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February 12, 2026International Journal of Molecular Sciences0 citationsOpen Access

High Activity of Hemichannels Permeable to Calcium Ions Leads to ROS Generation and Reduced Cell Viability

WVWalter VásquezCUCarolina Andrea UrrutiaXLXimena López

Key Points

  • The aim is to determine how high hemichannel activity contributes to calcium influx and cell death in specific cell types.
  • Used HeLa cells expressing Cx39, Cx43, Cx45, or Panx1 and parental control cells
  • Exposed cells to an alkaline solution (pH 8.5) to stimulate hemichannel activity
  • Performed dye uptake assays to measure hemichannel activity and calcium influx
  • High hemichannel activity was observed in all transfected cells, but not in parental control cells
  • Cx45 was identified as a novel calcium-permeable hemichannel
  • Alkaline stress increased cytosolic calcium levels, leading to oxidative stress and reduced cell viability

Abstract

Connexins (Cxs) and pannexin1 (Panx1) form hemichannels (HCs) that enable the exchange of ions and small molecules between the intracellular and extracellular compartments. Since an elevated cytoplasmic Ca2+ concentration promotes cell death and elevated HC activity has been implicated in pathological conditions, we investigated whether high HC activity contributes to Ca2+ influx and cell death. HeLa parental cells and HeLa cells expressing Cx39, Cx43, Cx45, or Panx1 were exposed to an alkaline extracellular solution (pH 8.5) to increase HC activity. Under these conditions, dye uptake assays revealed high HC activity in all transfected cells but not in parental control cells. Previous studies have shown that Cx43 HCs, but not Cx39 and Panx1 HCs, allow the influx of extracellular Ca2+. Here, we also found that exposure of Cx45 transfectants to pH 8.5 activated HCs and allowed the influx of extracellular Ca2+. Only in cells expressing functional HCs permeable to Ca2+ did the elevated HC activity heighten the cytosolic Ca2+ concentration, which promoted lipid peroxidation and reduced cell viability. The effects were also abolished by the removal of extracellular divalent cations, suggesting that a Ca2+ influx that triggers downstream deleterious effects is required. Our findings identify Cx45 as a novel Ca2+-permeable HC, and they reveal that alkaline stress promotes Ca2+ entry via Cx43 and Cx45 HCs, which in turn leads to oxidative stress and cell death.

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Cite This Study

Vásquez et al. (2026) studied this question.

synapsesocial.com/papers/698d6de45be6419ac0d5324chttps://doi.org/10.3390/ijms27041699
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