Cargando…

Comprehensive Evaluation of Peripheral Nerve Regeneration in the Acute Healing Phase Using Tissue Clearing and Optical Microscopy in a Rodent Model

Peripheral nerve injury (PNI), a common injury in both the civilian and military arenas, is usually associated with high healthcare costs and with patients enduring slow recovery times, diminished quality of life, and potential long-term disability. Patients with PNI typically undergo complex interv...

Descripción completa

Detalles Bibliográficos
Autores principales: Jung, Yookyung, Ng, Joanna H., Keating, Cameron P., Senthil-Kumar, Prabhu, Zhao, Jie, Randolph, Mark A., Winograd, Jonathan M., Evans, Conor L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3979924/
https://www.ncbi.nlm.nih.gov/pubmed/24714405
http://dx.doi.org/10.1371/journal.pone.0094054
_version_ 1782310784685047808
author Jung, Yookyung
Ng, Joanna H.
Keating, Cameron P.
Senthil-Kumar, Prabhu
Zhao, Jie
Randolph, Mark A.
Winograd, Jonathan M.
Evans, Conor L.
author_facet Jung, Yookyung
Ng, Joanna H.
Keating, Cameron P.
Senthil-Kumar, Prabhu
Zhao, Jie
Randolph, Mark A.
Winograd, Jonathan M.
Evans, Conor L.
author_sort Jung, Yookyung
collection PubMed
description Peripheral nerve injury (PNI), a common injury in both the civilian and military arenas, is usually associated with high healthcare costs and with patients enduring slow recovery times, diminished quality of life, and potential long-term disability. Patients with PNI typically undergo complex interventions but the factors that govern optimal response are not fully characterized. A fundamental understanding of the cellular and tissue-level events in the immediate postoperative period is essential for improving treatment and optimizing repair. Here, we demonstrate a comprehensive imaging approach to evaluate peripheral nerve axonal regeneration in a rodent PNI model using a tissue clearing method to improve depth penetration while preserving neural architecture. Sciatic nerve transaction and end-to-end repair were performed in both wild type and thy-1 GFP rats. The nerves were harvested at time points after repair before undergoing whole mount immunofluorescence staining and tissue clearing. By increasing the optic depth penetration, tissue clearing allowed the visualization and evaluation of Wallerian degeneration and nerve regrowth throughout entire sciatic nerves with subcellular resolution. The tissue clearing protocol did not affect immunofluorescence labeling and no observable decrease in the fluorescence signal was observed. Large-area, high-resolution tissue volumes could be quantified to provide structural and connectivity information not available from current gold-standard approaches for evaluating axonal regeneration following PNI. The results are suggestive of observed behavioral recovery in vivo after neurorrhaphy, providing a method of evaluating axonal regeneration following repair that can serve as an adjunct to current standard outcomes measurements. This study demonstrates that tissue clearing following whole mount immunofluorescence staining enables the complete visualization and quantitative evaluation of axons throughout nerves in a PNI model. The methods developed in this study could advance PNI research allowing both researchers and clinicians to further understand the individual events of axonal degeneration and regeneration on a multifaceted level.
format Online
Article
Text
id pubmed-3979924
institution National Center for Biotechnology Information
language English
publishDate 2014
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-39799242014-04-11 Comprehensive Evaluation of Peripheral Nerve Regeneration in the Acute Healing Phase Using Tissue Clearing and Optical Microscopy in a Rodent Model Jung, Yookyung Ng, Joanna H. Keating, Cameron P. Senthil-Kumar, Prabhu Zhao, Jie Randolph, Mark A. Winograd, Jonathan M. Evans, Conor L. PLoS One Research Article Peripheral nerve injury (PNI), a common injury in both the civilian and military arenas, is usually associated with high healthcare costs and with patients enduring slow recovery times, diminished quality of life, and potential long-term disability. Patients