Red Light Optogenetics in Neuroscience

Abstract
Optogenetics, a field concentrating on controlling cellular functions by means of light-activated proteins, has shown tremendous potential in neuroscience. It possesses superior spatiotemporal resolution compared to the surgical, electrical, and pharmacological methods traditionally used in studying brain function. A multitude of optogenetic tools for neuroscience have been created that, for example, enable the control of action potential generation via light-activated ion channels. Other optogenetic proteins have been used in the brain, for example, to control long-term potentiation or to ablate specific subtypes of neurons. In in vivo applications, however, the majority of optogenetic tools are operated with blue, green, or yellow light, which all have limited penetration in biological tissues compared to red light and especially infrared light. This difference is significant, especially considering the size of the rodent brain, a major research model in neuroscience. Our review will focus on the utilization of red light-operated optogenetic tools in neuroscience. We first outline the advantages of red light for in vivo studies. Then we provide a brief overview of the red light-activated optogenetic proteins and systems with a focus on new developments in the field. Finally, we will highlight different tools and applications, which further facilitate the use of red light optogenetics in neuroscience.
Main Authors
Format
Articles Review article
Published
2022
Series
Subjects
Publication in research information system
Publisher
Frontiers Media SA
The permanent address of the publication
https://urn.fi/URN:NBN:fi:jyu-202201111074Use this for linking
Review status
Peer reviewed
ISSN
1662-5102
DOI
https://doi.org/10.3389/fncel.2021.778900
Language
English
Published in
Frontiers in Cellular Neuroscience
Citation
License
CC BY 4.0Open Access
Funder(s)
Research Council of Finland
Finnish Cultural Foundation
Research Council of Finland
Funding program(s)
Academy Research Fellow, AoF
Academy Project, AoF
Akatemiatutkija, SA
Akatemiahanke, SA
Research Council of Finland
Additional information about funding
This work was supported by the Academy of Finland grants 321522 (MN) and 330678 (HT), and a research grant by the Finnish Cultural Foundation (HT, MN, and KL).
Copyright© 2022 Lehtinen, Nokia and Takala.

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