]choline was also stimulated by exogenously added phospholipase C.

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