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A Tissue Clearing Method for Neuronal Imaging from Mesoscopic to Microscopic Scales
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DLA based compressed sensing for high resolution MR microscopy of neuronal tissue
Khieu-Van Nguyen1, Jing-Rebecca Li2, Guillaume Radecki3
1Neurospin, CEA Saclay, 91191 Gif sur Yvette, France; University Paris-Sud, XI, 91450 Orsay, France.
Journal of Magnetic Resonance (San Diego, Calif. : 1997)
|September 15, 2015
Summary
Compressed sensing (CS) using a novel diffusion limited aggregation (DLA) trajectory on a 17.2 T preclinical scanner accelerates imaging. This method enhances image quality for neuronal tissue analysis, outperforming traditional undersampling techniques.
Area of Science:
- Magnetic Resonance Imaging
- Biomedical Engineering
- Neuroscience
Background:
- Compressed sensing (CS) enables faster MRI by reconstructing images from undersampled data.
- Traditional CS undersampling methods often rely on polynomial probability density functions.
- High-field preclinical MRI scanners offer advanced imaging capabilities but require efficient acquisition strategies.
Purpose of the Study:
- To implement and evaluate a novel compressed sensing (CS) undersampling trajectory based on the diffusion limited aggregation (DLA) random growth model on a 17.2 T preclinical scanner.
- To compare the performance of the DLA-based CS undersampling with traditional polynomial probability density function-based undersampling.
- To assess the applicability of this DLA-CS method for imaging live neuronal tissues and its impact on acquisition time and image quality for automated cell segmentation.
Main Methods:
- Implementation of a diffusion limited aggregation (DLA) random growth model for generating undersampling trajectories.
- Application of the DLA-based CS method on a high-field (17.2 T) preclinical MRI scanner.
- Testing the method on a library of images and live neuronal tissues.
- Utilizing an automatic cell segmentation algorithm to evaluate image quality.
Main Results:
- The DLA-based CS undersampling trajectory demonstrated superior performance compared to traditional polynomial probability density function-based undersampling on a tested image library.
- The DLA-CS method was successfully applied to imaging live neuronal tissues.
- Significantly shorter acquisition times were achieved while preserving image quality sufficient for automatic neuron identification.
Conclusions:
- The diffusion limited aggregation (DLA) trajectory offers an effective strategy for compressed sensing (CS) in high-field preclinical MRI.
- This novel undersampling approach improves imaging efficiency for neuronal tissues, enabling faster scans without compromising essential image quality for cellular analysis.

