Optimized temporally deconvolved Ca2+ imaging allows identification of spatiotemporal activity patterns of CA1 hippocampal ensembles

• Verfasst von: Pfeiffer, Thomas [VerfasserIn]
• Verfasst von: Draguhn, Andreas [VerfasserIn]
• Verfasst von: Reichinnek, Susanne [VerfasserIn]
• Verfasst von: Both, Martin [VerfasserIn]
• Titel: Optimized temporally deconvolved Ca2+ imaging allows identification of spatiotemporal activity patterns of CA1 hippocampal ensembles
• Verf.angabe: Thomas Pfeiffer, Andreas Draguhn, Susanne Reichinnek, Martin Both
• E-Jahr: 2014
• Jahr: 17 March 2014
• Umfang: 11 S.
• Fussnoten: Im Titel ist "2+" in Ca2+ hochgestellt ; Gesehen am 23.07.2020
• Titel Quelle: Enthalten in: NeuroImage
• Ort Quelle: Orlando, Fla. : Academic Press, 1992
• Jahr Quelle: 2014
• Band/Heft Quelle: 94(2014), Seite 239-249
• ISSN Quelle: 1095-9572
• DOI: doi:10.1016/j.neuroimage.2014.03.030
• Datenträger: Online-Ressource
• Sprache: eng
• Sach-SW: Ca imaging
• Sach-SW: Hippocampal ensembles
• Sach-SW: Neuronal network topology
• Sach-SW: Optimized reconstruction of neuronal firing behavior
• K10plus-PPN: 1725358956

Abstract

Hippocampal activity is characterized by the coordinated firing of a subset of neurons. Such neuronal ensembles can either be driven by external stimuli to form new memory traces or be reactivated by intrinsic mechanisms to reactivate and consolidate old memories. Hippocampal network oscillations orchestrate this coherent activity. One key question is how the topology, i.e. the functional connectivity of neuronal networks supports their desired function. Recently, this has been addressed by characterizing the intrinsic properties for the highly recurrently connected CA3 region using organotypic slice cultures and Ca2+ imaging. In the present study, we aimed to determine the properties of CA1 hippocampal ensembles at high temporal and multiple single cell resolution. Thus, we performed Ca2+ imaging using the chemical fluorescent Ca2+ indicator Oregon Green BAPTA 1-AM. To achieve most physiological conditions, we used acute hippocampal slices that were recorded in a so-called interface chamber. To faithfully reconstruct firing patterns of multiple neurons in the field of view, we optimized deconvolution-based detection of action potential associated Ca2+ events. Our approach outperformed currently available detection algorithms by its sensitivity and robustness. In combination with advanced network analysis, we found that acute hippocampal slices contain a median of 11 CA1 neuronal ensembles with a median size of 4 neurons. This apparently low number of neurons is likely due to the confocal imaging acquisition and therefore yields a lower limit. The distribution of ensemble sizes was compatible with a scale-free topology, as far as can be judged from data with small cell numbers. Interestingly, cells were more tightly clustered in large ensembles than in smaller groups. Together, our data show that spatiotemporal activity patterns of hippocampal neuronal ensembles can be reliably detected with deconvolution-based imaging techniques in mouse hippocampal slices. The here presented techniques are fully applicable to similar studies of distributed optical measurements of neuronal activity (in vivo), where signal-to-noise ratio is critical.