Department of Biological Sciences, Ulsan National Institute of Science and Technology, Ulsan, 44919, Republic of Korea.
Adv Sci (Weinh). 2023 May;10(14):e2205913. doi: 10.1002/advs.202205913. Epub 2023 Mar 24.
Entosis is a non-apoptotic cell death process that forms characteristic cell-in-cell structures in cancers, killing invading cells. Intracellular Ca dynamics are essential for cellular processes, including actomyosin contractility, migration, and autophagy. However, the significance of Ca and Ca channels participating in entosis is unclear. Here, it is shown that intracellular Ca signaling regulates entosis via SEPTIN-Orai1-Ca /CaM-MLCK-actomyosin axis. Intracellular Ca oscillations in entotic cells show spatiotemporal variations during engulfment, mediated by Orai1 Ca channels in plasma membranes. SEPTIN controlled polarized distribution of Orai1 for local MLCK activation, resulting in MLC phosphorylation and actomyosin contraction, leads to internalization of invasive cells. Ca chelators and SEPTIN, Orai1, and MLCK inhibitors suppress entosis. This study identifies potential targets for treating entosis-associated tumors, showing that Orai1 is an entotic Ca channel that provides essential Ca signaling and sheds light on the molecular mechanism underlying entosis that involves SEPTIN filaments, Orai1, and MLCK.
细胞侵入是一种非细胞凋亡的死亡过程,会在癌症中形成特征性的“细胞吃细胞”结构,从而杀死入侵的细胞。细胞内钙离子动力学对于包括肌动球蛋白收缩、迁移和自噬在内的细胞过程至关重要。然而,参与细胞侵入的钙离子和钙通道的意义尚不清楚。本研究表明,细胞内钙离子信号通过 SEPTIN-Orai1-Ca/CaM-MLCK-肌动球蛋白轴来调节细胞侵入。侵入细胞的细胞内钙离子振荡在吞噬过程中表现出时空变化,这是由质膜中的 Orai1 钙离子通道介导的。SEPTIN 控制 Orai1 的极化分布,以局部激活 MLCK,导致 MLC 磷酸化和肌动球蛋白收缩,从而使入侵细胞内化。钙离子螯合剂和 SEPTIN、Orai1 和 MLCK 抑制剂抑制细胞侵入。这项研究确定了治疗与细胞侵入相关的肿瘤的潜在靶点,表明 Orai1 是一种侵入性钙通道,提供了必要的钙信号,并揭示了涉及 SEPTIN 纤维、Orai1 和 MLCK 的细胞侵入的分子机制。