Abstract
Background: Recent advances in genetically engineered calcium and membrane potential indicators provide the potential to estimate the activation dynamics of individual neurons within larger, mesoscale networks (100s-1000. +. neurons). However, a fully integrated automated workflow for the analysis and visualization of neural microcircuits from high speed fluorescence imaging data is lacking. New method: Here we introduce FluoroSNNAP, Fluorescence Single Neuron and Network Analysis Package. FluoroSNNAP is an open-source, interactive software developed in MATLAB for automated quantification of numerous biologically relevant features of both the calcium dynamics of single-cells and network activity patterns. FluoroSNNAP integrates and improves upon existing tools for spike detection, synchronization analysis, and inference of functional connectivity, making it most useful to experimentalists with little or no programming knowledge. Results: We apply FluoroSNNAP to characterize the activity patterns of neuronal microcircuits undergoing developmental maturation in vitro. Separately, we highlight the utility of single-cell analysis for phenotyping a mixed population of neurons expressing a human mutant variant of the microtubule associated protein tau and wild-type tau. Comparison with existing method(s): We show the performance of semi-automated cell segmentation using spatiotemporal independent component analysis and significant improvement in detecting calcium transients using a template-based algorithm in comparison to peak-based or wavelet-based detection methods. Our software further enables automated analysis of microcircuits, which is an improvement over existing methods. Conclusions: We expect the dissemination of this software will facilitate a comprehensive analysis of neuronal networks, promoting the rapid interrogation of circuits in health and disease.
| Original language | English |
|---|---|
| Pages (from-to) | 26-38 |
| Number of pages | 13 |
| Journal | Journal of Neuroscience Methods |
| Volume | 243 |
| DOIs | |
| State | Published - Mar 1 2015 |
Bibliographical note
Publisher Copyright:© 2015.
Funding
Funding was provided by Department of Defense W911NF-10-1-0526 , NIH PO1 NS 056202 , NSF IOS-1353724 , NJCBIR CBIR14IRG019 , and NJCBIR multi-investigator grant CBIR12MIG011 . We thank Jing Guo and Virginia M. Y. Lee (University of Pennsylvania) for providing PS19 ± neurons and 17025 antibody.
| Funders | Funder number |
|---|---|
| National Science Foundation | CBIR12MIG011, NJCBIR CBIR14IRG019, IOS-1353724 |
| National Institutes of Health | PO1 NS 056202 |
| U.S. Department of Defense | W911NF-10-1-0526 |
| National Institute of Neurological Disorders and Stroke | R56NS088176 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Calcium imaging
- Event detection
- FluoroSNNAP
- Functional connectivity
- Neuronal phenotype
- Synchrony
ASJC Scopus subject areas
- General Neuroscience
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