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Protocol to correlate electron microscopy with electrophysiology in single-cell autaptic microcultures. | LitMetric

Protocol to correlate electron microscopy with electrophysiology in single-cell autaptic microcultures.

STAR Protoc

Laboratory of Neurobiology, Department of Pathology and Experimental Therapy, Institute of Neurosciences, University of Barcelona, L'Hospitalet de Llobregat, 08907 Barcelona, Spain; Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, 08907 Barcelona, Spain. Electronic address:

Published: June 2024

AI Article Synopsis

Article Abstract

Single-cell microcultures (SCMs) form a monosynaptic circuit that allows stimulation and recording of postsynaptic responses using a single electrode. Here, we present a protocol to establish autaptic cultures from rat superior cervical ganglion neurons. We describe the steps for preparing SCMs, recording synaptic currents, and identifying and processing the recorded neurons for electron microscopy. We then detail procedures for visualizing synapses. This protocol is illustrated by correlating evoked and spontaneous neurotransmitter release with the ultrastructural features of synapses recorded. For complete details on the use and execution of this protocol, please refer to Velasco et al..

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11101974PMC
http://dx.doi.org/10.1016/j.xpro.2024.103003DOI Listing

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