Non-invasive optical control of endogenous Ca<sup>2+</sup> channels in awake mice.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 31924789.
- Also identified by DOI 10.1038/s41467-019-14005-4 and PMC identifier 6954201.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Optogenetic approaches for controlling Ca<sup>2+</sup> channels provide powerful means for modulating diverse Ca<sup>2+</sup>-specific biological events in space and time. However, blue light-responsive photoreceptors are, in principle, considered inadequate for deep tissue stimulation unless accompanied by optic fiber insertion. Here, we present an ultra-light-sensitive optogenetic Ca<sup>2+</sup> modulator, named monSTIM1 encompassing engineered cryptochrome2 for manipulating Ca<sup>2+</sup> signaling in the brain of awake mice through non-invasive light delivery. Activation of monSTIM1 in either excitatory neurons or astrocytes of mice brain is able to induce Ca<sup>2+</sup>-dependent gene expression without any mechanical damage in the brain. Furthermore, we demonstrate that non-invasive Ca<sup>2+</sup> modulation in neurons can be sufficiently and effectively translated into changes in behavioral phenotypes of awake mice.
Medical subject headings
- Calcium Channels
- Cryptochromes
- Fiber Optic Technology
- Optogenetics
- Stromal Interaction Molecule 1