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Diversified physiological sensory input connectivity questions the existence of distinct classes of spinal interneurons
The spinal cord is engaged in all forms of motor performance but its functions are far from understood. Because network connectivity defines function, we explored the connectivity of muscular, tendon, and tactile sensory inputs among a wide population of spinal interneurons in the lower cervical seg...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8971951/ https://www.ncbi.nlm.nih.gov/pubmed/35372805 http://dx.doi.org/10.1016/j.isci.2022.104083 |
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author | Kohler, Matthias Bengtsson, Fredrik Stratmann, Philipp Röhrbein, Florian Knoll, Alois Albu-Schäffer, Alin Jörntell, Henrik |
author_facet | Kohler, Matthias Bengtsson, Fredrik Stratmann, Philipp Röhrbein, Florian Knoll, Alois Albu-Schäffer, Alin Jörntell, Henrik |
author_sort | Kohler, Matthias |
collection | PubMed |
description | The spinal cord is engaged in all forms of motor performance but its functions are far from understood. Because network connectivity defines function, we explored the connectivity of muscular, tendon, and tactile sensory inputs among a wide population of spinal interneurons in the lower cervical segments. Using low noise intracellular whole cell recordings in the decerebrated, non-anesthetized cat in vivo, we could define mono-, di-, and trisynaptic inputs as well as the weights of each input. Whereas each neuron had a highly specific input, and each indirect input could moreover be explained by inputs in other recorded neurons, we unexpectedly also found the input connectivity of the spinal interneuron population to form a continuum. Our data hence contrasts with the currently widespread notion of distinct classes of interneurons. We argue that this suggested diversified physiological connectivity, which likely requires a major component of circuitry learning, implies a more flexible functionality. |
format | Online Article Text |
id | pubmed-8971951 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-89719512022-04-02 Diversified physiological sensory input connectivity questions the existence of distinct classes of spinal interneurons Kohler, Matthias Bengtsson, Fredrik Stratmann, Philipp Röhrbein, Florian Knoll, Alois Albu-Schäffer, Alin Jörntell, Henrik iScience Article The spinal cord is engaged in all forms of motor performance but its functions are far from understood. Because network connectivity defines function, we explored the connectivity of muscular, tendon, and tactile sensory inputs among a wide population of spinal interneurons in the lower cervical segments. Using low noise intracellular whole cell recordings in the decerebrated, non-anesthetized cat in vivo, we could define mono-, di-, and trisynaptic inputs as well as the weights of each input. Whereas each neuron had a highly specific input, and each indirect input could moreover be explained by inputs in other recorded neurons, we unexpectedly also found the input connectivity of the spinal interneuron population to form a continuum. Our data hence contrasts with the currently widespread notion of distinct classes of interneurons. We argue that this suggested diversified physiological connectivity, which likely requires a major component of circuitry learning, implies a more flexible functionality. Elsevier 2022-03-17 /pmc/articles/PMC8971951/ /pubmed/35372805 http://dx.doi.org/10.1016/j.isci.2022.104083 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Kohler, Matthias Bengtsson, Fredrik Stratmann, Philipp Röhrbein, Florian Knoll, Alois Albu-Schäffer, Alin Jörntell, Henrik Diversified physiological sensory input connectivity questions the existence of distinct classes of spinal interneurons |
title | Diversified physiological sensory input connectivity questions the existence of distinct classes of spinal interneurons |
title_full | Diversified physiological sensory input connectivity questions the existence of distinct classes of spinal interneurons |
title_fullStr | Diversified physiological sensory input connectivity questions the existence of distinct classes of spinal interneurons |
title_full_unstemmed | Diversified physiological sensory input connectivity questions the existence of distinct classes of spinal interneurons |
title_short | Diversified physiological sensory input connectivity questions the existence of distinct classes of spinal interneurons |
title_sort | diversified physiological sensory input connectivity questions the existence of distinct classes of spinal interneurons |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8971951/ https://www.ncbi.nlm.nih.gov/pubmed/35372805 http://dx.doi.org/10.1016/j.isci.2022.104083 |
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