High-resolution analysis of bound Ca2+in neurons and synapses

Author:

Bonnin Elisa A123ORCID,Golmohammadi Arash4ORCID,Rehm Ronja1,Tetzlaff Christian4,Rizzoli Silvio O123ORCID

Affiliation:

1. Department of Neuro- and Sensory Physiology, University Medical Center Göttingen, Göttingen, Germany

2. Excellence Cluster Multiscale Bioimaging (MBExC), Göttingen, Germany

3. Center for Biostructural Imaging of Neurodegeneration (BIN), University Medical Center Göttingen, Göttingen, Germany

4. Group of Computational Synaptic Physiology, Department of Neuro- and Sensory Physiology, University Medical Center Göttingen, Göttingen, Germany

Abstract

Calcium (Ca2+) is a well-known second messenger in all cells, and is especially relevant for neuronal activity. Neuronal Ca2+is found in different forms, with a minority being freely soluble in the cell and more than 99% being bound to proteins. Free Ca2+has received much attention over the last few decades, but protein-bound Ca2+has been difficult to analyze. Here, we introduce correlative fluorescence and nanoscale secondary ion mass spectrometry imaging as a tool to describe bound Ca2+. As expected, bound Ca2+is ubiquitous. It does not correlate to free Ca2+dynamics at the whole-neuron level, but does correlate significantly to the intensity of markers for GABAergic pre-synapse and glutamatergic post-synapses. In contrast, a negative correlation to pre-synaptic activity was observed, with lower levels of bound Ca2+observed in the more active synapses. We conclude that bound Ca2+may regulate neuronal activity and should receive more attention in the future.

Funder

Deutsche Forschungsgemeinschaft

Publisher

Life Science Alliance, LLC

Subject

Health, Toxicology and Mutagenesis,Plant Science,Biochemistry, Genetics and Molecular Biology (miscellaneous),Ecology

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