Abstract

Genetically encoded calcium indicators (GECIs) enable imaging of in vivo brain cell activity with high sensitivity and specificity. In contrast to viral infection or in utero electroporation, indicator expression in transgenic reporter lines is induced noninvasively, reliably, and homogenously. Recently, Cre/tTA-dependent reporter mice were introduced, which provide high-level expression of green fluorescent GECIs in a cell-type-specific and inducible manner when crossed with Cre and tTA driver mice. Here, we generated and characterized the first red-shifted GECI reporter line of this type using R-CaMP1.07, a red fluorescent indicator that is efficiently two-photon excited above 1000 nm. By crossing the new R-CaMP1.07 reporter line to Cre lines driving layer-specific expression in neocortex we demonstrate its high fidelity for reporting action potential firing in vivo, long-term stability over months, and versatile use for functional imaging of excitatory neurons across all cortical layers, especially in the previously difficult to access layers 4 and 6.

Highlights

  • Fluorescent activity sensors are widely used for measuring single-cell and neuronal population activity using various imaging techniques [1, 2]

  • We conclude that virally-expressed R-CaMP1.07 acts as a sensitive and fast red genetically-encoded calcium indicators (GECIs) suitable for deep in vivo calcium imaging

  • We presented a novel mouse reporter line that expresses the red calcium indicator R-CaMP1.07 in excitatory neurons of distinct cortical layers when crossed with the corresponding Cre line and tTA line and that reliably and sensitively reports action potential (AP)-evoked calcium transients in the labeled neuronal populations

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Summary

Introduction

Fluorescent activity sensors are widely used for measuring single-cell and neuronal population activity using various imaging techniques [1, 2]. Over the past 20 years, a multitude of genetically-encoded calcium indicators (GECIs) have been developed and continually improved, including single fluorescent protein sensors emitting in the green or red spectral range [3,4,5,6,7,8,9,10,11] as well as ratiometric sensors. Science Program (HFSP; www.hfsp.org) postdoctoral fellowship (P.B.), and a CandDoc Forschungskredit of the University of Zurich (D.A. L.; www.uzh.ch). N.), Grants-in-Aid KAKENHI from the Ministry of Education, Culture, Sports, Science and Technology (MEXT; www.mext.go.jp) and the Japan Society for the Promotion of Science (JSPS; www.jsps.go.jp) (M.O., J.N.) and the program for Brain Mapping by Integrated Neurotechnologies for Disease Studies (Brain/MINDS) from MEXT and the Japan Agency for Medical Research and Development (AMED; www.amed.go.jp) (J.N.). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript

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