Carlos Gallego-García, Elena Martínez-Blanco, F. Javier Díez-Guerra
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引用次数: 0
Abstract
Reliable synapse quantification remains challenging, particularly in high-throughput fluorescence imaging workflows. Here we present SynapTrack, a fully automated FIJI/ImageJ-based tool for quantifying synapses in cultured neurons and brain tissue sections with minimal user intervention. SynapTrack combines channel-specific preprocessing, background subtraction, and SynQuant-based detection of colocalised pre- and postsynaptic puncta. In cultured neurons, it additionally measures cell number and total dendritic length, enabling normalisation of synapse counts per cell and per 10 micrometer of dendrite. Using hippocampal cultures, SynapTrack reliably quantified excitatory and inhibitory synapses, captured the expected predominance of excitatory contacts, and reduced inter-sample variability through structural normalisation. Compared with SynBot, SynapTrack detected more synapses while better preserving biologically meaningful differences between synapse types. For tissue sections, in which cell counting and dendritic segmentation are impractical, we developed SynapTrack_Tissue, an adapted workflow based on presynaptic-postsynaptic colocalisation alone. Despite the lack of cellular normalisation, this approach produced stable measurements across heterogeneous neuropil regions. Because all spatial parameters are defined in micrometres, analysis settings are portable across imaging systems. SynapTrack therefore provides a standardised and scalable framework for synapse quantification in both cultured neurons and tissue sections.
期刊介绍:
The Journal of Microscopy is the oldest journal dedicated to the science of microscopy and the only peer-reviewed publication of the Royal Microscopical Society. It publishes papers that report on the very latest developments in microscopy such as advances in microscopy techniques or novel areas of application. The Journal does not seek to publish routine applications of microscopy or specimen preparation even though the submission may otherwise have a high scientific merit.
The scope covers research in the physical and biological sciences and covers imaging methods using light, electrons, X-rays and other radiations as well as atomic force and near field techniques. Interdisciplinary research is welcome. Papers pertaining to microscopy are also welcomed on optical theory, spectroscopy, novel specimen preparation and manipulation methods and image recording, processing and analysis including dynamic analysis of living specimens.
Publication types include full papers, hot topic fast tracked communications and review articles. Authors considering submitting a review article should contact the editorial office first.