This article is a correction to:
Imaging Calcium in Hippocampal Presynaptic Terminals With a Ratiometric Calcium Sensor in a Novel Transgenic Mouse
Ibrahim Al-Osta
Mariusz Mucha†
Daniel Pereda
Marta Piqué-Gili
Albert E. Okorocha†
Roisin Thomas
Nicholas A. Hartell*- Department of Neuroscience, Psychology and Behaviour, University of Leicester, Leicester, United Kingdom
A Corrigendum on
Imaging Calcium in Hippocampal Presynaptic Terminals With a Ratiometric Calcium Sensor in a Novel Transgenic Mouse
by Al-Osta, I., Mucha, M., Pereda, D., Piqué-Gili, M., Okorocha, A. E., Thomas, R., et al. (2018). Front. Cell. Neurosci. 12:209. doi: 10.3389/fncel.2018.00209
In the original article, there was a mistake in Figure 8 as published. During the revision process, panels B-G from Figure 2 were incorrectly duplicated into panels B-G of Figure 8. The data for these figures were correct in the original submission. The corrected Figure 8 appears below. The authors apologize for this error and state that this does not change the scientific conclusions of the article in any way. The original article has been updated.
FIGURE 8
Figure 8. Effect of stimulus intensity on fluorescence responses recorded from the CA3 region of the hippocampus in SyGCaMP2-mCherry expressing mice. Bursts of 10 stimuli over a range of intensities were delivered at 20 Hz via a patch pipette placed s. granulosum of the dentate gyrus. Images of SyGCaMP2 (green) and mCherry fluorescence (red) are shown along with the ratio of the two and images illustrating the difference in fluorescence for each fluorophore and their ratio before and during stimulation at each intensity labeled (A). The positions of the stimulating and recording electrodes are marked with upper and lower asterisks respectively. Abbreviations: pcl; pyramidal cell layer; sg; s. granulosum; sl; stratum lucidum. The horizontal scale bar represents 100 μm. Responses over time are shown (B) for SyGCaMP2 and mCherry fluorescence extracted from ROIs placed over the s lucidum (sl). The ratios of SyGCaMP2:mCherry fluorescence at each intensity are shown in blue. Increasing intensities are depicted with darker hues. The mean and SEM peak (C), initial slope (D) and decay time constant (E) of SyGCaMP2 fluorescence responses and the N2 component of fEPSPs (F) are plotted against intensity. The relationship between SyGCaMP2 and N2 peak responses is shown in panel (G). A line of best fit was plotted for values measured below 50 V where the relationship was linear. Data were obtained from six separate hippocampal slices taken from four different mice.
Keywords: presynaptic terminals, calcium imaging, transgenic mice, hippocampus, CA1, CA3, long-term potentiation
Citation: Al-Osta I, Mucha M, Pereda D, Piqué-Gili M, Okorocha AE, Thomas R and Hartell NA (2019) Corrigendum: Imaging Calcium in Hippocampal Presynaptic Terminals With a Ratiometric Calcium Sensor in a Novel Transgenic Mouse. Front. Cell. Neurosci. 13:194. doi: 10.3389/fncel.2019.00194
Received: 15 April 2019; Accepted: 18 April 2019;
Published: 15 May 2019.
Approved by:
Frontiers in Cellular Neuroscience Editorial Office, Frontiers Media SA, SwitzerlandCopyright © 2019 Al-Osta, Mucha, Pereda, Piqué-Gili, Okorocha, Thomas and Hartell. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Nicholas A. Hartell, bmg4OEBsZS5hYy51aw==; bmljaG9sYXMuaGFydGVsbEBnbWFpbC5jb20=
†Present Address: Mariusz Mucha, Laboratory of Neuronal Plasticity and Behaviour, University of Exeter Medical School, University of Exeter, Exeter, United Kingdom
Albert E. Okorocha, Department of Physiology, Faculty of Basic Medical Sciences, Ebonyi State University, Ebonyi, Nigeria