Multiscale ATUM-FIB Microscopy Enables Targeted Ultrastructural Analysis at Isotropic Resolution
Georg Kislinger,
Helmut Gnägi,
Martin Kerschensteiner,
Mikael Simons,
Thomas Misgeld,
Martina Schifferer
Affiliations
Georg Kislinger
German Center for Neurodegenerative Diseases (DZNE), Munich 81377, Germany; Munich Cluster of Systems Neurology (SyNergy), Munich 81377, Germany; Institute of Neuronal Cell Biology, Technical University Munich, Munich 80802, Germany
Helmut Gnägi
Diatome SA, Helmstrasse 1, 2560 Nidau, Switzerland
Martin Kerschensteiner
Munich Cluster of Systems Neurology (SyNergy), Munich 81377, Germany; Institute of Clinical Neuroimmunology, University Hospital, Ludwig-Maximilians-University Munich, Planegg-Martinsried 82152, Germany; Biomedical Center (BMC), Faculty of Medicine, Ludwig-Maximilians-University Munich, Planegg-Martinsried 82152, Germany
Mikael Simons
German Center for Neurodegenerative Diseases (DZNE), Munich 81377, Germany; Munich Cluster of Systems Neurology (SyNergy), Munich 81377, Germany; Institute of Neuronal Cell Biology, Technical University Munich, Munich 80802, Germany
Thomas Misgeld
German Center for Neurodegenerative Diseases (DZNE), Munich 81377, Germany; Munich Cluster of Systems Neurology (SyNergy), Munich 81377, Germany; Institute of Neuronal Cell Biology, Technical University Munich, Munich 80802, Germany
Martina Schifferer
German Center for Neurodegenerative Diseases (DZNE), Munich 81377, Germany; Munich Cluster of Systems Neurology (SyNergy), Munich 81377, Germany; Corresponding author
Summary: Volume electron microscopy enables the ultrastructural analysis of biological tissue. Currently, the techniques involving ultramicrotomy (ATUM, ssTEM) allow large fields of view but afford only limited z-resolution, whereas ion beam-milling approaches (FIB-SEM) yield isotropic voxels but are restricted in volume size. Now we present a hybrid method, named ATUM-FIB, which combines the advantages of both approaches. ATUM-FIB is based on serial sectioning of tissue into “semithick” (2–10 μm) sections collected onto tape. Serial light and electron microscopy allows the identification of regions of interest that are then directly accessible for targeted FIB-SEM. The set of semithick sections thus represents a tissue “library” which provides three-dimensional context information that can be probed “on demand” by local high-resolution analysis. We demonstrate the potential of this technique to reveal the ultrastructure of rare but pathologically important events by identifying microglia contact sites with amyloid plaques in a mouse model of familial Alzheimer's disease.