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Orai1 is an Entotic Ca2+ Channel for Non-Apoptotic Cell Death, Entosis in Cancer Development.


ABSTRACT: Entosis is a non-apoptotic cell death process that forms characteristic cell-in-cell structures in cancers, killing invading cells. Intracellular Ca2+ dynamics are essential for cellular processes, including actomyosin contractility, migration, and autophagy. However, the significance of Ca2+ and Ca2+ channels participating in entosis is unclear. Here, it is shown that intracellular Ca2+ signaling regulates entosis via SEPTIN-Orai1-Ca2+ /CaM-MLCK-actomyosin axis. Intracellular Ca2+ oscillations in entotic cells show spatiotemporal variations during engulfment, mediated by Orai1 Ca2+ 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. Ca2+ 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 Ca2+ channel that provides essential Ca2+ signaling and sheds light on the molecular mechanism underlying entosis that involves SEPTIN filaments, Orai1, and MLCK.

SUBMITTER: Lee AR 

PROVIDER: S-EPMC10190626 | biostudies-literature | 2023 May

REPOSITORIES: biostudies-literature

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Orai1 is an Entotic Ca<sup>2+</sup> Channel for Non-Apoptotic Cell Death, Entosis in Cancer Development.

Lee Ah Reum AR   Park Chan Young CY  

Advanced science (Weinheim, Baden-Wurttemberg, Germany) 20230324 14


Entosis is a non-apoptotic cell death process that forms characteristic cell-in-cell structures in cancers, killing invading cells. Intracellular Ca<sup>2+</sup> dynamics are essential for cellular processes, including actomyosin contractility, migration, and autophagy. However, the significance of Ca<sup>2+</sup> and Ca<sup>2+</sup> channels participating in entosis is unclear. Here, it is shown that intracellular Ca<sup>2+</sup> signaling regulates entosis via SEPTIN-Orai1-Ca<sup>2+</sup> /CaM  ...[more]

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