Wu M H, Lam C Y, Yung B Y
Graduate Institute of Pharmacology, Yang Ming Medical College, Taiwan, Republic of China.
Biochem J. 1995 Feb 1;305 ( Pt 3)(Pt 3):987-92. doi: 10.1042/bj3050987.
The movement of nucleophosmin from nucleoli to nucleoplasm in HeLa cells induced by cytotoxic drugs and detected by immunofluorescence is inhibited by concomitant treatment with antimycin A in glucose-free medium. Incubation of HeLa cells with antimycin A (300 nM; 30 min) and glucose-free medium resulted in an approximately 90% decrease in cellular ATP pools. To study the biochemical events involved in nucleophosmin translocation, we used an in vitro system consisting of Triton-permeabilized HeLA cells. Incubation of permeabilized cells with ATP (0.5 mM; 1 h) resulted in the translocation of nucleophosmin from nucleoli to nucleoplasm and cytoplasm. Similarly to drug-induced nucleophosmin translocation in whole cultured cells, there is no reduction (measured by e.l.i.s.a.) or degradation of nucleophosmin or change in the ratio of the high-molecular-mass form to the monomeric form (ascertained by Western blotting) during ATP treatment of permeabilized cells. Together, these results indicate a requirement for ATP for redistribution of nucleophosmin from nucleoli to nucleoplasm. Because this permeabilized cell model is simple and efficient and works effectively with exogenous factors, it should provide a powerful tool for investigating the biochemical features of nucleophosmin translocation from nucleoli to nucleoplasm.
在无葡萄糖培养基中,抗霉素A的协同处理可抑制细胞毒性药物诱导的HeLa细胞中核磷蛋白从核仁向核质的移动(通过免疫荧光检测)。用抗霉素A(300 nM;30分钟)和无葡萄糖培养基孵育HeLa细胞,导致细胞ATP池减少约90%。为了研究核磷蛋白易位所涉及的生化事件,我们使用了由Triton通透的HeLa细胞组成的体外系统。用ATP(0.5 mM;1小时)孵育通透细胞导致核磷蛋白从核仁易位到核质和细胞质。与全培养细胞中药物诱导的核磷蛋白易位类似,在通透细胞的ATP处理过程中,核磷蛋白没有减少(通过酶联免疫吸附测定法测量)或降解,高分子量形式与单体形式的比例也没有变化(通过蛋白质印迹法确定)。总之,这些结果表明核磷蛋白从核仁重新分布到核质需要ATP。由于这种通透细胞模型简单有效,并且能有效地与外源性因素配合使用,它应该为研究核磷蛋白从核仁易位到核质的生化特征提供一个强大的工具。