Department of Basic Sciences, UND School of Medicine and Health Sciences, 501 N Columbia Rd., Grand Forks, ND 58202-9037, USA.
Cell Signal. 2013 Nov;25(11):2125-35. doi: 10.1016/j.cellsig.2013.07.004. Epub 2013 Jul 6.
A-Kinase Anchoring Proteins (AKAPs) direct the flow of cellular information by positioning multiprotein signaling complexes into proximity with effector proteins. However, certain AKAPs are not stationary but can undergo spatiotemporal redistribution in response to stimuli. Gravin, a 300kD AKAP that intersects with a diverse signaling array, is localized to the plasma membrane but has been shown to translocate to the cytosol following the elevation of intracellular calcium ([Ca(2+)]i). Despite the potential for gravin redistribution to impact multiple signaling pathways, the dynamics of this event remain poorly understood. In this study, quantitative microscopy of cells expressing gravin-EGFP revealed that Ca(2+) elevation caused the complete translocation of gravin from the cell cortex to the cytosol in as little as 60s of treatment with ionomycin or thapsigargin. In addition, receptor mediated signaling was also shown to cause gravin redistribution following ATP treatment, and this event required both [Ca(2+)]i elevation and PKC activation. To understand the mechanism for Ca(2+) mediated gravin dynamics, deletion of calmodulin-binding domains revealed that a fourth putative calmodulin binding domain called CB4 (a.a. 670-694) is critical for targeting gravin to the cell cortex despite its location downstream of gravin's membrane-targeting domains, which include an N-terminal myristoylation site and three polybasic domains. Finally, confocal microscopy of cells co-transfected with gravin-EYFP and PKA RII-ECFP revealed that gravin redistribution mediated by ionomycin, thapsigargin, and ATP each triggered the gravin-dependent loss of PKA localized at the cell cortex. Our results support the hypothesis that gravin redistribution regulates cross-talk between PKA-dependent signaling and receptor-mediated events involving Ca(2+) and PKC.
A-激酶锚定蛋白(AKAPs)通过将多蛋白信号复合物定位在与效应蛋白接近的位置来指导细胞信息的流动。然而,某些 AKAP 并不是固定的,而是可以响应刺激进行时空重新分布。Gravin 是一种 300kD 的 AKAP,与多种信号阵列相交,定位于质膜,但已被证明在细胞内钙升高([Ca(2+)]i)后向细胞质易位。尽管 Gravin 重新分布可能会影响多种信号通路,但这一事件的动态仍知之甚少。在这项研究中,通过对表达 Gravin-EGFP 的细胞进行定量显微镜检查,发现钙升高导致 Gravin 在离子霉素或 thapsigargin 处理 60 秒内完全从细胞皮层易位到细胞质。此外,受体介导的信号转导也被证明会导致 ATP 处理后 Gravin 重新分布,这一事件需要[Ca(2+)]i 升高和 PKC 激活。为了了解 Ca(2+)介导的 Gravin 动力学的机制,钙调蛋白结合域的缺失表明,第四个假定的钙调蛋白结合域 CB4(氨基酸 670-694)对于将 Gravin 靶向细胞皮层至关重要,尽管它位于 Gravin 的膜靶向结构域下游,这些结构域包括一个 N 端豆蔻酰化位点和三个多碱性结构域。最后,对共转染 Gravin-EYFP 和 PKA RII-ECFP 的细胞进行共聚焦显微镜检查表明,离子霉素、thapsigargin 和 ATP 介导的 Gravin 重新分布都触发了依赖 Gravin 的 PKA 在细胞皮层的丢失。我们的结果支持这样一种假设,即 Gravin 重新分布调节 PKA 依赖性信号和涉及 Ca(2+)和 PKC 的受体介导事件之间的串扰。