Groschup, Bernhard; Calandra, Gian Marco; Raitmayr, Constanze; Shrouder, Joshua; Llovera, Gemma; Zaki, Asal Ghaffari; Burgstaller, Sandra; Bischof, Helmut; Eroglu, Emrah; Liesz, Arthur; Malli, Roland; Filser, Severin; Plesnila, Nikolaus (2024): Probing intracellular potassium dynamics in neurons with the genetically encoded sensor lc-LysM GEPII 1.0 in vitro and in vivo. Scientific Reports, 14 (1). ISSN 2045-2322
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Abstract
Neuronal activity is accompanied by a net outflow of potassium ions (K+) from the intra- to the extracellular space. While extracellular [K+] changes during neuronal activity are well characterized, intracellular dynamics have been less well investigated due to lack of respective probes. In the current study we characterized the FRET-based K+ biosensor lc-LysM GEPII 1.0 for its capacity to measure intracellular [K+] changes in primary cultured neurons and in mouse cortical neurons in vivo. We found that lc-LysM GEPII 1.0 can resolve neuronal [K+] decreases in vitro during seizure-like and intense optogenetically evoked activity. [K+] changes during single action potentials could not be recorded. We confirmed these findings in vivo by expressing lc-LysM GEPII 1.0 in mouse cortical neurons and performing 2-photon fluorescence lifetime imaging. We observed an increase in the fluorescence lifetime of lc-LysM GEPII 1.0 during periinfarct depolarizations, which indicates a decrease in intracellular neuronal [K+]. Our findings suggest that lc-LysM GEPII 1.0 can be used to measure large changes in [K+] in neurons in vitro and in vivo but requires optimization to resolve smaller changes as observed during single action potentials.
Doc-Type: | Article (LMU Hospital) |
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Organisational unit (Faculties): | 07 Medicine > Medical Center of the University of Munich > Institute for Stroke and Dementia Research (ISD) |
DFG subject classification of scientific disciplines: | Life sciences |
Date Deposited: | 27. Sep 2024 13:04 |
Last Modified: | 27. Sep 2024 13:04 |
URI: | https://oa-fund.ub.uni-muenchen.de/id/eprint/1497 |
DFG: | Funded by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) - 491502892 |