Cargando…
Noise Normalizes Firing Output of Mouse Lateral Geniculate Nucleus Neurons
The output of individual neurons is dependent on both synaptic and intrinsic membrane properties. While it is clear that the response of an individual neuron can be facilitated or inhibited based on the summation of its constituent synaptic inputs, it is not clear whether subthreshold activity, (e.g...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3585224/ https://www.ncbi.nlm.nih.gov/pubmed/23469120 http://dx.doi.org/10.1371/journal.pone.0057961 |
_version_ | 1782261124022927360 |
---|---|
author | Wijesinghe, Rajiv Solomon, Samuel G. Camp, Aaron J. |
author_facet | Wijesinghe, Rajiv Solomon, Samuel G. Camp, Aaron J. |
author_sort | Wijesinghe, Rajiv |
collection | PubMed |
description | The output of individual neurons is dependent on both synaptic and intrinsic membrane properties. While it is clear that the response of an individual neuron can be facilitated or inhibited based on the summation of its constituent synaptic inputs, it is not clear whether subthreshold activity, (e.g. synaptic “noise”- fluctuations that do not change the mean membrane potential) also serve a function in the control of neuronal output. Here we studied this by making whole-cell patch-clamp recordings from 29 mouse thalamocortical relay (TC) neurons. For each neuron we measured neuronal gain in response to either injection of current noise, or activation of the metabotropic glutamate receptor-mediated cortical feedback network (synaptic noise). As expected, injection of current noise via the recording pipette induces shifts in neuronal gain that are dependent on the amplitude of current noise, such that larger shifts in gain are observed in response to larger amplitude noise injections. Importantly we show that shifts in neuronal gain are also dependent on the intrinsic sensitivity of the neuron tested, such that the gain of intrinsically sensitive neurons is attenuated divisively in response to current noise, while the gain of insensitive neurons is facilitated multiplicatively by injection of current noise- effectively normalizing the output of the dLGN as a whole. In contrast, when the cortical feedback network was activated, only multiplicative gain changes were observed. These network activation-dependent changes were associated with reductions in the slow afterhyperpolarization (sAHP), and were mediated at least in part, by T-type calcium channels. Together, this suggests that TC neurons have the machinery necessary to compute multiple output solutions to a given set of stimuli depending on the current level of network stimulation. |
format | Online Article Text |
id | pubmed-3585224 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-35852242013-03-06 Noise Normalizes Firing Output of Mouse Lateral Geniculate Nucleus Neurons Wijesinghe, Rajiv Solomon, Samuel G. Camp, Aaron J. PLoS One Research Article The output of individual neurons is dependent on both synaptic and intrinsic membrane properties. While it is clear that the response of an individual neuron can be facilitated or inhibited based on the summation of its constituent synaptic inputs, it is not clear whether subthreshold activity, (e.g. synaptic “noise”- fluctuations that do not change the mean membrane potential) also serve a function in the control of neuronal output. Here we studied this by making whole-cell patch-clamp recordings from 29 mouse thalamocortical relay (TC) neurons. For each neuron we measured neuronal gain in response to either injection of current noise, or activation of the metabotropic glutamate receptor-mediated cortical feedback network (synaptic noise). As expected, injection of current noise via the recording pipette induces shifts in neuronal gain that are dependent on the amplitude of current noise, such that larger shifts in gain are observed in response to larger amplitude noise injections. Importantly we show that shifts in neuronal gain are also dependent on the intrinsic sensitivity of the neuron tested, such that the gain of intrinsically sensitive neurons is attenuated divisively in response to current noise, while the gain of insensitive neurons is facilitated multiplicatively by injection of current noise- effectively normalizing the output of the dLGN as a whole. In contrast, when the cortical feedback network was activated, only multiplicative gain changes were observed. These network activation-dependent changes were associated with reductions in the slow afterhyperpolarization (sAHP), and were mediated at least in part, by T-type calcium channels. Together, this suggests that TC neurons have the machinery necessary to compute multiple output solutions to a given set of stimuli depending on the current level of network stimulation. Public Library of Science 2013-02-28 /pmc/articles/PMC3585224/ /pubmed/23469120 http://dx.doi.org/10.1371/journal.pone.0057961 Text en © 2013 Wijesinghe et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Wijesinghe, Rajiv Solomon, Samuel G. Camp, Aaron J. Noise Normalizes Firing Output of Mouse Lateral Geniculate Nucleus Neurons |
title | Noise Normalizes Firing Output of Mouse Lateral Geniculate Nucleus Neurons |
title_full | Noise Normalizes Firing Output of Mouse Lateral Geniculate Nucleus Neurons |
title_fullStr | Noise Normalizes Firing Output of Mouse Lateral Geniculate Nucleus Neurons |
title_full_unstemmed | Noise Normalizes Firing Output of Mouse Lateral Geniculate Nucleus Neurons |
title_short | Noise Normalizes Firing Output of Mouse Lateral Geniculate Nucleus Neurons |
title_sort | noise normalizes firing output of mouse lateral geniculate nucleus neurons |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3585224/ https://www.ncbi.nlm.nih.gov/pubmed/23469120 http://dx.doi.org/10.1371/journal.pone.0057961 |
work_keys_str_mv | AT wijesingherajiv noisenormalizesfiringoutputofmouselateralgeniculatenucleusneurons AT solomonsamuelg noisenormalizesfiringoutputofmouselateralgeniculatenucleusneurons AT campaaronj noisenormalizesfiringoutputofmouselateralgeniculatenucleusneurons |