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Biology subjects

Fontenas, L.

Publications and source records attributed to Fontenas, L..

3 recordsLinked to original sources

Astrocytic Signatures in Neuronal Activity: A Machine Learning-Based Identification Approach

This study investigates the expanding role of astrocytes, the predominant glial cells, in brain function, focusing on whether and how their presence influences neuronal network activity. We focus on particular network activities identified as synchronous and asynchronous. Using computational modeling to generate synthetic data, we examine these network states and find that astrocytes significantly affect synaptic communication, mainly in synchronous states. We use different methods of extracting data from a network and compare which is best for identifying glial cells, with mean firing rate emerging with higher accuracy. To reach the aforementioned conclusions, we applied various machine learning techniques, including Decision Trees, Random Forests, Bagging, Gradient Boosting, and Feedforward Neural Networks, the latter outperforming other models. Our findings reveal that glial cells play a crucial role in modulating synaptic activity, especially in synchronous networks, highlighting potential avenues for their detection with machine learning models through experimental accessible measures.

neuroscience↗

Met is required for oligodendrocyte progenitor cell migration in Danio rerio

During vertebrate central nervous system development, most oligodendrocyte progenitor cells (OPCs) are specified in the ventral spinal cord and must migrate throughout the neural tube until they become evenly distributed, occupying non-overlapping domains. While this process of developmental OPC migration is well characterized, the nature of the molecular mediators that govern it remain largely unknown. Here, using zebrafish as a model, we demonstrate that Met signaling is required for initial developmental migration of OPCs, and, using cell-specific knock-down of Met signaling, show that Met acts cell-autonomously in OPCs. Taken together, these findings demonstrate in vivo, the role of Met signaling in OPC migration and provide new insight into how OPC migration is regulated during development.

neuroscience↗

Spinal cord precursors utilize neural crest cell mechanisms to generate hybrid peripheral myelinating glia

During development, oligodendrocytes and Schwann cells myelinate central and peripheral nervous system axons, respectively, while motor exit point (MEP) glia are neural tube-derived, peripheral glia that myelinate axonal territory between these populations at MEP transition zones. From which specific neural tube precursors MEP glia are specified, and how they exit the neural tube to migrate onto peripheral motor axons, remain largely unknown. Here, using zebrafish, we found that MEP glia arise from lateral floor plate precursors and require foxd3 to delaminate and exit the spinal cord. Additionally, we show that similar to Schwann cells, MEP glial development depends on axonally-derived neuregulin1. Finally, our data demonstrate that overexpressing axonal cues is sufficient to generate additional MEP glia in the spinal cord. Overall, these studies provide new insight into how a novel population of hybrid, peripheral myelinating glia are generated from neural tube precursors and migrate into the periphery.

developmental biology↗