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Meral, E. S.

Publications and source records attributed to Meral, E. S..

2 recordsLinked to original sources

Structured Sampling of Molecularly Classified Mossy Fiber Inputs by Cerebellar Granule Cells

The cerebellar granule cell layer receives mossy fiber inputs from diverse brain regions, yet the principles governing how individual granule cells sample distinct types of inputs remain poorly understood. Using a volumetric correlated light and electron microscopy (vCLEM) dataset from an adult female mouse cerebellum, in which VGluT1-positive and VGluT1-negative mossy fiber terminals are molecularly distinguished, we reconstructed granule cell and mossy fiber connectivity to examine input selection rules. We constructed spatially constrained null models to simulate sampling during adulthood and development. Granule cell-centered analysis showed that granule cells shared less innervation from the same mossy fiber than expected by chance. Moreover, subpopulations of granule cells preferentially sample either VGluT1-positive or VGluT1-negative mossy fibers. In contrast, mossy fiber-centered analysis showed that individual terminals distributed their outputs across granule cells in a pattern consistent with random sampling. However, sampling in the adult state was more selective than in developmental simulations. Together, our findings demonstrated structured, non-random sampling of cerebellar VGluT1-positive and VGluT1-negative mossy fiber inputs and provide a framework for understanding how granule cells integrate molecularly distinct inputs to support cerebellar computation.

neuroscience↗

Multiplexed Volumetric CLEM enabled by antibody derivatives provides new insights into the cytology of the mouse cerebellar cortex

Mapping neuronal networks that underlie behavior has become a central focus in neuroscience. While serial section electron microscopy (ssEM) can reveal the fine structure of neuronal networks (connectomics), it does not provide the molecular information that helps identify cell types or their functional properties. Volumetric correlated light and electron microscopy (vCLEM) combines ssEM and volumetric fluorescence microscopy to incorporate molecular labeling into ssEM datasets. We developed an approach that uses small fluorescent single-chain variable fragment (scFv) immuno-probes to perform multiplexed detergent-free immuno-labeling and ssEM on the same samples. We generated eight such fluorescent scFvs that targeted useful markers for brain studies (green fluorescent protein, glial fibrillary acidic protein, calbindin, parvalbumin, voltage-gated potassium channel subfamily A member 2, vesicular glutamate transporter 1, postsynaptic density protein 95, and neuropeptide Y). To test the vCLEM approach, six different fluorescent probes were imaged in a sample of the cortex of a cerebellar lobule (Crus 1), using confocal microscopy with spectral unmixing, followed by ssEM imaging of the same sample. The results show excellent ultrastructure with superimposition of the multiple fluorescence channels. Using this approach we could document a poorly described cell type in the cerebellum, two types of mossy fiber terminals, and the subcellular localization of one type of ion channel. Because scFvs can be derived from existing monoclonal antibodies, hundreds of such probes can be generated to enable molecular overlays for connectomic studies.

neuroscience↗