SynapTrack: An automated tool for synapse quantification

IF 1.9 4区 工程技术 Q3 MICROSCOPY
Journal of microscopy Pub Date : 2026-10-21 Epub Date: 2026-08-06 DOI:10.1111/jmi.70157
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.

SynapTrack:用于突触量化的自动化工具。
可靠的突触量化仍然具有挑战性,特别是在高通量荧光成像工作流程中。在这里,我们介绍了SynapTrack,这是一种全自动的基于FIJI/ imagej的工具,用于量化培养神经元和脑组织切片中的突触,只需最少的用户干预。SynapTrack结合了通道特定的预处理、背景减法和基于synquantum的共定位突触前和突触后点检测。在培养的神经元中,它还测量细胞数量和总树突长度,使每个细胞和每10微米树突的突触计数正常化。利用海马体培养,SynapTrack可靠地量化了兴奋性和抑制性突触,捕获了预期的兴奋性接触优势,并通过结构正常化减少了样本间的可变性。与SynBot相比,SynapTrack检测到更多的突触,同时更好地保留了突触类型之间有生物学意义的差异。对于细胞计数和树突分割不切实际的组织切片,我们开发了SynapTrack_Tissue,这是一种仅基于突触前-突触后共定位的适应性工作流。尽管缺乏细胞正常化,这种方法产生了跨异质神经区域的稳定测量。因为所有的空间参数都以微米为单位定义,所以分析设置在成像系统之间是便携式的。因此,SynapTrack为培养神经元和组织切片的突触量化提供了一个标准化和可扩展的框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of microscopy
Journal of microscopy 工程技术-显微镜技术
CiteScore
4.30
自引率
5.00%
发文量
83
审稿时长
1 months
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.
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