Sierra-Honigmann M R, Bradley J R, Pober J S
Boyer Center for Molecular Medicine, Yale University School of Medicine, New Haven, Connecticut, USA.
Lab Invest. 1996 Mar;74(3):684-95.
The synthesis of arachidonic acid metabolites is initiated by activation of the sn-arachidonyl-dependent, 85-kd "cytosolic" phospholipase A2 (cPLA2) enzyme. We have investigated the subcellular localization of cPLA2 in resting and histamine-treated human and bovine endothelial cells (EC) using confocal immunofluorescence microscopy. In tightly confluent EC, cPLA2 was primarily localized in the cytoplasm. Surprisingly, in subconfluent EC, cPLA2 was also prominently located within the cell nucleus. By immunoblotting of cell lysates after SDS-PAGE, the cytoplasmic molecular species in subconfluent cells displayed the characteristic Mr 110,000, whereas nuclear extracts contained a predominant Mr 70,000. Nuclear localization of cPLA, in subconfluent EC is independent of cell cycle because it was observed in growth-arrested cells as well as in dividing cells. Nuclear localization was also observed in subconfluent MDCK and HeLa cells where, in contrast to EC, it persisted in tightly confluent monolayers. Treatment of subconfluent EC with histamine caused a rapid, dose-dependent redistribution of cPLA2, from the nucleus to the nuclear envelope. The same treatment of confluent EC produced translocation of cytoplasmic enzyme to the nuclear envelope and to the plasma membrane at the intercellular junctions. The cell density dependence of cPLA2, localization may contribute to altered arachidonic acid metabolism in injured vessels as compared with quiescent vessels.
花生四烯酸代谢产物的合成是由sn-花生四烯酰依赖性的85-kd“胞质”磷脂酶A2(cPLA2)酶的激活引发的。我们使用共聚焦免疫荧光显微镜研究了cPLA2在静息和组胺处理的人及牛内皮细胞(EC)中的亚细胞定位。在紧密汇合的EC中,cPLA2主要定位于细胞质中。令人惊讶的是,在亚汇合的EC中,cPLA2也显著位于细胞核内。通过SDS-PAGE后对细胞裂解物进行免疫印迹分析,亚汇合细胞中的细胞质分子种类显示出特征性的Mr 110,000,而核提取物中主要为Mr 70,000。亚汇合EC中cPLA2的核定位与细胞周期无关,因为在生长停滞的细胞以及分裂细胞中均观察到了这种现象。在亚汇合的MDCK和HeLa细胞中也观察到了核定位,与EC不同的是,在紧密汇合的单层细胞中这种定位仍然存在。用组胺处理亚汇合的EC会导致cPLA2迅速、剂量依赖性地从细胞核重新分布到核膜。对汇合的EC进行相同处理会使细胞质酶转移到核膜以及细胞间连接处的质膜。cPLA2定位对细胞密度的依赖性可能导致与静止血管相比,损伤血管中花生四烯酸代谢发生改变。