Label-free 3D-CLEM Using Endogenous Tissue Landmarks
Manja Luckner,
Steffen Burgold,
Severin Filser,
Maximilian Scheungrab,
Yilmaz Niyaz,
Eric Hummel,
Gerhard Wanner,
Jochen Herms
Affiliations
Manja Luckner
Department of Biology I, Biocenter Ludwig-Maximilians-University Munich, Planegg-Martinsried 82152, Germany; German Center for Neurodegenerative Diseases (DZNE), Translational Brain Research, Munich 81377, Germany
Steffen Burgold
German Center for Neurodegenerative Diseases (DZNE), Translational Brain Research, Munich 81377, Germany; Center for Neuropathology, Ludwig-Maximilians-University Munich, Munich 81377, Germany; Carl Zeiss Microscopy, Oberkochen 73447, Germany
Severin Filser
German Center for Neurodegenerative Diseases (DZNE), Translational Brain Research, Munich 81377, Germany
Maximilian Scheungrab
Department of Biology I, Biocenter Ludwig-Maximilians-University Munich, Planegg-Martinsried 82152, Germany
Yilmaz Niyaz
Carl Zeiss Microscopy, Oberkochen 73447, Germany
Eric Hummel
Carl Zeiss Microscopy, Oberkochen 73447, Germany
Gerhard Wanner
Department of Biology I, Biocenter Ludwig-Maximilians-University Munich, Planegg-Martinsried 82152, Germany
Jochen Herms
Department of Biology I, Biocenter Ludwig-Maximilians-University Munich, Planegg-Martinsried 82152, Germany; German Center for Neurodegenerative Diseases (DZNE), Translational Brain Research, Munich 81377, Germany; Center for Neuropathology, Ludwig-Maximilians-University Munich, Munich 81377, Germany; Munich Cluster of Systems Neurology (SyNergy), Munich 81377, Germany; Corresponding author
Summary: Emerging 3D correlative light and electron microscopy approaches enable studying neuronal structure-function relations at unprecedented depth and precision. However, established protocols for the correlation of light and electron micrographs rely on the introduction of artificial fiducial markers, such as polymer beads or near-infrared brandings, which might obscure or even damage the structure under investigation. Here, we report a general applicable “flat embedding” preparation, enabling high-precision overlay of light and scanning electron micrographs, using exclusively endogenous landmarks in the brain: blood vessels, nuclei, and myelinated axons. Furthermore, we demonstrate feasibility of the workflow by combining in vivo 2-photon microscopy and focused ion beam scanning electron microscopy to dissect the role of astrocytic coverage in the persistence of dendritic spines. : Neuroscience; Techniques in Neuroscience; Biological Sciences Research Methodologies; Biological Sciences Tools Subject Areas: Neuroscience, Techniques in Neuroscience, Biological Sciences Research Methodologies, Biological Sciences Tools