1 March 2006 Fluorescence microscopy imaging of electroperturbation in mammalian cells
Author Affiliations +
J. of Biomedical Optics, 11(2), 024010 (2006). doi:10.1117/1.2187970
Abstract
We report the design, integration, and validation of a fluorescence microscopy system for imaging of electroperturbation—the effects of nanosecond, megavolt-per-meter pulsed electric fields on biological cells and tissues. Such effects have potential applications in cancer therapy, gene regulation, and biophysical research by noninvasively disrupting intracellular compartments and inducing apoptosis in malignant cells. As the primary observing platform, an epifluorescence microscope integrating a nanosecond high-voltage pulser and a micrometer electrode chamber enable in situ imaging of the intracellular processes triggered by high electric fields. Using specific fluorescence molecular probes, the dynamic biological responses of Jurkat T lymphocytes to nanosecond electric pulses (nanoelectropulses) are studied with this system, including calcium bursts, the polarized translocation of phosphatidylserine (PS), and nuclear enlargement and chromatin/DNA structural changes.
Yinghua Sun, P. Thomas Vernier, Matthew Behrend, Jingjing Wang, Mya Mya Thu, Martin A. Gundersen, Laura Marcu, "Fluorescence microscopy imaging of electroperturbation in mammalian cells," Journal of Biomedical Optics 11(2), 024010 (1 March 2006). http://dx.doi.org/10.1117/1.2187970
JOURNAL ARTICLE
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KEYWORDS
Luminescence

Calcium

Microscopy

Imaging systems

Picosecond phenomena

Fermium

Frequency modulation

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