Cell type-specific relationships between spiking and [Ca2+]i in neurons of the Xenopus tadpole olfactory bulb

Authors

  • Bei-Jung Lin,

    1. Institute of Physiology, University of Göttingen, Göttingen Germany
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  • Tsai-Wen Chen,

    1. Institute of Physiology, University of Göttingen, Göttingen Germany
    2. Bernstein Center for Computational Neuroscience, Göttingen, Germany
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  • Detlev Schild

    1. Institute of Physiology, University of Göttingen, Göttingen Germany
    2. Bernstein Center for Computational Neuroscience, Göttingen, Germany
    3. DFG-Research Center for Molecular Physiology of the Brain (CMPB), Göttingen, Germany
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  • This paper has online supplemental material.

Corresponding author D. Schild: Department of Neurophysiology and Cellular Biophysics, Institute of Physiology, University of Göttingen, Humboldtallee 23, 37073 Göttingen, Germany. Email: dschild@gwdg.de

Abstract

Multi-neuronal recordings with Ca2+ indicator dyes usually relate [Ca2+]i to action potentials (APs) assuming a stereotypical dependency between the two. However, [Ca2+]i affects and is affected by numerous complex mechanisms that differ from cell type to cell type, from cell compartment to cell compartment. Moreover, [Ca2+]i depends on the specific way a cell is activated. Here we investigate, by combining calcium imaging and on-cell patch clamp recordings, the relationship between APs (spiking) and somatic [Ca2+]i in mitral and granule cells of the olfactory bulb in Xenopus laevis tadpoles. Both cell types exhibit ongoing and odour-modulated [Ca2+]i dynamics. In mitral cells, the occurrence of APs in both spontaneous and odour-evoked situations correlates tightly to step-like [Ca2+]i increases. Moreover, odorant-induced suppression of spontaneous firing couples to a decrease in [Ca2+]i. In contrast, granule cells show a substantial number of uncorrelated events such as increases in [Ca2+]i without APs occurring or APs without any effect upon [Ca2+]i. The correlation between spiking and [Ca2+]i is low, possibly due to somatic NMDAR-mediated and subthreshold voltage-activated Ca2+ entries, and thus does not allow a reliable prediction of APs based on calcium imaging. Taken together, our results demonstrate that the relationship between somatic [Ca2+]i and APs can be cell type specific. Taking [Ca2+]i dynamics as an indicator for spiking activity is thus only reliable if the correlation has been established in the system of interest. When [Ca2+]i and APs are precisely correlated, fast calcium imaging is an extremely valuable tool for determining spatiotemporal patterns of APs in neuronal population.

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