Biomedical Sciences Division, School of Medicine, University of California Riverside, Riverside, California, USA.
Prog Mol Biol Transl Sci. 2013;118:205-22. doi: 10.1016/B978-0-12-394440-5.00008-5.
Arrestins have emerged as important regulators of actin reorganization and cell migration. Both in their classical roles as mediators of receptor desensitization and internalization, and in their newer role as signaling scaffolds, β-arrestins help orchestrate the cellular response to chemotactic signals. However, there is still a considerable amount to be learned about the precise molecular mechanisms underlying these processes. This review discusses how, by regulating receptor internalization and by scaffolding of signaling molecules in discrete cellular locations, arrestins facilitate gradient sensing and cytoskeletal reorganization, ultimately resulting in cell migration. In addition, putative new targets of β-arrestin regulation that may play important roles in cell migration are discussed, as continued research on these targets may provide important details to fill in the current gaps in our understanding of these processes.
arrestins 已成为调节肌动蛋白重组和细胞迁移的重要调控因子。β-arrestin 在作为受体脱敏和内化的介质的经典作用以及作为信号支架的新作用中,帮助协调细胞对趋化信号的反应。然而,对于这些过程背后的精确分子机制,仍有许多需要了解。这篇综述讨论了 arrestins 如何通过调节受体内化以及在离散的细胞位置支架信号分子,促进梯度感应和细胞骨架重组,最终导致细胞迁移。此外,还讨论了β-arrestin 调节的可能新靶点,这些靶点可能在细胞迁移中发挥重要作用,因为对这些靶点的持续研究可能为填补我们对这些过程理解中的当前空白提供重要细节。