Bicistronic expression of a high-performance calcium indicator and opsin yields stable, robust cortical expression for holographic two-photon stimulation
Paul K. LaFosseiD, Zhishang ZhouiD, Nina G. FriedmaniD, Yanting DengiD, Anna J. LiiD, Bradley AkitakeiD, Mark H. HistediD
Abstract
Patterns of activity across many neurons are fundamental units of neural computation. Two-photon holographic photostimulation allows both delivering input to, and imaging responses from, patterns or populations of neurons. However, to make this method an easily-deployable tool, simple methods are needed to robustly and stably express opsins and indicators in the same cells. Here we describe a bicistronic adeno-associated virus (AAV) that in transfected cells expresses both the fast and bright calcium indicator GCaMP8s, and a soma-targeted (st) and two-photon-activatable opsin, ChrimsonR. With this method, in the visual cortex of mice, stChrimsonR stimulation with two-photon holography drives robust spiking in targeted cells, and neural responses to visual sensory stimuli and spontaneous activity are strong and easy to measure. stChrimsonR is a good choice of opsin when a balance is needed between stimulation-laser activatability and avoidance of imaging laser activation. This approach is a simple and robust way to prepare neurons in vivo for two-photon holography and imaging. Significance statementThe recent advent of holographic photostimulation methods in conjunction with standard two-photon calcium imaging promises unprecedented levels of control in manipulating and dissecting brain circuitry in vivo while reading out neural activity. These all-optical methods rely on a working synergy between optogenetic strategies to both measure calcium activity through genetically-encoded calcium indicators and modulate cell activity through light-activated opsins. Genetic strategies to achieve reliable and stable co-expression of opsin and indicator remain sparse and often challenging to execute. Here, we present a genetic tool to achieve robust co-expression of jGCaMP8s indicator and stChrimsonR opsin via a single injected virus to help facilitate experiments aiming to use holography to investigate the circuit principles underlying brain activity.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 17
- FWCI
- 2.06
- Field percentile
- top 13%
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Parallel holographic illumination enables sub-millisecond two-photon optogenetic activation in mouse visual cortex in vivo
I-Wen Chen, Emiliano Ronzitti, … Valentina Emiliani·bioRxiv·Jan 21, 2018
- Three-Dimensional Two-Photon Optogenetics And Imaging Of Neural Circuits In Vivo
Weijian Yang, Luis Carrillo‐Reid, … Rafael Yuste·eLifePeer-reviewed·Feb 7, 2018
- Computational optimization of two-photon holographic stimulation sites in vivo
Marcus A. Triplett, Edgar Bäumler, … Liam Paninski·bioRxiv·Jul 31, 2025
- Multiphoton holographic photostimulation induces potassium-dependent spike silencing in label-free mouse cortex in vivo
Stylianos Papaioannou, Johan Zakrisson, … Paolo Medini·bioRxiv·Aug 6, 2022
- Sub-millisecond optogenetic control of neuronal firing with two-photon holographic photoactivation of Chronos
Emiliano Ronzitti, Rossella Conti, … Valentina Emiliani·bioRxiv·Jul 5, 2016
- Navigating the translational roadblock: Towards highly specific and effective all-optical interrogations of neural circuits
Ting Fu, Isabelle Arnoux, … Albrecht Stroh·bioRxiv·Apr 20, 2020