4.3 Article

Optogenetic activation of muscle contractionin vivo

Journal

CONNECTIVE TISSUE RESEARCH
Volume 62, Issue 1, Pages 15-23

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1080/03008207.2020.1798943

Keywords

Optogenetics; triceps surae; cre-lox; skeletal muscle; channelrhodopsin-2

Funding

  1. Eunice Kennedy Shriver National Institute of Child Health and Human Development [R03 HD094594]
  2. National Institute of Neurological Disorders and Stroke [R01 NS069777]

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This study aimed to evaluate the feasibility of non-invasive optogenetic stimulation of skeletal muscle in mice. By inducing specific gene expression in skeletal muscle and using transdermal blue light exposure for muscle contraction experiments, the study demonstrated the impact of optogenetic stimulation on sustained muscle contraction.
Purpose: Optogenetics is an emerging alternative to traditional electrical stimulation to initiate action potentials in activatable cells both ex vivo and in vivo. Optogenetics has been commonly used in mammalian neurons and more recently, it has been adapted for activation of cardiomyocytes and skeletal muscle. Therefore, the aim of this study was to evaluate the stimulation feasibility and sustain isometric muscle contraction and limit decay for an extended period of time (1s), using non-invasive transdermal light activation of skeletal muscle (triceps surae) in vivo. Materials and Methods We used inducible Cre recombination to target expression of Channelrhodopsin-2 (ChR2(H134R)-EYFP) in skeletal muscle (Acta1-Cre) in mice. Fluorescent imaging confirmed that ChR2 expression is localized in skeletal muscle and does not have specific expression in sciatic nerve branch, therefore, allowing for non-nerve mediated optical stimulation of skeletal muscle. We induced muscle contraction using transdermal exposure to blue light and selected 10 Hz stimulation after controlled optimization experiments to sustain prolonged muscle contraction. Results Increasing the stimulation frequency from 10 Hz to 40 Hz increased the muscle contraction decay during prolonged 1s stimulation, highlighting frequency dependency and importance of membrane repolarization for effective light activation. Finally, we showed that optimized pulsed optogenetic stimulation of 10 Hz resulted in comparable ankle torque and contractile functionality to that of electrical stimulation. Conclusions Our results demonstrate the feasibility and repeatability of non-invasive optogenetic stimulation of muscle in vivo and highlight optogenetic stimulation as a powerful tool for non-invasive in vivo direct activation of skeletal muscle.

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