Towards automatic reconstruction of axonal structures in volumetric microscopy images depicting only active synapses

S. Sokoll, Hagen Beelitz, M. Heine, Klaus D. Tönnies
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Abstract

We propose an algorithm for the three-dimensional (3D) reconstruction of axonal structures to allow for the correlation of axonal structure, individual synaptic activity and single molecule tracking. In contrast to related works, only active synapses are stained in our acquisitions and the axonal structure is only visible by autofluorescence. We tackle this problem by detection of the medial axis line in the two-dimensional (2D) intensity projection of the 3D image and reconstruction of the 3D structure by axial interpolation between connected active synapses. Due to the noncontinuous staining, the detection of the medial axis line cannot rely on a global tree like structure. Instead, we compute an initial skeleton by global segmentation and expand it by iteratively adding line segments that are locally optimal according to the model knowledge of an axon. We evaluate our algorithm against a ground truth computed from co-transfection of surface molecules that result in reliable continuous staining of the axonal structure.
在仅描绘活跃突触的体积显微镜图像中实现轴突结构的自动重建
我们提出了一种三维(3D)重建轴突结构的算法,以允许轴突结构,单个突触活动和单分子跟踪的相关性。与相关研究相反,在我们的采集中,只有活跃的突触被染色,轴突结构只能通过自身荧光可见。我们通过检测三维图像的二维(2D)强度投影中的中轴线,并通过连接的活动突触之间的轴向插值重建三维结构来解决这个问题。由于不连续的染色,不能依靠全局树状结构来检测中轴线。相反,我们通过全局分割计算初始骨架,并通过根据轴突的模型知识迭代添加局部最优线段来扩展它。我们根据表面分子共转染计算的基础真理来评估我们的算法,结果是轴突结构的可靠连续染色。
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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