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Advisor(s)
Abstract(s)
Objective. Recent technological advances are revealing the complex physiology of the axon and
challenging long-standing assumptions. Namely, while most action potential (AP) initiation occurs
at the axon initial segment in central nervous system neurons, initiation in distal parts of the axon
has been reported to occur in both physiological and pathological conditions. The functional role
of these ectopic APs, if exists, is still not clear, nor its impact on network activity dynamics.
Approach. Using an electrophysiology platform specifically designed for assessing axonal
conduction we show here for the first time regular and effective bidirectional axonal conduction in
hippocampal and dorsal root ganglia cultures. We investigate and characterize this bidirectional
propagation both in physiological conditions and after distal axotomy. Main results. A significant
fraction of APs are not coming from the canonical synapse-dendrite-soma signal flow, but instead
from signals originating at the distal axon. Importantly, antidromic APs may carry information
and can have a functional impact on the neuron, as they consistently depolarize the soma. Thus,
plasticity or gene transduction mechanisms triggered by soma depolarization can also be affected
by these antidromic APs. Conduction velocity is asymmetrical, with antidromic conduction being
slower than orthodromic. Significance. Altogether these findings have important implications for
the study of neuronal function in vitro, reshaping our understanding on how information flows in
neuronal cultures.
Description
Keywords
Microfluidics Microelectrode array Dorsal root ganglia Hippocampal neurons Ectopic action potential Bidirectional axonal conduction Axonal electrophysiology
Pedagogical Context
Citation
Mateus JC, Lopes C, Aroso M, Costa AR, Gerós A, Meneses J, Faria P, Neto E, Lamghari M, Sousa MM, Aguiar P. Bidirectional flow of action potentials in axons drives activity dynamics in neuronal cultures. J Neural Eng. 2021 Dec 29;18(6). doi: 10.1088/1741-2552/ac41db. PMID: 34891149
Publisher
IOP