Illinger D, Italiano L, Beck J P, Waltzinger C, Kuhry J G
Laboratoire de Biophysique, URA 491 du CNRS, Strasbourg, France.
Biol Cell. 1993;79(3):265-8. doi: 10.1016/0248-4900(93)90146-6.
1-[4-(trimethylamino)phenyl]-6-phenylhexa-1,3,5-triene (TMA-DPH), a membrane fluorescence probe, interacts with living cells by instantaneous partition between the external medium and the plasma membrane, where it becomes fluorescent. The corresponding fluorescence intensity is then proportional to the cell surface. On the other hand, once incorporated into the plasma membrane, TMA-DPH follows this membrane in the constitutive intracellular traffic and behaves as a monitor for endocytosis. Using this tool on L929 synchronized cells, we showed that the endocytosis levels after 30 min uptake of the probe increased from G1 to mitosis, when they abruptly decreased. The cell surface remained constant throughout the cell cycle, except at the beginning of mitosis when it almost doubled.
1-[4-(三甲基氨基)苯基]-6-苯基-1,3,5-己三烯(TMA-DPH)是一种膜荧光探针,它通过在外部介质和质膜之间的瞬间分配与活细胞相互作用,并在质膜处发出荧光。相应的荧光强度随后与细胞表面成正比。另一方面,一旦TMA-DPH掺入质膜,它就会在组成型细胞内运输过程中跟随该膜移动,并作为内吞作用的监测器。在L929同步化细胞上使用该工具,我们发现,在摄取探针30分钟后,内吞水平从G1期到有丝分裂期增加,然后在有丝分裂期突然下降。除了在有丝分裂开始时细胞表面几乎翻倍外,在整个细胞周期中细胞表面保持恒定。