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Receptor-mediated control of regulatory volume decrease (RVD) and apoptotic volume decrease (AVD)

Authors

  • Yasunobu Okada,

    1. Department of Cell Physiology, National Institute for Physiological Sciences; and CREST, Japan Science and Technology Corporation, Okazaki 444-8585, Japan
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  • Emi Maeno,

    1. Department of Cell Physiology, National Institute for Physiological Sciences; and CREST, Japan Science and Technology Corporation, Okazaki 444-8585, Japan
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  • Takahiro Shimizu,

    1. Department of Cell Physiology, National Institute for Physiological Sciences; and CREST, Japan Science and Technology Corporation, Okazaki 444-8585, Japan
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  • Katsuya Dezaki,

    1. Department of Cell Physiology, National Institute for Physiological Sciences; and CREST, Japan Science and Technology Corporation, Okazaki 444-8585, Japan
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  • Jun Wang,

    1. Department of Cell Physiology, National Institute for Physiological Sciences; and CREST, Japan Science and Technology Corporation, Okazaki 444-8585, Japan
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  • Shigeru Morishima

    1. Department of Cell Physiology, National Institute for Physiological Sciences; and CREST, Japan Science and Technology Corporation, Okazaki 444-8585, Japan
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Corresponding author
Y. Okada: Department of Cell Physiology, National Institute for Physiological Sciences, Myodaiji-cho, Okazaki 444-8585, Japan.
Email: okada@nips.ac.jp

Abstract

A fundamental property of animal cells is the ability to regulate their own cell volume. Even under hypotonic stress imposed by either decreased extracellular or increased intracellular osmolarity, the cells can re-adjust their volume after transient osmotic swelling by a mechanism known as regulatory volume decrease (RVD). In most cell types, RVD is accomplished mainly by KCl efflux induced by parallel activation of K+ and Cl channels. We have studied the molecular mechanism of RVD in a human epithelial cell line (Intestine 407). Osmotic swelling results in a significant increase in the cytosolic Ca2+ concentration and thereby activates intermediate-conductance Ca2+-dependent K+ (IK) channels. Osmotic swelling also induces ATP release from the cells to the extracellular compartment. Released ATP stimulates purinergic ATP (P2Y2) receptors, thereby inducing phospholipase C-mediated Ca2+ mobilization. Thus, RVD is facilitated by stimulation of P2Y2 receptors due to augmentation of IK channels. In contrast, stimulation of another G protein-coupled Ca2+-sensing receptor (CaR) enhances the activity of volume-sensitive outwardly rectifying Cl channels, thereby facilitating RVD. Therefore, it is possible that Ca2+ efflux stimulated by swelling-induced and P2Y2 receptor-mediated intracellular Ca2+ mobilization activates the CaR, thereby secondarily upregulating the volume-regulatory Cl conductance. On the other hand, the initial process towards apoptotic cell death is coupled to normotonic cell shrinkage, called apoptotic volume decrease (AVD). Stimulation of death receptors, such as TNFα receptor and Fas, induces AVD and thereafter biochemical apoptotic events in human lymphoid (U937), human epithelial (HeLa), mouse neuroblastoma × rat glioma hybrid (NG108-15) and rat phaeochromocytoma (PC12) cells. In those cells exhibiting AVD, facilitation of RVD is always observed. Both AVD induction and RVD facilitation as well as succeeding apoptotic events can be abolished by prior treatment with a blocker of volume-regulatory K+ or Cl channels, suggesting that AVD is caused by normotonic activation of ion channels that are normally involved in RVD under hypotonic conditions. Therefore, it is likely that G protein-coupled receptors involved in RVD regulation and death receptors triggering AVD may share common downstream signals which should give us key clues to the detailed mechanisms of volume regulation and survival of animal cells. In this Topical Review, we look at the physiological ionic mechanisms of cell volume regulation and cell death-associated volume changes from the facet of receptor-mediated cellular processes.

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