Kiss Z, Crilly K S, Anderson W H
The Hormel Institute, University of Minnesota, Austin, MN 55912, USA.
Biochim Biophys Acta. 1998 May 20;1392(1):109-18. doi: 10.1016/s0005-2760(98)00030-7.
The protein kinase C (PKC) activator phorbol 12-myristate 13-acetate (PMA) stimulates both the synthesis and phospholipase D (PLD)-mediated hydrolysis of phosphatidylcholine (PtdCho). Here, attached and suspended NIH 3T3 fibroblasts as well as variants of the MCF-7 human breast carcinoma cell line expressing PKC-alpha and a PtdCho-specific PLD activity at widely different levels were used to determine the possible role of PKC-alpha, PtdCho hydrolysis, and choline uptake in the mediation of PMA effect on PtdCho synthesis. In wild-type MCF-7 cells, which express both PKC-alpha and PLD activities at very low levels, PMA had little effects on the uptake or incorporation [14C]choline into PtdCho. In multidrug resistant MCF-7/MDR1 cells, which highly express PKC-alpha but lack the PtdCho-specific PLD activity, 100-nM PMA had relatively small stimulatory effects on the uptake of [14C]choline (approximately 1.5-fold) and [14C]PtdCho synthesis (1.5- to 2-fold). In NIH 3T3 fibroblasts and MCF-7/PKC-alpha cells, both expressing PKC-alpha and PLD activities at high levels, 10-100-nM PMA enhanced [14C]choline uptake only slightly (1.7- to 2.2-fold), while it had much greater (approximately 4-9-fold) stimulatory effects on PtdCho synthesis. PMA significantly enhanced the formation of phosphatidic acid (PtdOH) in MCF-7/PKC-alpha cells (2.8-fold increase), but not in MCF-7/MDR1 cells (1.4-fold increase), while in both cell lines it had only small (1.3-1.5-fold) stimulatory effects on 1,2-diacylglycerol (1, 2-DAG) formation. In suspended NIH 3T3 cells, 200-300-mM ethanol blocked the stimulatory effect of PMA on PtdOH formation without affecting PtdCho synthesis indicating that neither PtdOH nor 1,2-DAG derived from it is a mediator of PMA effect on PtdCho synthesis. In attached NIH 3T3 cells, dimethylbenz[a]anthracene enhanced phosphocholine formation and, thus, choline uptake without increasing PtdCho synthesis or modifying the effect of PMA. While the results indicate that the stimulatory effect of PMA on PtdCho synthesis requires the expression of both PKC-alpha and a PtdCho-specific PLD, they do not support a role for 1,2-DAG, PtdOH or choline in the mediation of PMA effect.
蛋白激酶C(PKC)激活剂佛波醇12 - 肉豆蔻酸酯13 - 乙酸酯(PMA)可刺激磷脂酰胆碱(PtdCho)的合成以及磷脂酶D(PLD)介导的PtdCho水解。在此,利用贴壁和悬浮的NIH 3T3成纤维细胞以及表达不同水平PKC -α和PtdCho特异性PLD活性的MCF - 7人乳腺癌细胞系变体,来确定PKC -α、PtdCho水解和胆碱摄取在介导PMA对PtdCho合成作用中的可能作用。在野生型MCF - 7细胞中,PKC -α和PLD活性表达水平都非常低,PMA对[14C]胆碱摄取或掺入PtdCho几乎没有影响。在多药耐药的MCF - 7/MDR1细胞中,其高度表达PKC -α但缺乏PtdCho特异性PLD活性,100 nM PMA对[14C]胆碱摄取(约1.5倍)和[14C]PtdCho合成(1.5至2倍)的刺激作用相对较小。在高水平表达PKC -α和PLD活性的NIH 3T3成纤维细胞和MCF - 7/PKC -α细胞中,10 - 100 nM PMA仅略微增强[14C]胆碱摄取(1.7至2.2倍),而对PtdCho合成有更大(约4至9倍)的刺激作用。PMA显著增强了MCF - 7/PKC -α细胞中磷脂酸(PtdOH)的形成(增加2.8倍),但在MCF - 7/MDR1细胞中增强作用较小(增加1.4倍),而在两种细胞系中,它对1,2 - 二酰基甘油(1,2 - DAG)形成的刺激作用都较小(1.3至1.5倍)。在悬浮的NIH 3T3细胞中,200 - 300 mM乙醇阻断了PMA对PtdOH形成的刺激作用,而不影响PtdCho合成,这表明PtdOH及其衍生的1,2 - DAG都不是PMA对PtdCho合成作用的介质。在贴壁的NIH 3T3细胞中,二甲基苯并[a]蒽增强了磷酸胆碱的形成,从而增加了胆碱摄取,但没有增加PtdCho合成或改变PMA的作用。虽然结果表明PMA对PtdCho合成的刺激作用需要PKC -α和PtdCho特异性PLD的表达,但它们不支持1,2 - DAG、PtdOH或胆碱在介导PMA作用中发挥作用。