Reconstruction of genetically identified neurons imaged by serial-section electron microscopy
Maximilian Joesch,
David Mankus,
Masahito Yamagata,
Ali Shahbazi,
Richard Schalek,
Adi Suissa-Peleg,
Markus Meister,
Jeff W Lichtman,
Walter J Scheirer,
Joshua R Sanes
Affiliations
Maximilian Joesch
Center for Brain Science, Harvard University, Cambridge, United States; Department of Molecular and Cellular Biology, Harvard University, Cambridge, United States
David Mankus
Center for Brain Science, Harvard University, Cambridge, United States; Department of Molecular and Cellular Biology, Harvard University, Cambridge, United States
Center for Brain Science, Harvard University, Cambridge, United States; Department of Molecular and Cellular Biology, Harvard University, Cambridge, United States
Ali Shahbazi
University of Notre Dame, Notre Dame, United States
Richard Schalek
Center for Brain Science, Harvard University, Cambridge, United States; Department of Molecular and Cellular Biology, Harvard University, Cambridge, United States
Adi Suissa-Peleg
School of Engineering and Applied Sciences, Harvard University, Cambridge, United States
Division of Biology, California Institute of Technology, Pasadena, United States
Jeff W Lichtman
Center for Brain Science, Harvard University, Cambridge, United States; Department of Molecular and Cellular Biology, Harvard University, Cambridge, United States
Walter J Scheirer
University of Notre Dame, Notre Dame, United States
Center for Brain Science, Harvard University, Cambridge, United States; Department of Molecular and Cellular Biology, Harvard University, Cambridge, United States
Resolving patterns of synaptic connectivity in neural circuits currently requires serial section electron microscopy. However, complete circuit reconstruction is prohibitively slow and may not be necessary for many purposes such as comparing neuronal structure and connectivity among multiple animals. Here, we present an alternative strategy, targeted reconstruction of specific neuronal types. We used viral vectors to deliver peroxidase derivatives, which catalyze production of an electron-dense tracer, to genetically identify neurons, and developed a protocol that enhances the electron-density of the labeled cells while retaining the quality of the ultrastructure. The high contrast of the marked neurons enabled two innovations that speed data acquisition: targeted high-resolution reimaging of regions selected from rapidly-acquired lower resolution reconstruction, and an unsupervised segmentation algorithm. This pipeline reduces imaging and reconstruction times by two orders of magnitude, facilitating directed inquiry of circuit motifs.