UMMS Affiliation

Department of Biochemistry and Molecular Pharmacology

Date

12-8-2015

Document Type

Article

Disciplines

Biochemistry | Cell Biology | Genetics

Abstract

The application of current channelrhodopsin-based optogenetic tools is limited by the lack of strict ion selectivity and the inability to extend the spectra sensitivity into the near-infrared (NIR) tissue transmissible range. Here we present an NIR-stimulable optogenetic platform (termed "Opto-CRAC") that selectively and remotely controls Ca2+ oscillations and Ca2+-responsive gene expression to regulate the function of non-excitable cells, including T lymphocytes, macrophages and dendritic cells. When coupled to upconversion nanoparticles, the optogenetic operation window is shifted from the visible range to NIR wavelengths to enable wireless photoactivation of Ca2+-dependent signaling and optogenetic modulation of immunoinflammatory responses. In a mouse model of melanoma by using ovalbumin as surrogate tumor antigen, Opto-CRAC has been shown to act as a genetically-encoded "photoactivatable adjuvant" to improve antigen-specific immune responses to specifically destruct tumor cells. Our study represents a solid step forward towards the goal of achieving remote control of Ca2+-modulated activities with tailored function.

Rights and Permissions

Citation: Elife. 2015 Dec 8;4. pii: e10024. doi: 10.7554/eLife.10024. Link to article on publisher's site

DOI of Published Version

10.7554/eLife.10024

Comments

© 2015, He et al. This article is distributed under the terms of theCreative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.

Related Resources

Link to Article in PubMed

Keywords

Calcium signaling, Immune response, Nanoparticles, Near infrared, Optogenetics, STIM1, biochemistry, cell biology, human, mouse

Journal Title

eLife

PubMed ID

26646180

Creative Commons License

Creative Commons Attribution 4.0 License
This work is licensed under a Creative Commons Attribution 4.0 License.

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