Cargando…
Semi-intact ex vivo approach to investigate spinal somatosensory circuits
The somatosensory input that gives rise to the perceptions of pain, itch, cold and heat are initially integrated in the superficial dorsal horn of the spinal cord. Here, we describe a new approach to investigate these neural circuits in mouse. This semi-intact somatosensory preparation enables recor...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5214752/ https://www.ncbi.nlm.nih.gov/pubmed/27991851 http://dx.doi.org/10.7554/eLife.22866 |
_version_ | 1782491662488961024 |
---|---|
author | Hachisuka, Junichi Baumbauer, Kyle M Omori, Yu Snyder, Lindsey M Koerber, H Richard Ross, Sarah E |
author_facet | Hachisuka, Junichi Baumbauer, Kyle M Omori, Yu Snyder, Lindsey M Koerber, H Richard Ross, Sarah E |
author_sort | Hachisuka, Junichi |
collection | PubMed |
description | The somatosensory input that gives rise to the perceptions of pain, itch, cold and heat are initially integrated in the superficial dorsal horn of the spinal cord. Here, we describe a new approach to investigate these neural circuits in mouse. This semi-intact somatosensory preparation enables recording from spinal output neurons, while precisely controlling somatosensory input, and simultaneously manipulating specific populations of spinal interneurons. Our findings suggest that spinal interneurons show distinct temporal and spatial tuning properties. We also show that modality selectivity — mechanical, heat and cold — can be assessed in both retrogradely labeled spinoparabrachial projection neurons and genetically labeled spinal interneurons. Finally, we demonstrate that interneuron connectivity can be determined via optogenetic activation of specific interneuron subtypes. This new approach may facilitate key conceptual advances in our understanding of the spinal somatosensory circuits in health and disease. DOI: http://dx.doi.org/10.7554/eLife.22866.001 |
format | Online Article Text |
id | pubmed-5214752 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-52147522017-01-09 Semi-intact ex vivo approach to investigate spinal somatosensory circuits Hachisuka, Junichi Baumbauer, Kyle M Omori, Yu Snyder, Lindsey M Koerber, H Richard Ross, Sarah E eLife Neuroscience The somatosensory input that gives rise to the perceptions of pain, itch, cold and heat are initially integrated in the superficial dorsal horn of the spinal cord. Here, we describe a new approach to investigate these neural circuits in mouse. This semi-intact somatosensory preparation enables recording from spinal output neurons, while precisely controlling somatosensory input, and simultaneously manipulating specific populations of spinal interneurons. Our findings suggest that spinal interneurons show distinct temporal and spatial tuning properties. We also show that modality selectivity — mechanical, heat and cold — can be assessed in both retrogradely labeled spinoparabrachial projection neurons and genetically labeled spinal interneurons. Finally, we demonstrate that interneuron connectivity can be determined via optogenetic activation of specific interneuron subtypes. This new approach may facilitate key conceptual advances in our understanding of the spinal somatosensory circuits in health and disease. DOI: http://dx.doi.org/10.7554/eLife.22866.001 eLife Sciences Publications, Ltd 2016-12-19 /pmc/articles/PMC5214752/ /pubmed/27991851 http://dx.doi.org/10.7554/eLife.22866 Text en © 2016, Hachisuka et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Hachisuka, Junichi Baumbauer, Kyle M Omori, Yu Snyder, Lindsey M Koerber, H Richard Ross, Sarah E Semi-intact ex vivo approach to investigate spinal somatosensory circuits |
title | Semi-intact ex vivo approach to investigate spinal somatosensory circuits |
title_full | Semi-intact ex vivo approach to investigate spinal somatosensory circuits |
title_fullStr | Semi-intact ex vivo approach to investigate spinal somatosensory circuits |
title_full_unstemmed | Semi-intact ex vivo approach to investigate spinal somatosensory circuits |
title_short | Semi-intact ex vivo approach to investigate spinal somatosensory circuits |
title_sort | semi-intact ex vivo approach to investigate spinal somatosensory circuits |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5214752/ https://www.ncbi.nlm.nih.gov/pubmed/27991851 http://dx.doi.org/10.7554/eLife.22866 |
work_keys_str_mv | AT hachisukajunichi semiintactexvivoapproachtoinvestigatespinalsomatosensorycircuits AT baumbauerkylem semiintactexvivoapproachtoinvestigatespinalsomatosensorycircuits AT omoriyu semiintactexvivoapproachtoinvestigatespinalsomatosensorycircuits AT snyderlindseym semiintactexvivoapproachtoinvestigatespinalsomatosensorycircuits AT koerberhrichard semiintactexvivoapproachtoinvestigatespinalsomatosensorycircuits AT rosssarahe semiintactexvivoapproachtoinvestigatespinalsomatosensorycircuits |