New imaging technique provides structural information about brain tissue

    22 March 2019


    Diattenuation Imaging (DI) analyses thin histological brain sections in a special microscope that uses polarized light, i.e. a light wave with a certain direction of oscillation. 

    A new method called Diattenuation Imaging, which was developed by HBP scientists at Forschungszentrum Jülich in collaboration with the University of Groningen, reveals image contrasts between different tissue types of the brain and allows distinguishing regions with many thin nerve fibres from regions with few thick nerve fibres. The technique can be used in addition to other imaging modalities to learn more about the brain’s nerve fibre architecture and tissue composition, and to identify pathological changes.

    Diattenuation Imaging (DI) provides image contrasts between different brain tissue types. Copyright: Miriam Menzel et al., Scientific Reports (2019), DOI:10.1038/s41598-019-38506-w (CC BY 4.0)

    Diattenuation Imaging (DI) analyses thin histological brain sections in a special microscope that uses polarized light, i.e. a light wave with a certain direction of oscillation. The technique is an extension of the previously established method of 3D Polarized Light Imaging (3D-PLI), which  measures the polarization-dependent refraction of light to derive the spatial orientations of the nerve fibres. 

    The new technique combines the 3D-PLI measurement with a diattenuation measurement, which determines the polarization-dependent attenuation of light (diattenuation). The scientists found that in some regions, the brain tissue is maximally transparent when the polarization of light is oriented parallel to the nerve fibres. In other regions, the tissue is maximally transparent when the polarization is oriented perpendicularly to the nerve fibres.

    To study these effects in more detail, the researchers went on to model the propagation of the light wave through artificial nerve fibre configurations using simulations on the former Jülich supercomputer JUQUEEN. The simulations revealed that the observed effects do not only depend on the nerve fibre orientations and the time after embedding the brain sections, but also on other tissue properties like the fibre diameter or the thickness of the myelin sheaths, which surround many nerve fibres in the brain.

    This makes Diattenuation Imaging (DI) a valuable extension to 3D-PLI, enabling a more precise investigation of brain tissue. In the future, the DI method could be used, e.g., to investigate neurodegenerative diseases like multiple sclerosis or multisystem atrophy (MSA), which go along with alterations of the myelin sheath. In addition, the technology could help to make pathological changes visible and to identify connected regions and tissue types, providing more data for complex computational reconstructions of the brain. (text adapted with permission from Forschungszentrum Jülich)
     

    How it works

    3D-PLI (left) reveals the direction of the nerve fibres. A diattenuation measurement (right) reveals the direction of polarization for which a maximum amount of light passes through the brain section. Regions for which this polarization direction runs parallel (or perpendicular) to the fibre direction are marked in green (or magenta). Copyright: Forschungszentrum Jülich / Miriam Menzel, Tobias Schlößer

    The regional differences that become apparent with Diattenuation Imaging depend, among other things, on the time after embedding the brain sections (left: freshly measured brain section, right: 7 weeks later). Copyright: Miriam Menzel et al., Scientific Reports (2019), DOI:10.1038/s41598-019-38506-w (CC BY 4.0)

     

    Part of the HBP’s Human Brain Atlas
    The high quality data from this and other areas of HBP’s experimental neuroscience work is being integrated into a multiscale, multimodal 3D model to construct the most comprehensive atlas of the human brain to date. Neuroscientists and supercomputing experts work together to handle the extremely large datasets generated by modern neuroscience methods, and are developing the pioneering technology and workflows for investigating the brain with High Performance Computing. The resulting atlas and analytics tools are available to researchers around the world through their web browser.
    More information and access: https://www.humanbrainproject.eu/en/explore-the-brain/ 

    See also:


    Watch: Data integration and interactive use of HBP’s brain Atlas systems
    The HBP atlas systems offer a way to integrate vast and heterogeneous neuroscience data into common frameworks and better understand the multilevel organization of the brain. A new video explains the key principles of HBP workflows used for registration of data into common reference atlases.
    https://www.humanbrainproject.eu/en/follow-hbp/news/watch-data-integration-and-interactive-use-of-hbp-s-brain-atlas-systems/ 
     

    Understanding autism: novel brain imaging study challenges the dominant explanation
    Data obtained within HBP’s brain atlas work has contributed to the discovery of a "short distance" brain connectivity deficit that is associated with a lack of social interaction and empathy.
    https://www.humanbrainproject.eu/en/follow-hbp/news/understanding-autism-novel-brain-imaging-study-challenges-the-dominant-explanation/ 
     
    The hippocampus as never seen before
    HBP researchers have published a novel post-mortem mapping of the hippocampus at unprecedented resolution. This not only reveals the hippocampus' substructures, but also its internal connectivity and cellular composition.https://www.humanbrainproject.eu/en/follow-hbp/news/the-hippocampus-as-never-seen-before/ 

     

    Contact:
    Dr. Miriam Menzel
    Institute of Neuroscience and Medicine (INM-1), Forschungszentrum Jülich
    m.menzel@fz-juelich.de

    Original publication:
    Menzel M, Axer M, Amunts K, De Raedt H, Michielsen K.
    Diattenuation Imaging reveals different brain tissue properties.
    Sci Rep. 2019;9:1939 (published 2019 Feb 13), DOI: 10.1038/s41598-019-38506-w