Bachmann M, Zaubitzer T, Müller W E
Institut für Physiologische Chemie, Johannes-Gutenberg Universität, Mainz, Germany.
Exp Cell Res. 1992 Aug;201(2):387-98. doi: 10.1016/0014-4827(92)90288-j.
The nuclear autoantigen La, a transcription/termination factor of RNA polymerase III, was recently shown to translocalize to the cell surface of growth-stimulated cells during transition from G0- to G1-phase. Here we describe the staining of living mitotic cells with the anti-La mab La11G7. Moreover, La protein added to cell culture medium was able to enter into synchronized mitotic cells. Uptake was inhibited by the anti-La mab. La protein taken up into prophase cells assembled into a fibrillar network. Taken up byu ana/telophase cells, La protein was preferentially transported into the newly forming or formed nuclei. This import allowed us to study directly the intranuclear localization of La protein in living cells by the use confocal laser scanning microscopy (cLSM). Adsorbed La protein was found in the nucleoplasm but also assembled into nuclear speckles. Some of these speckles surrounded the nucleolus like a ring.
核自身抗原La是RNA聚合酶III的转录/终止因子,最近研究表明,在从G0期向G1期转变过程中,生长刺激细胞的La会转位至细胞表面。在此,我们描述了用抗La单克隆抗体La11G7对活有丝分裂细胞进行染色的情况。此外,添加到细胞培养基中的La蛋白能够进入同步化的有丝分裂细胞。这种摄取被抗La单克隆抗体所抑制。摄取到前期细胞中的La蛋白组装成纤维状网络。被末期/终末期细胞摄取后,La蛋白优先转运至新形成或已形成的细胞核中。这种导入使我们能够通过共聚焦激光扫描显微镜(cLSM)直接研究活细胞中La蛋白的核内定位。发现吸附的La蛋白存在于核质中,也会组装成核斑。其中一些核斑像环一样围绕着核仁。