Laboratory of Cell Signaling, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo 113-0033, Japan.
Laboratory of Cell Signaling, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo 113-0033, Japan.
Cell Rep. 2018 Mar 13;22(11):2809-2817. doi: 10.1016/j.celrep.2018.02.045.
Cell volume regulation is a vital system for cellular activities. When perturbed by hypoosmotic or hyperosmotic stress, cells immediately induce the cell volume recovery system, regulatory volume decrease (RVD) or regulatory volume increase (RVI), respectively. In contrast to the knowledge about effector molecules, the molecular mechanisms linking osmosensing to RVD/RVI induction remain unknown. Additionally, few reciprocal responders in the bidirectional osmotic stress response have been identified. We previously reported that ASK3 bidirectionally switches its kinase activity under osmotic stress. Herein we demonstrate that ASK3 controls both RVD and RVI under osmotic stress. Using a high-content genome-wide small interfering RNA (siRNA) screen, we identify PP6 as a direct ASK3 inactivator. Furthermore, PP6 rapidly interacts with ASK3 in an osmolality-dependent manner, and it inactivates ASK3 to induce RVI and, thereby, cell survival under hyperosmotic stress. These findings suggest that the PP6-ASK3 interaction is a core module in the bidirectional osmotic stress response.
细胞体积调节是细胞活动的重要系统。当受到低渗或高渗应激的干扰时,细胞会立即分别诱导细胞体积恢复系统,即调节性体积减少(RVD)或调节性体积增加(RVI)。与效应分子的知识相比,将渗透压感应与 RVD/RVI 诱导联系起来的分子机制仍然未知。此外,在双向渗透胁迫反应中很少有相互的应答者被识别。我们之前报道过,ASK3 在渗透胁迫下双向切换其激酶活性。本文中我们证明了 ASK3 在渗透胁迫下控制 RVD 和 RVI。通过使用高内涵全基因组小干扰 RNA(siRNA)筛选,我们鉴定出 PP6 是 ASK3 的直接失活剂。此外,PP6 以渗透压依赖性的方式与 ASK3 快速相互作用,并使其失活以诱导 RVI,从而在高渗胁迫下促进细胞存活。这些发现表明,PP6-ASK3 相互作用是双向渗透应激反应的核心模块。