Scheidl H, Chandra T, Gmeiner B, Zerlauth G, Scita G, Wolf G
Department of Nutritional Sciences, University of California, Berkeley 94720.
Carcinogenesis. 1991 Oct;12(10):1791-4. doi: 10.1093/carcin/12.10.1791.
Previous work from our laboratory showed that tumor promoters such as phorbol ester (TPA) stimulated the release of fibronectin (FN) from the surface of several cell types in culture, and that this stimulation was counteracted by retinoic acid. Diacylglycerols (DAGs) are the endogenous ligands of the TPA receptor and can activate and translocate protein kinase C (PKC) in a manner similar to TPA. To show that the release of FN is related to activation of PKC, we tested the action of DAGs on FN release from human lung fibroblasts and its counteraction by retinoic acid. We found that DAGs stimulated the release of FN in a concentration- and time-dependent manner. The stimulation of the release of FN correlated with the translocation-activation of PKC by DAG. Retinoic acid reversed the action of DAG with respect to stimulation of FN release and inhibited this release even in the absence of DAG. These results suggest that the release of FN is in some way related to translocation-activation of PKC.
我们实验室之前的研究表明,诸如佛波酯(TPA)之类的肿瘤启动子可刺激培养中的几种细胞类型表面释放纤连蛋白(FN),而视黄酸可抵消这种刺激作用。二酰基甘油(DAGs)是TPA受体的内源性配体,能够以类似于TPA的方式激活并转位蛋白激酶C(PKC)。为了证明FN的释放与PKC的激活有关,我们测试了DAGs对人肺成纤维细胞释放FN的作用以及视黄酸对其的抵消作用。我们发现,DAGs以浓度和时间依赖性方式刺激FN的释放。FN释放的刺激与DAG对PKC的转位激活相关。视黄酸可逆转DAG对FN释放的刺激作用,并且即使在没有DAG的情况下也能抑制这种释放。这些结果表明,FN的释放与PKC的转位激活在某种程度上相关。