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Non-synaptic Plasticity in Leech Touch Cells
The role of Na(+)/K(+)-pumps in activity-dependent synaptic plasticity has been described in both vertebrates and invertebrates. Here, we provide evidence that the Na(+)/K(+)-pump is also involved in activity-dependent non-synaptic cellular plasticity in leech sensory neurons. We show that the resti...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6890822/ https://www.ncbi.nlm.nih.gov/pubmed/31827443 http://dx.doi.org/10.3389/fphys.2019.01444 |
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author | Meiser, Sonja Ashida, Go Kretzberg, Jutta |
author_facet | Meiser, Sonja Ashida, Go Kretzberg, Jutta |
author_sort | Meiser, Sonja |
collection | PubMed |
description | The role of Na(+)/K(+)-pumps in activity-dependent synaptic plasticity has been described in both vertebrates and invertebrates. Here, we provide evidence that the Na(+)/K(+)-pump is also involved in activity-dependent non-synaptic cellular plasticity in leech sensory neurons. We show that the resting membrane potential (RMP) of T cells hyperpolarizes in response to repeated somatic current injection, while at the same time their spike count (SC) and the input resistance (IR) increase. Our Hodgkin–Huxley-type neuron model, adjusted to physiological T cell properties, suggests that repetitive action potential discharges lead to increased Na(+)/K(+)-pump activity, which then hyperpolarizes the RMP. In consequence, a slow, non-inactivating current decreases, which is presumably mediated by voltage-dependent, low-threshold potassium channels. Closing of these putative M-type channels due to hyperpolarization of the resting potential increases the IR of the cell, leading to a larger number of spikes. By this mechanism, the response behavior switches from rapidly to slowly adapting spiking. These changes in spiking behavior also effect other T cells on the same side of the ganglion, which are connected via a combination of electrical and chemical synapses. An increased SC in the presynaptic T cell results in larger postsynaptic responses (PRs) in the other T cells. However, when the number of elicited presynaptic spikes is kept constant, the PR does not change. These results suggest that T cells change their responses in an activity-dependent manner through non-synaptic rather than synaptic plasticity. These changes might act as a gain-control mechanism. Depending on the previous activity, this gain could scale the relative impacts of synaptic inputs from other mechanoreceptors, versus the spike responses to tactile skin stimulation. This multi-tasking ability, and its flexible adaptation to previous activity, might make the T cell a key player in a preparatory network, enabling the leech to perform fast behavioral reactions to skin stimulation. |
format | Online Article Text |
id | pubmed-6890822 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68908222019-12-11 Non-synaptic Plasticity in Leech Touch Cells Meiser, Sonja Ashida, Go Kretzberg, Jutta Front Physiol Physiology The role of Na(+)/K(+)-pumps in activity-dependent synaptic plasticity has been described in both vertebrates and invertebrates. Here, we provide evidence that the Na(+)/K(+)-pump is also involved in activity-dependent non-synaptic cellular plasticity in leech sensory neurons. We show that the resting membrane potential (RMP) of T cells hyperpolarizes in response to repeated somatic current injection, while at the same time their spike count (SC) and the input resistance (IR) increase. Our Hodgkin–Huxley-type neuron model, adjusted to physiological T cell properties, suggests that repetitive action potential discharges lead to increased Na(+)/K(+)-pump activity, which then hyperpolarizes the RMP. In consequence, a slow, non-inactivating current decreases, which is presumably mediated by voltage-dependent, low-threshold potassium channels. Closing of these putative M-type channels due to hyperpolarization of the resting potential increases the IR of the cell, leading to a larger number of spikes. By this mechanism, the response behavior switches from rapidly to slowly adapting spiking. These changes in spiking behavior also effect other T cells on the same side of the ganglion, which are connected via a combination of electrical and chemical synapses. An increased SC in the presynaptic T cell results in larger postsynaptic responses (PRs) in the other T cells. However, when the number of elicited presynaptic spikes is kept constant, the PR does not change. These results suggest that T cells change their responses in an activity-dependent manner through non-synaptic rather than synaptic plasticity. These changes might act as a gain-control mechanism. Depending on the previous activity, this gain could scale the relative impacts of synaptic inputs from other mechanoreceptors, versus the spike responses to tactile skin stimulation. This multi-tasking ability, and its flexible adaptation to previous activity, might make the T cell a key player in a preparatory network, enabling the leech to perform fast behavioral reactions to skin stimulation. Frontiers Media S.A. 2019-11-27 /pmc/articles/PMC6890822/ /pubmed/31827443 http://dx.doi.org/10.3389/fphys.2019.01444 Text en Copyright © 2019 Meiser, Ashida and Kretzberg. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology Meiser, Sonja Ashida, Go Kretzberg, Jutta Non-synaptic Plasticity in Leech Touch Cells |
title | Non-synaptic Plasticity in Leech Touch Cells |
title_full | Non-synaptic Plasticity in Leech Touch Cells |
title_fullStr | Non-synaptic Plasticity in Leech Touch Cells |
title_full_unstemmed | Non-synaptic Plasticity in Leech Touch Cells |
title_short | Non-synaptic Plasticity in Leech Touch Cells |
title_sort | non-synaptic plasticity in leech touch cells |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6890822/ https://www.ncbi.nlm.nih.gov/pubmed/31827443 http://dx.doi.org/10.3389/fphys.2019.01444 |
work_keys_str_mv | AT meisersonja nonsynapticplasticityinleechtouchcells AT ashidago nonsynapticplasticityinleechtouchcells AT kretzbergjutta nonsynapticplasticityinleechtouchcells |