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Single-spike detection in vitro and in vivo with a genetic Ca2+ sensor

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Wallace,  DJ
Max Planck Institute for Biological Cybernetics, Max Planck Society;
Former Research Group Network Imaging, Max Planck Institute for Biological Cybernetics, Max Planck Society;
Research Group Neural Population Imaging, Max Planck Institute for Biological Cybernetics, Max Planck Society;

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Kerr,  JND
Max Planck Institute for Biological Cybernetics, Max Planck Society;
Former Research Group Network Imaging, Max Planck Institute for Biological Cybernetics, Max Planck Society;
Research Group Neural Population Imaging, Max Planck Institute for Biological Cybernetics, Max Planck Society;

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Citation

Wallace, D., Meyer zum Alten Borgloh, S., Astori, S., Yang, Y., Bausen, M., Kügler, S., et al. (2008). Single-spike detection in vitro and in vivo with a genetic Ca2+ sensor. Nature methods, 5(9), 797-804. doi:10.1038/nmeth.1242.


Cite as: http://hdl.handle.net/11858/00-001M-0000-0013-C797-A
Abstract
Measurement of population activity with single-action-potential, single-neuron resolution is pivotal for understanding information representation and processing in the brain and how the brain‘s responses are altered by experience. Genetically encoded indicators of neuronal activity allow long-term, cell type–specific expression. Fluorescent Ca2+ indicator proteins (FCIPs), a main class of reporters of neural activity, initially suffered, in particular, from an inability to report single action potentials in vivo. Although suboptimal Ca2+-binding dynamics and Ca2+-induced fluorescence changes in FCIPs are important factors, low levels of expression also seem to play a role. Here we report that delivering D3cpv, an improved fluorescent resonance energy transfer–based FCIP, using a recombinant adeno-associated virus results in expression sufficient to detect the Ca2+ transients that accompany single action potentials. In upper-layer cortical neurons, we were able to detect transients associated with single action potentials firing at rates of