Cargando…

Multiplex translaminar imaging in the spinal cord of behaving mice

While the spinal cord is known to play critical roles in sensorimotor processing, including pain-related signaling, corresponding activity patterns in genetically defined cell types across spinal laminae have remained challenging to investigate. Calcium imaging has enabled cellular activity measurem...

Descripción completa

Detalles Bibliográficos
Autores principales: Shekhtmeyster, Pavel, Carey, Erin M., Duarte, Daniela, Ngo, Alexander, Gao, Grace, Nelson, Nicholas A., Clark, Charles L., Nimmerjahn, Axel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10030868/
https://www.ncbi.nlm.nih.gov/pubmed/36944637
http://dx.doi.org/10.1038/s41467-023-36959-2
_version_ 1784910472363900928
author Shekhtmeyster, Pavel
Carey, Erin M.
Duarte, Daniela
Ngo, Alexander
Gao, Grace
Nelson, Nicholas A.
Clark, Charles L.
Nimmerjahn, Axel
author_facet Shekhtmeyster, Pavel
Carey, Erin M.
Duarte, Daniela
Ngo, Alexander
Gao, Grace
Nelson, Nicholas A.
Clark, Charles L.
Nimmerjahn, Axel
author_sort Shekhtmeyster, Pavel
collection PubMed
description While the spinal cord is known to play critical roles in sensorimotor processing, including pain-related signaling, corresponding activity patterns in genetically defined cell types across spinal laminae have remained challenging to investigate. Calcium imaging has enabled cellular activity measurements in behaving rodents but is currently limited to superficial regions. Here, using chronically implanted microprisms, we imaged sensory and motor-evoked activity in regions and at speeds inaccessible by other high-resolution imaging techniques. To enable translaminar imaging in freely behaving animals through implanted microprisms, we additionally developed wearable microscopes with custom-compound microlenses. This system addresses multiple challenges of previous wearable microscopes, including their limited working distance, resolution, contrast, and achromatic range. Using this system, we show that dorsal horn astrocytes in behaving mice show sensorimotor program-dependent and lamina-specific calcium excitation. Additionally, we show that tachykinin precursor 1 (Tac1)-expressing neurons exhibit translaminar activity to acute mechanical pain but not locomotion.
format Online
Article
Text
id pubmed-10030868
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-100308682023-03-23 Multiplex translaminar imaging in the spinal cord of behaving mice Shekhtmeyster, Pavel Carey, Erin M. Duarte, Daniela Ngo, Alexander Gao, Grace Nelson, Nicholas A. Clark, Charles L. Nimmerjahn, Axel Nat Commun Article While the spinal cord is known to play critical roles in sensorimotor processing, including pain-related signaling, corresponding activity patterns in genetically defined cell types across spinal laminae have remained challenging to investigate. Calcium imaging has enabled cellular activity measurements in behaving rodents but is currently limited to superficial regions. Here, using chronically implanted microprisms, we imaged sensory and motor-evoked activity in regions and at speeds inaccessible by other high-resolution imaging techniques. To enable translaminar imaging in freely behaving animals through implanted microprisms, we additionally developed wearable microscopes with custom-compound microlenses. This system addresses multiple challenges of previous wearable microscopes, including their limited working distance, resolution, contrast, and achromatic range. Using this system, we show that dorsal horn astrocytes in behaving mice show sensorimotor program-dependent and lamina-specific calcium excitation. Additionally, we show that tachykinin precursor 1 (Tac1)-expressing neurons exhibit translaminar activity to acute mechanical pain but not locomotion. Nature Publishing Group UK 2023-03-21 /pmc/articles/PMC10030868/ /pubmed/36944637 http://dx.doi.org/10.1038/s41467-023-36959-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Shekhtmeyster, Pavel
Carey, Erin M.
Duarte, Daniela
Ngo, Alexander
Gao, Grace
Nelson, Nicholas A.
Clark, Charles L.
Nimmerjahn, Axel
Multiplex translaminar imaging in the spinal cord of behaving mice
title Multiplex translaminar imaging in the spinal cord of behaving mice
title_full Multiplex translaminar imaging in the spinal cord of behaving mice
title_fullStr Multiplex translaminar imaging in the spinal cord of behaving mice
title_full_unstemmed Multiplex translaminar imaging in the spinal cord of behaving mice
title_short Multiplex translaminar imaging in the spinal cord of behaving mice
title_sort multiplex translaminar imaging in the spinal cord of behaving mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10030868/
https://www.ncbi.nlm.nih.gov/pubmed/36944637
http://dx.doi.org/10.1038/s41467-023-36959-2
work_keys_str_mv AT shekhtmeysterpavel multiplextranslaminarimaginginthespinalcordofbehavingmice
AT careyerinm multiplextranslaminarimaginginthespinalcordofbehavingmice
AT duartedaniela multiplextranslaminarimaginginthespinalcordofbehavingmice
AT ngoalexander multiplextranslaminarimaginginthespinalcordofbehavingmice
AT gaograce multiplextranslaminarimaginginthespinalcordofbehavingmice
AT nelsonnicholasa multiplextranslaminarimaginginthespinalcordofbehavingmice
AT clarkcharlesl multiplextranslaminarimaginginthespinalcordofbehavingmice
AT nimmerjahnaxel multiplextranslaminarimaginginthespinalcordofbehavingmice