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Sorokina, A.

Publications and source records attributed to Sorokina, A..

2 recordsLinked to original sources

Local Dendritic Landscape of Mouse V1

The principles that govern where excitatory synapses form on cortical pyramidal neurons remain unclear. A long-standing hypothesis is that connectivity mirrors neuronal geometry--with apical dendrites dominating in layer 1 and basal dendrites in deeper layers. Leveraging the MiCRONS cubic-millimetre serial electron-microscopy dataset ([1, 2]), we mapped 4968 synapses onto reconstructed apical and basal arbors across layers 1-6 of mouse visual cortex. Contrary to a simple gradient model, synaptic targeting is overwhelmingly biased toward basal dendrites in layers 2/3-6, even where apical shafts are abundant. Layer 1 is the sole exception, exhibiting the expected apical bias. Basal predominance scales with local soma density and the relative arbor length available for contact, such that 66% (61101/92445) of all synapses land within 130 {micro}m of the soma, placing most excitatory drive near the cell body. Axonal analysis revealed specificity beyond mere geometric opportunity: individual axon segments preferentially innervated either basal or apical compartments far more often than predicted by chance, indicating compartment-selective wiring rules. Together, our results show that cortical connectivity is shaped by both neuronal geometry and axon-level targeting preferences, redefining how pyramidal cells integrate information across layers and apical and basal dendrites.

neuroscience↗

Multi-modal imaging of a single postmortem mouse brain over five orders of magnitude of resolution

Mammalian neurons operate at length scales spanning five orders of magnitude; micron-scale-diameter myelinated axons project millimeters across brain regions, ultimately forming nanometer scale synapses on individual post-synaptic neurons. Capturing these anatomical features across that breadth of scale has required imaging samples with multiple independent imaging modalities (e.g. MRI, electron microscopy, etc.). Translating between the different modalities, however, requires imaging the same brain with each. Here, we imaged the same postmortem mouse brain over five orders of spatial resolution using MRI, whole brain micron-scale synchrotron x-ray tomography (CT), and large volume automated serial electron microscopy. Using this pipeline, we can track individual myelinated axons previously relegated to axon bundles in diffusion tensor MRI or arbitrarily trace neurons and their processes brain-wide and identify individual synapses on them. This pipeline provides both an unprecedented look across a single brains multi-scaled organization as well as a vehicle for studying the brains multi-scale pathologies.

neuroscience↗