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Editorial ARTICLE

Front. Mol. Neurosci., 22 December 2015 | https://doi.org/10.3389/fnmol.2015.00076

Editorial: Application of Genetically Encoded Indicators to Mammalian Central Nervous System

  • 1Laboratory for Developmental Neurobiology, Brain Science Institute, RIKEN, Wako-shi, Japan
  • 2Central Institute for Experimental Animals, Kawasaki-shi, Japan

Genetically encoded indicators are fluorescent proteins engineered to change their optical properties and report the dynamics of intracellular molecules or voltage. Encoded in a relatively compact size of DNA (typically 2–3 kilobase pairs), they are readily compatible with standard gene delivery techniques, including viral vectors and transgenesis. They can be thus expressed in specific types of cells with the use of cell type-specific promoters and/or Cre-loxP recombination system, which makes them beneficial for disentangling the complex mammalian neural circuitry. Another unique advantage of genetically encoded indicators is that they can be stably expressed for a long period, which allows chronic tracking of the same neuronal ensemble by longitudinal imaging, and offers unprecedented opportunities to investigate the neural basis of development, learning, and disease.

Since the prototypical genetically encoded Ca2+ indicators (GECIs) were reported for the first time (Miyawaki et al., 1997), genetically encoded indicators have drastically evolved in terms of signal to noise ratio, response kinetics, and spectral variety. In this Research Topic, Tian and colleagues provide a review on genetically encoded indicators of neuronal activity in general, including GECIs, with a special focus on the GCaMP family (GECIs composed of a circularly permutated GFP, the Ca2+-binding protein calmodulin, and the calmodulin-binding peptide M13), as well as genetically encoded indicators of voltage and synaptic activity (Broussard et al.). Griesbeck and colleagues present an overall review of GECIs, covering from the basics of Ca2+ imaging in neurons to the description of latest variants, and also discuss recent studies where GECIs were applied to neuronal population imaging in awake head-restrained mice (Rose et al.). The article by Nagai and colleagues focuses on affinity variants, color variants and photoactivatable variants of GECIs, the last two of which are of considerable importance for simultaneous use with optogenetic tools (Nagai et al.). Lin and colleagues then provide a review, for the first time to our knowledge, on a rapidly growing subfamily of optogenetic tools—a group of photoactivatable effector proteins that control the dynamics of intracellular molecules, rather than the membrane voltage (Zhou et al.).

It is also noteworthy that an important update of red GECI, R-CaMP2 was recently published (Inoue et al., 2015), reflecting the highly active nature of this field. R-CaMP2 was shown to have fast kinetics, high linearity, and remarkable sensitivity to detect single action potentials, making it even competitive with the state-of-art green GECIs; the proof of principle experiments show that it can be simultaneously used with GCaMP and/or channelrhodopsin, paving the way to multicolor longitudinal imaging and all-optical manipulation/recording of neural activity. Another group is also developing different variants of red GECIs independently (Dana et al., 2014), and it would be interesting to see side-to-side comparison in the future.

More specific technical advances are also reported in this Research Topic. Knöpfel and colleagues characterize a new series of genetically encoded voltage indicators, with a chimeric voltage sensing-domain (fragments from the Ci-VSP and the Kv3.1 potassium channel) sandwiched by a FRET donor and acceptor (“butterfly” design; Mishina et al.). Tsutsui and colleagues present their attempts to turn a GFP variant into a genetically encoded chromophore optimized for second harmonic generation microscopy, which can be used for voltage imaging (Jinno et al.). White and colleagues describe a set of in utero electroporation vectors carrying genetically encoded Ca2+ indicators (GCaMP), and investigate Ca2+ dyanamics of astrocytes in rat organotypic slice culture (Gee et al.).

The improved performance and rich repertoire of genetically encoded indicators have stimulated their widespread application to biologically relevant questions. Tvrdik and colleagues demonstrate 2-photon Ca2+ imaging in transgenic mice expressing GCaMP in microglia, and study Ca2+ dynamics induced by lipopolysaccharide and focal laser injury (Pozner et al.). Ohki and colleagues perform wide-field Ca2+ imaging in transgenic mice expressing GCaMP broadly across the cortex, and identify two visual association areas that respond to drifting gratings, where they further examine the cellular responses by 2-photon imaging (Murakami et al.). Fletcher and colleagues also perform wide-field Ca2+ imaging in transgenic mice expressing GCaMP in excitatory output neurons in the olfactory bulb, and examine the circuit element responsible for olfactory habituation (Ogg et al.).

We thank all the authors and reviewers for their valuable contributions to our Research Topic, and sincerely hope that it will provide readers with useful information and inspiration for further innovation in the field.

Author Contributions

YY and KM conceived the overall plan of Research Topic, recruited contributors, and wrote the manuscript.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

This work was supported by JST International Cooperative Research Project–Solution Oriented Research for Science and Technology (KM); JSPS Grants-in-Aid for Scientific Research S (20220007, 25221002, to KM), JSPS Grant-in-Aid for Young Scientists (B) (24700401, to YY), RIKEN BSI Grant (KM), and the Special Postdoctoral Researchers Program in RIKEN (YY).

References

Dana, H., Sun, Y., Hasseman, J.-P., Tsegaye, G., Holt, G.-T., Fosque, B.-F., et al. (2014). “Improved red protein indicators for in vivo calcium imaging,” in Program#/Poster#: 566.06/VV68, Society for Neuroscience (Washington, DC).

Inoue, M., Takeuchi, A., Horigane, S.-I., Ohkura, M., Gengyo-Ando, K., Fujii, H., et al. (2015). Rational design of a high-affinity, fast, red calcium indicator R-CaMP2. Nat. Meth. 12, 64–70. doi: 10.1038/nmeth.3185

PubMed Abstract | CrossRef Full Text | Google Scholar

Miyawaki, A., Llopis, J., Heim, R., McCaffery, J. M., Adams, J. A., Ikura, M., et al. (1997). Fluorescent indicators for Ca2+ based on green fluorescent proteins and calmodulin. Nature 388, 882–887. doi: 10.1038/42264

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: genetically encoded sensors, fluorescent protein sensors, genetically encoded calcium indicators (GECIs), in vivo imaging, genetically encoded voltage sensor

Citation: Yamada Y and Mikoshiba K (2015) Editorial: Application of Genetically Encoded Indicators to Mammalian Central Nervous System. Front. Mol. Neurosci. 8:76. doi: 10.3389/fnmol.2015.00076

Received: 29 October 2015; Accepted: 23 November 2015;
Published: 22 December 2015.

Edited by:

Robert J. Harvey, University College London, UK

Reviewed by:

Joe Lynch, University of Queensland, Australia

Copyright © 2015 Yamada and Mikoshiba. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Yoshiyuki Yamada, yy@brain.riken.jp;
Katsuhiko Mikoshiba, mikosiba@brain.riken.jp

Present Address: Yoshiyuki Yamada, Department of Basic Neurosciences, University of Geneva, Geneva, Switzerland