Abstract

Cell volume regulation (CVR) is essential for survival and functions of animal cells. Actually, normotonic cell shrinkage and swelling are coupled to apoptotic and necrotic cell death and thus called the apoptotic volume decrease (AVD) and the necrotic volume increase (NVI), respectively. A number of ubiquitously expressed anion and cation channels are involved not only in CVD but also in cell death induction. This series of review articles address the question how cell death is induced or protected with using ubiquitously expressed ion channels such as swelling-activated anion channels, acid-activated anion channels and several types of TRP cation channels including TRPM2 and TRPM7. The Part 1 focuses on the roles of the volume-sensitive outwardly rectifying anion channels (VSOR), also called the volume-regulated anion channel (VRAC), which is activated by cell swelling or reactive oxygen species (ROS) in a manner dependent on intracellular ATP. First we describe phenotypical properties, the molecular identity, and physical pore dimensions of VSOR/VRAC. Second, we highlight the roles of VSOR/VRAC in the release of organic signaling molecules, such as glutamate, glutathione, ATP and cGAMP, that play roles as double-edged swords in cell survival. Third, we discuss how VSOR/VRAC is involved in CVR and cell volume dysregulation as well as in the induction of or protection from apoptosis, necrosis and regulated necrosis under pathophysiological conditions.

Highlights

  • For the survival of animal cells, control of their cell volume is essential, since the water permeability of cell membranes is high enough to allow passive water fluxes in response to changes in the extracellular and/or intracellular osmolarity under both physiological and pathological situations

  • We demonstrated that volume-sensitive outwardly rectifying anion channels (VSOR) activity is involved in induction of apoptotic volume decrease (AVD) and apoptosis in human cancer KB cells stimulated with cisplatin (Ise et al, 2005)

  • Since astrocytic VSOR is activated by adenosine triphosphate (ATP) (Akita et al, 2011) and glutamate (Akita and Okada, 2014) through stimulation of their G protein-coupled receptor (GPCR) via a signal here called Ca2+·reactive oxygen species (ROS) which represents ROS production mediated by Ca2+ nanodomains, glutamate release may be induced from astrocytes exposed to extracellular ATP and glutamate

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Summary

Introduction

For the survival of animal cells, control of their cell volume is essential, since the water permeability of cell membranes is high enough to allow passive water fluxes in response to changes in the extracellular and/or intracellular osmolarity under both physiological and pathological situations (see Books: Okada, 1998; Lang, 2006). ROLES OF VSOR/VRAC IN RELEASE OF ORGANIC SIGNALS FOR CELL DEATH INDUCTION/PROTECTION Note that this channel does not contribute to the bradykinin-induced glutamate release, which is solely mediated by VSOR activated by ROS and a Ca2+ nanodomain-related mechanism in astrocytes (Liu et al, 2009; Akita and Okada, 2011, 2014).

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