Okada Yasunobu, Numata Tomohiro, Sabirov Ravshan Z, Kashio Makiko, Merzlyak Peter G, Sato-Numata Kaori
National Institute for Physiological Sciences (NIPS), Okazaki, Japan.
Department of Integrative Physiology, Graduate School of Medicine, AkitaUniversity, Akita, Japan.
Front Cell Dev Biol. 2023 Sep 29;11:1246955. doi: 10.3389/fcell.2023.1246955. eCollection 2023.
Cell volume regulation (CVR) is a prerequisite for animal cells to survive and fulfill their functions. CVR dysfunction is essentially involved in the induction of cell death. In fact, sustained normotonic cell swelling and shrinkage are associated with necrosis and apoptosis, and thus called the necrotic volume increase (NVI) and the apoptotic volume decrease (AVD), respectively. Since a number of ubiquitously expressed ion channels are involved in the CVR processes, these volume-regulatory ion channels are also implicated in the NVI and AVD events. In Part 1 and Part 2 of this series of review articles, we described the roles of swelling-activated anion channels called VSOR or VRAC and acid-activated anion channels called ASOR or PAC in CVR and cell death processes. Here, Part 3 focuses on therein roles of Ca-permeable non-selective TRPM2 and TRPM7 cation channels activated by stress. First, we summarize their phenotypic properties and molecular structure. Second, we describe their roles in CVR. Since cell death induction is tightly coupled to dysfunction of CVR, third, we focus on their participation in the induction of or protection against cell death under oxidative, acidotoxic, excitotoxic, and ischemic conditions. In this regard, we pay attention to the sensitivity of TRPM2 and TRPM7 to a variety of stress as well as to their capability to physicall and functionally interact with other volume-related channels and membrane enzymes. Also, we summarize a large number of reports hitherto published in which TRPM2 and TRPM7 channels are shown to be involved in cell death associated with a variety of diseases or disorders, in some cases as double-edged swords. Lastly, we attempt to describe how TRPM2 and TRPM7 are organized in the ionic mechanisms leading to cell death induction and protection.
细胞体积调节(CVR)是动物细胞存活并履行其功能的先决条件。CVR功能障碍本质上与细胞死亡的诱导有关。事实上,持续性等渗性细胞肿胀和收缩分别与坏死和凋亡相关,因此分别称为坏死性体积增加(NVI)和凋亡性体积减少(AVD)。由于许多普遍表达的离子通道参与CVR过程,这些体积调节离子通道也与NVI和AVD事件有关。在本系列综述文章的第1部分和第2部分中,我们描述了称为VSOR或VRAC的肿胀激活阴离子通道以及称为ASOR或PAC的酸激活阴离子通道在CVR和细胞死亡过程中的作用。在这里,第3部分重点关注应激激活的钙通透性非选择性TRPM2和TRPM7阳离子通道在其中的作用。首先,我们总结它们的表型特性和分子结构。其次,我们描述它们在CVR中的作用。由于细胞死亡诱导与CVR功能障碍紧密相关,第三,我们重点关注它们在氧化、酸毒性、兴奋性毒性和缺血条件下参与细胞死亡的诱导或保护作用。在这方面,我们关注TRPM2和TRPM7对各种应激的敏感性以及它们与其他体积相关通道和膜酶进行物理和功能相互作用的能力。此外,我们总结了迄今为止发表的大量报告,其中TRPM2和TRPM7通道被证明与多种疾病或病症相关的细胞死亡有关,在某些情况下是双刃剑。最后,我们试图描述TRPM2和TRPM7在导致细胞死亡诱导和保护的离子机制中是如何组织的。