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肿瘤启动子对HeLa细胞中磷脂酰胆碱周转的刺激作用。

Tumor promoter stimulation of phosphatidylcholine turnover in HeLa cells.

作者信息

Guy G R, Murray A W

出版信息

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

PMID:7066909
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.

摘要

将HeLa细胞与[3H]胆碱孵育24小时,导致磷酸胆碱和磷脂酰胆碱池被大量标记。12-O-十四烷酰佛波醇-13-乙酸酯(TPA)、其他佛波酯肿瘤促进剂和芫花酯素刺激了来自此类预先标记细胞的[3H]胆碱和[3H]磷酸胆碱的释放。这种释放伴随着磷酸胆碱池中放射性的降低,这增加了释放的物质是从该池中泄漏而来的可能性。然而,TPA并未诱导含有预先标记的核苷酸池的细胞释放放射性。同样,TPA刺激预先标记细胞释放放射性与磷脂池中而非磷酸胆碱池中的标记密切平行。因此,有人提出释放物质的主要来源是作为磷脂酶C酶底物的磷脂酰胆碱。TPA还模拟了[3H]胆碱掺入磷脂的过程,但一项时间进程研究表明磷脂酶C的激活先于此事件。外源性添加的磷脂酶C也刺激了[3H]胆碱的掺入,这一观察结果支持了上述观点。

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