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Nat Commun ; 15(1): 4102, 2024 May 22.
Article in English | MEDLINE | ID: mdl-38778027

ABSTRACT

The development of robust tools for segmenting cellular and sub-cellular neuronal structures lags behind the massive production of high-resolution 3D images of neurons in brain tissue. The challenges are principally related to high neuronal density and low signal-to-noise characteristics in thick samples, as well as the heterogeneity of data acquired with different imaging methods. To address this issue, we design a framework which includes sample preparation for high resolution imaging and image analysis. Specifically, we set up a method for labeling thick samples and develop SENPAI, a scalable algorithm for segmenting neurons at cellular and sub-cellular scales in conventional and super-resolution STimulated Emission Depletion (STED) microscopy images of brain tissues. Further, we propose a validation paradigm for testing segmentation performance when a manual ground-truth may not exhaustively describe neuronal arborization. We show that SENPAI provides accurate multi-scale segmentation, from entire neurons down to spines, outperforming state-of-the-art tools. The framework will empower image processing of complex neuronal circuitries.


Subject(s)
Algorithms , Brain , Imaging, Three-Dimensional , Neurons , Neurons/cytology , Animals , Brain/diagnostic imaging , Brain/cytology , Imaging, Three-Dimensional/methods , Mice , Image Processing, Computer-Assisted/methods
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