Antony P, Kanfer J N, Freysz L
ER 2072 du CNRS-LNMIC-Institut de Chimie Biologique, Faculté de Médecine, Strasbourg, France.
Neurochem Res. 2000 Aug;25(8):1073-82. doi: 10.1023/a:1007613827552.
The agonist stimulation of a variety of cells results in the induction of specific lipid metabolism in nuclear membranes, supporting the hypothesis of an important role of the lipids in nuclear signal transduction. While the existence of a phosphatidylinositol cycle has been reported in cellular nuclei, little attention has been given to the metabolism of phosphatidylcholine in nuclear signaling. In the present study the metabolism of phosphatidylcholine in the nuclei of neuroblastoma cells LA-N-1 was investigated. The incubation of LA-N-1 nuclei with radioactive choline, phosphocholine or CDP-choline led to the production of labelled phosphatidylcholine. The incorporation of choline and phosphocholine but not CDP-choline was enhanced in nuclei of TPA treated cells. Moreover the presence of choline kinase, phosphocholine cytidylyltransferase and phosphocholine transferase activities were detected in the nuclei and the TPA treatment of the cells stimulated the activity of the phosphocholine cytidylyltransferase. When cells prelabelled with [3H]palmitic acid were stimulated with TPA in the presence of ethanol, an increase of labelled diacylglycerol and phosphatidylethanol in the nuclei was observed. Similarly, an increase of labelled diacylglycerol and phosphatidic acid but not of phosphatidylethanol occurred in [3H]palmitic acid prelabelled nuclei stimulated with TPA in the presence of ethanol. However the production of phosphatidylethanol was observed when the nuclei were treated with TPA in the presence of ATP and GTPgammaS. The stimulation of [3H]choline prelabelled nuclei with TPA also generated the release of free choline and phosphocholine. The results indicate the presence of PLD and probably PLC activities in LA-N-1 nuclei and the involvement of phosphatidylcholine in the production of nuclear lipid second messengers upon TPA stimulation of LA-N-1 cells. The correlation of the disappearance of phosphatidylcholine, the production of diacylglycerol and phosphatidic acid with the stimulation of phosphatidylcholine synthesis in nuclei of TPA treated LA-N-1 suggests the existence of a phosphatidylcholine cycle in these nuclei.
多种细胞的激动剂刺激会导致核膜中特定脂质代谢的诱导,这支持了脂质在核信号转导中起重要作用的假说。虽然在细胞核中已报道存在磷脂酰肌醇循环,但磷脂酰胆碱在核信号传导中的代谢却很少受到关注。在本研究中,对神经母细胞瘤细胞LA-N-1细胞核中磷脂酰胆碱的代谢进行了研究。用放射性胆碱、磷酸胆碱或CDP-胆碱孵育LA-N-1细胞核会导致标记的磷脂酰胆碱的产生。TPA处理的细胞的细胞核中胆碱和磷酸胆碱而非CDP-胆碱的掺入增加。此外,在细胞核中检测到胆碱激酶、磷酸胆碱胞苷酰转移酶和磷酸胆碱转移酶的活性,并且细胞的TPA处理刺激了磷酸胆碱胞苷酰转移酶的活性。当用[3H]棕榈酸预标记的细胞在乙醇存在下用TPA刺激时,观察到细胞核中标记的二酰基甘油和磷脂酰乙醇增加。同样,在用[3H]棕榈酸预标记的细胞核中,在乙醇存在下用TPA刺激会导致标记的二酰基甘油和磷脂酸增加,但磷脂酰乙醇不增加。然而,当细胞核在ATP和GTPγS存在下用TPA处理时,观察到磷脂酰乙醇的产生。用TPA刺激[3H]胆碱预标记的细胞核也会导致游离胆碱和磷酸胆碱的释放。结果表明LA-N-1细胞核中存在PLD以及可能的PLC活性,并且在TPA刺激LA-N-1细胞时,磷脂酰胆碱参与核脂质第二信使的产生。TPA处理的LA-N-1细胞核中磷脂酰胆碱的消失、二酰基甘油和磷脂酸的产生与磷脂酰胆碱合成的刺激之间的相关性表明这些细胞核中存在磷脂酰胆碱循环。