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3D Imaging of Axons in Transparent Spinal Cords from Rodents and Nonhuman Primates1,2,3

The histological assessment of spinal cord tissue in three dimensions has previously been very time consuming and prone to errors of interpretation. Advances in tissue clearing have significantly improved visualization of fluorescently labelled axons. While recent proof-of-concept studies have been...

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Autores principales: Soderblom, Cynthia, Lee, Do-Hun, Dawood, Abdul, Carballosa, Melissa, Santamaria, Andrea Jimena, Benavides, Francisco D., Jergova, Stanislava, Grumbles, Robert M., Thomas, Christine K., Park, Kevin K., Guest, James David, Lemmon, Vance P., Lee, Jae K., Tsoulfas, Pantelis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4444235/
https://www.ncbi.nlm.nih.gov/pubmed/26023683
http://dx.doi.org/10.1523/ENEURO.0001-15.2015
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author Soderblom, Cynthia
Lee, Do-Hun
Dawood, Abdul
Carballosa, Melissa
Santamaria, Andrea Jimena
Benavides, Francisco D.
Jergova, Stanislava
Grumbles, Robert M.
Thomas, Christine K.
Park, Kevin K.
Guest, James David
Lemmon, Vance P.
Lee, Jae K.
Tsoulfas, Pantelis
author_facet Soderblom, Cynthia
Lee, Do-Hun
Dawood, Abdul
Carballosa, Melissa
Santamaria, Andrea Jimena
Benavides, Francisco D.
Jergova, Stanislava
Grumbles, Robert M.
Thomas, Christine K.
Park, Kevin K.
Guest, James David
Lemmon, Vance P.
Lee, Jae K.
Tsoulfas, Pantelis
author_sort Soderblom, Cynthia
collection PubMed
description The histological assessment of spinal cord tissue in three dimensions has previously been very time consuming and prone to errors of interpretation. Advances in tissue clearing have significantly improved visualization of fluorescently labelled axons. While recent proof-of-concept studies have been performed with transgenic mice in which axons were prelabeled with GFP, investigating axonal regeneration requires stringent axonal tracing methods as well as the use of animal models in which transgenic axonal labeling is not available. Using rodent models of spinal cord injury, we labeled axon tracts of interest using both adeno-associated virus and chemical tracers and performed tetrahydrofuran-based tissue clearing to image multiple axon types in spinal cords using light sheet and confocal microscopy. Using this approach, we investigated the relationships between axons and scar-forming cells at the injury site as well as connections between sensory axons and motor pools in the spinal cord. In addition, we used these methods to trace axons in nonhuman primates. This reproducible and adaptable virus-based approach can be combined with transgenic mice or with chemical-based tract-tracing methods, providing scientists with flexibility in obtaining axonal trajectory information from transparent tissue.
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spelling pubmed-44442352015-05-26 3D Imaging of Axons in Transparent Spinal Cords from Rodents and Nonhuman Primates1,2,3 Soderblom, Cynthia Lee, Do-Hun Dawood, Abdul Carballosa, Melissa Santamaria, Andrea Jimena Benavides, Francisco D. Jergova, Stanislava Grumbles, Robert M. Thomas, Christine K. Park, Kevin K. Guest, James David Lemmon, Vance P. Lee, Jae K. Tsoulfas, Pantelis eNeuro Methods/New Tools The histological assessment of spinal cord tissue in three dimensions has previously been very time consuming and prone to errors of interpretation. Advances in tissue clearing have significantly improved visualization of fluorescently labelled axons. While recent proof-of-concept studies have been performed with transgenic mice in which axons were prelabeled with GFP, investigating axonal regeneration requires stringent axonal tracing methods as well as the use of animal models in which transgenic axonal labeling is not available. Using rodent models of spinal cord injury, we labeled axon tracts of interest using both adeno-associated virus and chemical tracers and performed tetrahydrofuran-based tissue clearing to image multiple axon types in spinal cords using light sheet and confocal microscopy. Using this approach, we investigated the relationships between axons and scar-forming cells at the injury site as well as connections between sensory axons and motor pools in the spinal cord. In addition, we used these methods to trace axons in nonhuman primates. This reproducible and adaptable virus-based approach can be combined with transgenic mice or with chemical-based tract-tracing methods, providing scientists with flexibility in obtaining axonal trajectory information from transparent tissue. Society for Neuroscience 2015-04-08 /pmc/articles/PMC4444235/ /pubmed/26023683 http://dx.doi.org/10.1523/ENEURO.0001-15.2015 Text en Copyright © 2015 Soderblom et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Methods/New Tools
Soderblom, Cynthia
Lee, Do-Hun
Dawood, Abdul
Carballosa, Melissa
Santamaria, Andrea Jimena
Benavides, Francisco D.
Jergova, Stanislava
Grumbles, Robert M.
Thomas, Christine K.
Park, Kevin K.
Guest, James David
Lemmon, Vance P.
Lee, Jae K.
Tsoulfas, Pantelis
3D Imaging of Axons in Transparent Spinal Cords from Rodents and Nonhuman Primates1,2,3
title 3D Imaging of Axons in Transparent Spinal Cords from Rodents and Nonhuman Primates1,2,3
title_full 3D Imaging of Axons in Transparent Spinal Cords from Rodents and Nonhuman Primates1,2,3
title_fullStr 3D Imaging of Axons in Transparent Spinal Cords from Rodents and Nonhuman Primates1,2,3
title_full_unstemmed 3D Imaging of Axons in Transparent Spinal Cords from Rodents and Nonhuman Primates1,2,3
title_short 3D Imaging of Axons in Transparent Spinal Cords from Rodents and Nonhuman Primates1,2,3
title_sort 3d imaging of axons in transparent spinal cords from rodents and nonhuman primates1,2,3
topic Methods/New Tools
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4444235/
https://www.ncbi.nlm.nih.gov/pubmed/26023683
http://dx.doi.org/10.1523/ENEURO.0001-15.2015
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