Literature DB >> 23692638

Light sources and cameras for standard in vitro membrane potential and high-speed ion imaging.

R Davies1, J Graham, M Canepari.   

Abstract

Membrane potential and fast ion imaging are now standard optical techniques routinely used to record dynamic physiological signals in several preparations in vitro. Although detailed resolution of optical signals can be improved by confocal or two-photon microscopy, high spatial and temporal resolution can be obtained using conventional microscopy and affordable light sources and cameras. Thus, standard wide-field imaging methods are still the most common in research laboratories and can often produce measurements with a signal-to-noise ratio that is superior to other optical approaches. This paper seeks to review the most important instrumentation used in these experiments, with particular reference to recent technological advances. We analyse in detail the optical constraints dictating the type of signals that are obtained with voltage and ion imaging and we discuss how to use this information to choose the optimal apparatus. Then, we discuss the available light sources with specific attention to light emitting diodes and solid state lasers. We then address the current state-of-the-art of available charge coupled device, electron multiplying charge coupled device and complementary metal oxide semiconductor cameras and we analyse the characteristics that need to be taken into account for the choice of optimal detector. Finally, we conclude by discussing prospective future developments that are likely to further improve the quality of the signals expanding the capability of the techniques and opening the gate to novel applications.
© 2013 The Authors Journal of Microscopy © 2013 Royal Microscopical Society.

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Year:  2013        PMID: 23692638     DOI: 10.1111/jmi.12047

Source DB:  PubMed          Journal:  J Microsc        ISSN: 0022-2720            Impact factor:   1.758


  4 in total

1.  Using simultaneous voltage and calcium imaging to study fast Ca(2+) channels.

Authors:  Nadia Jaafari; Elodie Marret; Marco Canepari
Journal:  Neurophotonics       Date:  2015-02-11       Impact factor: 3.593

2.  Imaging fast calcium currents beyond the limitations of electrode techniques.

Authors:  Nadia Jaafari; Michel De Waard; Marco Canepari
Journal:  Biophys J       Date:  2014-09-16       Impact factor: 4.033

3.  Calcium imaging at kHz frame rates resolves millisecond timing in neuronal circuits and varicosities.

Authors:  Michiel A Martens; Werend Boesmans; Pieter Vanden Berghe
Journal:  Biomed Opt Express       Date:  2014-07-16       Impact factor: 3.732

4.  A rapid and sensitive assay of intercellular coupling by voltage imaging of gap junction networks.

Authors:  Federico Ceriani; Fabio Mammano
Journal:  Cell Commun Signal       Date:  2013-10-21       Impact factor: 5.712

  4 in total

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