Department of Chemistry, Korea Advanced Institute of Science and Technology, Daejeon, South Korea.
Biochem Biophys Res Commun. 2013 Apr 26;434(1):8-14. doi: 10.1016/j.bbrc.2013.03.082. Epub 2013 Apr 6.
Binding of Gas6 to Axl (Gas6/Axl axis) alters cellular functions, including migration, invasion, proliferation, and survival. However, the molecular mechanisms underlying Gas6-mediated cell migration remain poorly understood. In this study, we found that Gas6 induced the activation of JNK and ERK1/2 signaling in cancer cells expressing Axl, resulting in the phosphorylation of activator protein-1 (AP-1) transcription factors c-Jun and ATF-2, and induction of Slug. Depletion of c-Jun or ATF-2 by siRNA attenuated the Gas6-induced expression of Slug. Slug expression was required for cell migration and E-cadherin reduction/vimentin induction induced by Gas6. These results suggest that Gas6 induced cell migration via Slug upregulation in JNK- and ERK1/2-dependent mechanisms. These data provide an important insight into the molecular mechanisms mediating Gas6-induced cell migration.
Gas6 与 Axl 的结合(Gas6/Axl 轴)改变了细胞功能,包括迁移、侵袭、增殖和存活。然而,Gas6 介导的细胞迁移的分子机制仍知之甚少。在这项研究中,我们发现 Gas6 诱导表达 Axl 的癌细胞中 JNK 和 ERK1/2 信号的激活,导致激活蛋白-1 (AP-1) 转录因子 c-Jun 和 ATF-2 的磷酸化,并诱导 Slug 的表达。siRNA 敲低 c-Jun 或 ATF-2 可减弱 Gas6 诱导的 Slug 表达。Gas6 诱导的细胞迁移和 E-钙黏蛋白减少/波形蛋白诱导需要 Slug。这些结果表明,Gas6 通过 JNK 和 ERK1/2 依赖性机制诱导 Slug 上调来诱导细胞迁移。这些数据为 Gas6 诱导的细胞迁移的分子机制提供了重要的见解。