electroendocytosis is driven by the binding of electrochemically produced protons to the cell’s surfaceelectroendocytosis是由绑定的电化学产生质子细胞的表面.pdfVIP
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electroendocytosis is driven by the binding of electrochemically produced protons to the cell’s surfaceelectroendocytosis是由绑定的电化学产生质子细胞的表面
Electroendocytosis Is Driven by the Binding of
Electrochemically Produced Protons to the Cell’s Surface
Nadav Ben-Dov, Inna Rozman Grinberg, Rafi Korenstein*
Department of Physiology and Pharmacology, Faculty of Medicine, Tel-Aviv University, Tel-Aviv, Israel
Abstract
Electroendocytosis involves the exposure of cells to pulsed low electric field and is emerging as a complementary method
to electroporation for the incorporation of macromolecules into cells. The present study explores the underlying mechanism
of electroendocytosis and its dependence on electrochemical byproducts formed at the electrode interface. Cell
suspensions were exposed to pulsed low electric field in a partitioned device where cells are spatially restricted relative to
the electrodes. The cellular uptake of dextran-FITC was analyzed by flow cytometery and visualized by confocal microscopy.
We first show that uptake occurs only in cells adjacent to the anode. The enhanced uptake near the anode is found to
depend on electric current density rather than on electric field strength, in the range of 5 to 65 V/cm. Electrochemically
produced oxidative species that impose intracellular oxidative stress, do not play any role in the stimulated uptake. An
inverse dependence is found between electrically induced uptake and the solution’s buffer capacity. Electroendocytosis can
be mimicked by chemically acidifying the extracellular solution which promotes the enhanced uptake of dextran polymers
and the uptake of plasmid DNA. Electrochemical production of protons at the anode interface is responsible for inducing
uptake of macromolecules into cells exposed to a pulsed low electric field. Expanding the understanding of the mechanism
involved in electric fields induced drug-delivery into cells, is expected to contribute to clinical therapy applications in the
fu
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