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在佛波酯处理的C3H10T1/2 Cl 8成纤维细胞中,源自磷脂酰胆碱特异性磷脂酶D的胆碱不能直接用于CDP胆碱途径。

Choline derived from the phosphatidylcholine specific phospholipase D is not directly available for the CDP choline pathway in phorbol ester-treated C3H10T1/2 Cl 8 fibroblasts.

作者信息

Thorsen V A, Bruland O, Lillehaug J R, Holmsen H

机构信息

Department of Biochemistry and Molecular Biology, University of Bergen, Norway.

出版信息

Mol Cell Biochem. 1998 Oct;187(1-2):147-54. doi: 10.1023/a:1006813524791.

Abstract

We have shown that 12-O-tetradecanoylphorbol 13-acetate (TPA) increases protein kinase C (PKC)-mediated choline transport, incorporation of choline into phosphatidylcholine (PtdCho) and PtdCho degradation by phospholipase D (PLD) in C3H10T1/2 Cl 8 cells. Dual prelabeling experiment using [3H]/[14C]choline indicated that intracellular choline generated from the PLD reaction was not directly recycled to PtdCho synthesis within the cell, and that a large fraction of the choline was transported out of the TPA-treated cells. In contrast, medium derived choline was preferably channeled to PtdCho synthesis. These results indicate that in TPA-treated cells, the choline derived from the PKC-mediated increased PLD activity and the choline newly taken up by the cell behave as two distinctly different metabolic pools.

摘要

我们已经证明,在C3H10T1/2 Cl 8细胞中,12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯(TPA)可增加蛋白激酶C(PKC)介导的胆碱转运、胆碱掺入磷脂酰胆碱(PtdCho)以及磷脂酶D(PLD)介导的PtdCho降解。使用[3H]/[14C]胆碱进行的双重预标记实验表明,PLD反应产生的细胞内胆碱不会直接在细胞内循环用于PtdCho合成,并且大部分胆碱会从TPA处理的细胞中转运出去。相比之下,培养基来源的胆碱更倾向于用于PtdCho合成。这些结果表明,在TPA处理的细胞中,PKC介导的PLD活性增加所产生的胆碱与细胞新摄取的胆碱表现为两个明显不同的代谢池。

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