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Published on: May 3, 2024
Different involvement of extracellular calcium in two modes of cell death induced by nanosecond pulsed electric
Keiko Morotomi-Yano1, Hidenori Akiyama2, Ken-ichi Yano1
1Department of Bioelectrics, Institute of Pulsed Power Science, Kumamoto University, Japan.
Abstract:
Exposure of cultured cells to nanosecond pulsed electric fields (nsPEFs) induces various cellular responses, including the influx of extracellular Ca2+ and cell death. Recently, nsPEFs have been regarded as a novel means of cancer therapy, but their molecular mechanism of action remains to be fully elucidated. Here, we demonstrate the involvement of extracellular Ca2+ in nsPEF-induced cell death. Extracellular Ca2+ was essential for necrosis and consequent poly(ADP-ribose) (PAR) formation in HeLa S3 cells. Treatment with a Ca2+ ionophore enhanced necrosis as well as PAR formation in nsPEF-exposed HeLa S3 cells. In the absence of extracellular Ca2+, HeLa S3 cells were less susceptible to nsPEFs and exhibited apoptotic proteolysis of caspase 3 and PARP-1. HeLa S3 cells retained the ability to undergo apoptosis even after nsPEF exposure but instead underwent necrosis, suggesting that necrosis is the preferential mode of cell death. In K562 and HEK293 cells, exposure to nsPEFs resulted in the formation of necrosis-associated PAR, whereas Jurkat cells exclusively underwent apoptosis independently of extracellular Ca2+. These observations demonstrate that the mode of cell death induced by nsPEFs is cell-type dependent and that extracellular Ca2+ is a critical factor for nsPEF-induced necrosis.
Insights
Nanosecond pulsed electric fields (nsPEFs) trigger cell death. Extracellular calcium is crucial for nsPEF-induced necrosis, a cell-death pathway preferred over apoptosis in many cell types.
Area of Science:
- Cell Biology
- Biophysics
Background:
- Nanosecond pulsed electric fields (nsPEFs) show promise for cancer therapy.
- The precise molecular mechanisms underlying nsPEF-induced cell death are not fully understood.
Purpose of the Study:
- To investigate the role of extracellular calcium (Ca2+) in nsPEF-induced cell death.
- To determine the preferred cell death pathway following nsPEF exposure.
Main Methods:
- Exposure of cultured cell lines (HeLa S3, K562, HEK293, Jurkat) to nsPEFs.
- Manipulation of extracellular Ca2+ levels using a Ca2+ ionophore.
- Analysis of cell death modes (necrosis, apoptosis) and associated molecular markers (PAR formation, caspase 3, PARP-1 cleavage).
Main Results:
- Extracellular Ca2+ is essential for nsPEF-induced necrosis and poly(ADP-ribose) (PAR) formation in HeLa S3 cells.
- In Ca2+-free conditions, HeLa S3 cells showed increased susceptibility to apoptosis rather than necrosis after nsPEF exposure.
- K562 and HEK293 cells exhibited necrosis-associated PAR formation upon nsPEF exposure, while Jurkat cells underwent apoptosis independently of extracellular Ca2+.
Conclusions:
- The mode of cell death induced by nsPEFs is cell-type dependent.
- Extracellular Ca2+ plays a critical role in promoting nsPEF-induced necrosis.
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