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Graded spikes differentially signal neurotransmitter input in cerebrospinal fluid contacting neurons of the mouse spinal cord

The action potential and its all-or-none nature is fundamental to neural communication. Canonically, the action potential is initiated once voltage-activated Na(+) channels are activated, and their rapid kinetics of activation and inactivation give rise to the action potential’s all-or-none nature....

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Detalles Bibliográficos
Autores principales: Johnson, Emily, Clark, Marilyn, Oncul, Merve, Pantiru, Andreea, MacLean, Claudia, Deuchars, Jim, Deuchars, Susan A., Johnston, Jamie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9860393/
https://www.ncbi.nlm.nih.gov/pubmed/36691620
http://dx.doi.org/10.1016/j.isci.2022.105914
Descripción
Sumario:The action potential and its all-or-none nature is fundamental to neural communication. Canonically, the action potential is initiated once voltage-activated Na(+) channels are activated, and their rapid kinetics of activation and inactivation give rise to the action potential’s all-or-none nature. Here we demonstrate that cerebrospinal fluid contacting neurons (CSFcNs) surrounding the central canal of the mouse spinal cord employ a different strategy. Rather than using voltage-activated Na(+) channels to generate binary spikes, CSFcNs use two different types of voltage-activated Ca(2+) channel, enabling spikes of different amplitude. T-type Ca(2+) channels generate small amplitude spikes, whereas larger amplitude spikes require high voltage-activated Cd(2+)-sensitive Ca(2+) channels. We demonstrate that these different amplitude spikes can signal input from different transmitter systems; purinergic inputs evoke smaller T-type dependent spikes whereas cholinergic inputs evoke larger spikes that do not rely on T-type channels. Different synaptic inputs to CSFcNs can therefore be signaled by the spike amplitude.