Department of General Surgery, Qilu Hospital, Shandong University, Jinan 250012, Shandong, PR China.
Cancer Lett. 2011 Dec 1;311(1):38-47. doi: 10.1016/j.canlet.2011.06.025. Epub 2011 Jun 24.
Recently published studies have suggested that integrin trafficking is necessary to support cell migration, but the role of internalization and recycling of integrin αvβ6 in colon cancer cells remained unclear. In our study, we demonstrated the existence of the integrin cycle and found that inhibition of ERK2 phosphorylation by PD98059 or deletion of the ERK2 direct binding site on the β6 cytoplasmic domain could interrupt the internalization of integrin αvβ6, but had no effect on its recycling. Furthermore, integrin αvβ6 trafficking played a key role in the migration of colon cancer cells towards fibronectin. Activation of PKC significantly accelerated the internalization and recycling of integrin αvβ6, which could facilitate rapid redistribution of integrin αvβ6 and increase cell motility. When colon cancer cells became crowded, the increase in αvβ6 levels at the cell surface was not accompanied by a change in total αvβ6 expression in cell lysates. This change may be due to a redistribution of αvβ6 in cell microstructures and a rapid cellular response towards the demands of migration.
最近发表的研究表明,整合素运输对于支持细胞迁移是必要的,但整合素αvβ6在结肠癌细胞中的内化和回收的作用仍不清楚。在我们的研究中,我们证明了整合素循环的存在,并发现 ERK2 磷酸化的抑制(通过 PD98059)或 ERK2 直接结合β6 胞质域上的位点的缺失可以中断整合素αvβ6的内化,但对其回收没有影响。此外,整合素αvβ6的运输在结肠癌细胞向纤维连接蛋白的迁移中起着关键作用。PKC 的激活显著加速了整合素αvβ6的内化和回收,这可以促进整合素αvβ6的快速重新分布,并增加细胞迁移能力。当结肠癌细胞变得拥挤时,细胞表面αvβ6水平的增加并没有伴随着细胞裂解物中总αvβ6表达的变化。这种变化可能是由于细胞微结构中αvβ6的重新分布以及细胞对迁移需求的快速反应。