TY - JOUR
T1 - An R-CaMP1.07 reporter mouse for cell-type-specific expression of a sensitive red fluorescent calcium indicator
AU - Bethge, Philipp
AU - Carta, Stefano
AU - Lorenzo, Dayra A.
AU - Egolf, Ladan
AU - Goniotaki, Despoina
AU - Madisen, Linda
AU - Voigt, Fabian F.
AU - Chen, Jerry L.
AU - Schneider, Bernard
AU - Ohkura, Masamichi
AU - Nakai, Junichi
AU - Zeng, Hongkui
AU - Aguzzi, Adriano
AU - Helmchen, Fritjof
N1 - Funding Information:
This work was supported by grants from the Swiss National Science Foundation (31003A-149858; F.H.; and Sinergia grant CRSII3_147660; A.A., F.H., and B.S.; www.snf.ch ), the U.S. BRAIN Initiative (NIH grant 1U01NS090475-01; F.H.; www.braininitiative.nih.gov ), a Human Frontier 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 ). This work was also partially supported by the Regional Innovation Cluster Program (City Area Type, Central Saitama Area) (J.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.). H.Z. and L.M. thank the founders of the Allen Institute ( www.alleninstitute.org ), Paul G. Allen and Jody Allen, for their vision, encouragement, and support. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Publisher Copyright:
© 2017 Bethge et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2017/6
Y1 - 2017/6
N2 - 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.
AB - 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.
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U2 - 10.1371/journal.pone.0179460
DO - 10.1371/journal.pone.0179460
M3 - Article
C2 - 28640817
AN - SCOPUS:85021199764
SN - 1932-6203
VL - 12
JO - PLoS ONE
JF - PLoS ONE
IS - 6
M1 - e0179460
ER -