AI Article Synopsis

  • Researchers tackled the challenges of mapping large primate brains by combining advanced tissue preparation techniques with ultra-fast fluorescence microscopy, achieving detailed whole-brain imaging in just 100 hours.
  • They created an innovative method called SMART (serial sectioning and clearing, three-dimensional microscopy with semiautomated reconstruction and tracing) to handle massive datasets and map neural connections effectively.
  • With SMART, the team successfully generated a cortical projection map of the thalamus and observed unique patterns in axon routing within the brain's cortical regions.

Article Abstract

Whole-brain mesoscale mapping in primates has been hindered by large brain sizes and the relatively low throughput of available microscopy methods. Here, we present an approach that combines primate-optimized tissue sectioning and clearing with ultrahigh-speed fluorescence microscopy implementing improved volumetric imaging with synchronized on-the-fly-scan and readout technique, and is capable of completing whole-brain imaging of a rhesus monkey at 1 × 1 × 2.5 µm voxel resolution within 100 h. We also developed a highly efficient method for long-range tracing of sparse axonal fibers in datasets numbering hundreds of terabytes. This pipeline, which we call serial sectioning and clearing, three-dimensional microscopy with semiautomated reconstruction and tracing (SMART), enables effective connectome-scale mapping of large primate brains. With SMART, we were able to construct a cortical projection map of the mediodorsal nucleus of the thalamus and identify distinct turning and routing patterns of individual axons in the cortical folds while approaching their arborization destinations.

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Source
http://dx.doi.org/10.1038/s41587-021-00986-5DOI Listing

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