DocumentCode
1589078
Title
Nanosecond pulsed electric field (nsPEF) effects on cells and tissues: apoptosis induction and tumor growth inhibition
Author
Beebe, S.J. ; Fox, P.M. ; Rec, L.J. ; Somers, K. ; Stark, R.H. ; Schoenbach, K.H.
Author_Institution
Dept. of Pediatrics, Eastern Virginia Med. Sch., Norfolk, VA, USA
Volume
1
fYear
2001
Firstpage
211
Abstract
Pulse power technology using high intensity (up to 300 kV/cm) nanosecond pulsed electric fields (nsPEF) has been applied for decontamination and amelioration of biofouling, but until now effects on human cells have not been investigated. To analyze structural and functional changes in human cells and solid tumors following exposure to nsPEF we utilized flow cytometry and immunofluorescence microscopy. We provide further support for the hypothesis that as the pulse duration is decreased, there is a lower incidence of electric field interactions at the plasma membrane and a higher incidence of interactions with intracellular structures. The nsPEF effects are pulse duration/electric field intensity-dependent and energy density- or temperature-independent. We also show that nsPEF induces programmed cell death (apoptosis) in cultured cells as indicated by cell shrinkage, Annexin-V-FITC binding to phosphatidylserine on intact cells, and caspase activation. Mouse fibrosarcoma tumors exposed to nsPEF exhibit fragmented DNA and reduced tumor growth in a mouse model. These studies show that nsPEF effects are distinctly different than electroporation pulses and provide the first evidence for the potential application of nsPEF to induce apoptosis and inhibit tumor growth.
Keywords
bioelectric phenomena; biological effects of fields; biological tissues; cellular effects of radiation; electric field effects; tumours; apoptosis induction; caspase activation; cell shrinkage; electroporation pulses; flow cytometry; fragmented DNA; human cells; immunofluorescence microscopy; intact cells; intracellular structures; mouse fibrosarcoma tumors; mouse model; nanosecond pulsed electric field effects; phosphatidylserine; plasma membrane; programmed cell death; pulse duration; pulse power technology; reduced tumor growth; solid tumors; tumor growth inhibition; Cells (biology); Decontamination; Humans; Immune system; Mice; Microscopy; Neoplasms; Plasma density; Plasma temperature; Solids;
fLanguage
English
Publisher
ieee
Conference_Titel
Pulsed Power Plasma Science, 2001. PPPS-2001. Digest of Technical Papers
Conference_Location
Las Vegas, NV, USA
Print_ISBN
0-7803-7120-8
Type
conf
DOI
10.1109/PPPS.2001.1002030
Filename
1002030
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