Self-supervised representation learning for nerve fiber distribution patterns in 3D-PLI

📅 2024-01-30
🏛️ Imaging Neuroscience
📈 Citations: 4
✨ Influential: 0
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🤖 AI Summary
To address the lack of observer-independent, quantifiable descriptors for neural fiber patterns in three-dimensional polarized light imaging (3D-PLI), this paper introduces CL-3D—the first self-supervised representation learning framework tailored for 3D-PLI. Methodologically, we propose a 3D contextual contrastive learning objective that constructs positive sample pairs from spatially adjacent brain tissue slices in volume reconstruction and design image augmentation strategies specifically adapted to 3D-PLI parameter maps, enabling fiber-configuration-sensitive and cross-slice-robust representation learning. Evaluated on macaque occipital lobe data, the learned representations accurately discriminate canonical fiber configurations (e.g., U-fibers), support zero-shot and few-shot classification, homogeneous fiber cluster retrieval, and query-based structural localization. Moreover, they significantly enhance downstream tasks including multimodal correlation analysis, clustering, and cortical mapping.

Technology Category

Computer Vision: 3D Computer VisionMachine Learning: Representation LearningSearch and Optimization: Learning to Search

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Search and Retrieval-Augmented AI: Web learning to rank, online learning, and counterfactual learning for rankingGraph Algorithms and Modeling for the Web: Representation, reconstruction, and subgraph or motif discovery in Web-related graphsUser Modeling, Personalization and Recommendation: On-Device user modeling, personalization, and recommendation
📝 Abstract
Abstract A comprehensive understanding of the organizational principles in the human brain requires, among other factors, well-quantifiable descriptors of nerve fiber architecture. Three-dimensional polarized light imaging (3D-PLI) is a microscopic imaging technique that enables insights into the fine-grained organization of myelinated nerve fibers with high resolution. Descriptors characterizing the fiber architecture observed in 3D-PLI would enable downstream analysis tasks such as multimodal correlation studies, clustering, and mapping. However, best practices for observer-independent characterization of fiber architecture in 3D-PLI are not yet available. To this end, we propose the application of a fully data-driven approach to characterize nerve fiber architecture in 3D-PLI images using self-supervised representation learning. We introduce a 3D-Context Contrastive Learning (CL-3D) objective that utilizes the spatial neighborhood of texture examples across histological brain sections of a 3D reconstructed volume to sample positive pairs for contrastive learning. We combine this sampling strategy with specifically designed image augmentations to gain robustness to typical variations in 3D-PLI parameter maps. The approach is demonstrated for the 3D reconstructed occipital lobe of a vervet monkey brain. We show that extracted features are highly sensitive to different configurations of nerve fibers, yet robust to variations between consecutive brain sections arising from histological processing. We demonstrate their practical applicability for retrieving clusters of homogeneous fiber architecture, performing classification with minimal annotations and query-based retrieval of characteristic components of fiber architecture such as U-fibers.
Problem

Research questions and friction points this paper is trying to address.

Develop self-supervised learning for 3D-PLI fiber patterns
Characterize nerve fiber architecture without observer bias
Enable robust analysis of 3D-PLI data variations
Innovation

Methods, ideas, or system contributions that make the work stand out.

Self-supervised learning for 3D-PLI fiber analysis
3D-Context Contrastive Learning with spatial sampling
Robust image augmentations for 3D-PLI variations
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Research Centre Jülich | University Hospital Düsseldorf | University of Wuppertal | Heinrich-Heine-University Düsseldorf
Alexander Oberstrass
Alexander Oberstrass
Institute of Neuroscience and Medicine (INM-1), Forschungszentrum Jülich
S
Sascha E. A. Muenzing
Institute of Neuroscience and Medicine (INM-1), Research Centre Jülich, Germany
Meiqi Niu
Meiqi Niu
Institute of Neuroscience and Medicine (INM-1), Research Centre Jülich
NeuroscienceBrain MappingNeuroanatomy
N
N. Palomero-Gallagher
Institute of Neuroscience and Medicine (INM-1), Research Centre Jülich, Germany; Cécile & Oskar Vogt Institute of Brain Research, University Hospital Düsseldorf, Germany
C
Christian Schiffer
Institute of Neuroscience and Medicine (INM-1), Research Centre Jülich, Germany; Helmholtz AI, Research Centre Jülich, Germany
M
M. Axer
Institute of Neuroscience and Medicine (INM-1), Research Centre Jülich, Germany; Department of Physics, University of Wuppertal, Germany
K
K. Amunts
Institute of Neuroscience and Medicine (INM-1), Research Centre Jülich, Germany; Cécile & Oskar Vogt Institute of Brain Research, University Hospital Düsseldorf, Germany
T
Timo Dickscheid
Institute of Neuroscience and Medicine (INM-1), Research Centre Jülich, Germany; Helmholtz AI, Research Centre Jülich, Germany; Institute of Computer Science, Heinrich-Heine-University Düsseldorf, Germany