• DocumentCode
    752420
  • Title

    Nanosecond pulsed electric field (nsPEF) effects on cells and tissues: apoptosis induction and tumor growth inhibition

  • Author

    Beebe, Stephen J. ; Fox, P.M. ; Rec, L.J. ; Somers, K. ; Stark, Robert H. ; Schoenbach, Karl H.

  • Author_Institution
    Dept. of Pediatrics, Eastern Virginia Med. Sch., Norfolk, VA, USA
  • Volume
    30
  • Issue
    1
  • fYear
    2002
  • fDate
    2/1/2002 12:00:00 AM
  • Firstpage
    286
  • Lastpage
    292
  • 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; cellular biophysics; electric field effects; patient treatment; pulsed power supplies; tumours; Annexin-V-FITC binding; HL-60 cells; Jurkat cells; Mouse fibrosarcoma tumors; amelioration; apoptosis; apoptosis induction; biofouling; caspase activation; cell shrinkage; cells; cultured cells; decontamination; electric field intensity-dependent effects; electric field interactions; electroporation pulses; energy density; energy density independent effects; flow cytometry; fluorescent markers; fragmented DNA; functional changes; high intensity nanosecond pulsed electric field effects; human cells; immunofluorescence microscopy; intact cells; mice; phosphatidylserine; programmed cell. death; pulse duration; pulse duration-dependent effects; pulse power technology; reduced tumor growth; structural changes; temperature-independent effects; tissues; tumor growth inhibition; Cells (biology); Decontamination; Humans; Immune system; Mice; Microscopy; Neoplasms; Plasma density; Plasma temperature; Solids;
  • fLanguage
    English
  • Journal_Title
    Plasma Science, IEEE Transactions on
  • Publisher
    ieee
  • ISSN
    0093-3813
  • Type

    jour

  • DOI
    10.1109/TPS.2002.1003872
  • Filename
    1003872