Liu T F, Johnson R G
National Laboratory of Biomembrane and Biotechnology, College of Life Sciences, Peking University, Beijing, China.
Methods Find Exp Clin Pharmacol. 1999 Jul-Aug;21(6):387-90. doi: 10.1358/mf.1999.21.6.541917.
In order to investigate the site of active phosphorylation under treatment with TPA, both wild type (WT) fibroblasts and fibroblasts from Cx43-knockout mice transfected with Cx43 mutated at ser368 were used to study the effects of TPA on dye leakage and gap junction assembly. Results showed that in control conditions with or without EGTA, no significant differences in dye leakage were observed between these two kinds of cells. However, under TPA treatment, non-leakage cases in the mutant cells were much less than those in WT cells. In the two types of reaggregated cells, there was a marked difference in the capacity for dye transfer. Dye transfer in WT cells was 4-fold stronger than in mutant cells. While under TPA treatment, the difference between WT and mutant cells was diminished suggesting that ser368 was probably the most important phosphorylation site under treatment with TPA.
为了研究佛波酯(TPA)处理下的活性磷酸化位点,野生型(WT)成纤维细胞和转染了ser368位点突变的Cx43的Cx43基因敲除小鼠的成纤维细胞被用于研究TPA对染料泄漏和间隙连接组装的影响。结果显示,在有或没有乙二醇双乙醚二胺四乙酸(EGTA)的对照条件下,这两种细胞之间在染料泄漏方面未观察到显著差异。然而,在TPA处理下,突变细胞中的非泄漏情况比WT细胞中的少得多。在两种重新聚集的细胞类型中,染料转移能力存在显著差异。WT细胞中的染料转移比突变细胞强4倍。而在TPA处理下,WT和突变细胞之间的差异减小,这表明ser368可能是TPA处理下最重要的磷酸化位点。