with PNI typically undergo complex interventions but the factors that govern optimal response are not fully characterized. A fundamental understanding of the cellular and tissue-level events in the immediate postoperative period is essential for improving treatment and optimizing repair. Here, we demonstrate a comprehensive imaging approach to evaluate peripheral nerve axonal regeneration in a rodent PNI model using a tissue clearing method to improve depth penetration while preserving neural architecture. Sciatic nerve transaction and end-to-end repair were performed in both wild type and thy-1 GFP rats. The nerves were harvested at time points after repair before undergoing whole mount immunofluorescence staining and tissue clearing. By increasing the optic depth penetration, tissue clearing allowed the visualization and evaluation of Wallerian degeneration and nerve regrowth throughout entire sciatic nerves with subcellular resolution. The tissue clearing protocol did not affect immunofluorescence labeling and no observable decrease in the fluorescence signal was observed. Large-area, high-resolution tissue volumes could be quantified to provide structural and connectivity information not available from current gold-standard approaches for evaluating axonal regeneration following PNI. The results are suggestive of observed behavioral recovery in vivo after neurorrhaphy, providing a method of evaluating axonal regeneration following repair that can serve as an adjunct to current standard outcomes measurements. This study demonstrates that tissue clearing following whole mount immunofluorescence staining enables the complete visualization and quantitative evaluation of axons throughout nerves in a PNI model. The methods developed in this study could advance PNI research allowing both researchers and clinicians to further understand the individual events of axonal degeneration and regeneration on a multifaceted level. Public Library of Science 2014-04-08 /pmc/articles/PMC3979924/ /pubmed/24714405 http://dx.doi.org/10.1371/journal.pone.0094054 Text en © 2014 Jung 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
Jung, Yookyung
Ng, Joanna H.
Keating, Cameron P.
Senthil-Kumar, Prabhu
Zhao, Jie
Randolph, Mark A.
Winograd, Jonathan M.
Evans, Conor L.
Comprehensive Evaluation of Peripheral Nerve Regeneration in the Acute Healing Phase Using Tissue Clearing and Optical Microscopy in a Rodent Model
title Comprehensive Evaluation of Peripheral Nerve Regeneration in the Acute Healing Phase Using Tissue Clearing and Optical Microscopy in a Rodent Model
title_full Comprehensive Evaluation of Peripheral Nerve Regeneration in the Acute Healing Phase Using Tissue Clearing and Optical Microscopy in a Rodent Model
title_fullStr Comprehensive Evaluation of Peripheral Nerve Regeneration in the Acute Healing Phase Using Tissue Clearing and Optical Microscopy in a Rodent Model
title_full_unstemmed Comprehensive Evaluation of Peripheral Nerve Regeneration in the Acute Healing Phase Using Tissue Clearing and Optical Microscopy in a Rodent Model
title_short Comprehensive Evaluation of Peripheral Nerve Regeneration in the Acute Healing Phase Using Tissue Clearing and Optical Microscopy in a Rodent Model
title_sort comprehensive evaluation of peripheral nerve regeneration in the acute healing phase using tissue clearing and optical microscopy in a rodent model
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3979924/
https://www.ncbi.nlm.nih.gov/pubmed/24714405
http://dx.doi.org/10.1371/journal.pone.0094054
work_keys_str_mv AT jungyookyung comprehensiveevaluationofperipheralnerveregenerationintheacutehealingphaseusingtissueclearingandopticalmicroscopyinarodentmodel
AT ngjoannah comprehensiveevaluationofperipheralnerveregenerationintheacutehealingphaseusingtissueclearingandopticalmicroscopyinarodentmodel
AT keatingcameronp comprehensiveevaluationofperipheralnerveregenerationintheacutehealingphaseusingtissueclearingandopticalmicroscopyinarodentmodel
AT senthilkumarprabhu comprehensiveevaluationofperipheralnerveregenerationintheacutehealingphaseusingtissueclearingandopticalmicroscopyinarodentmodel
AT zhaojie comprehensiveevaluationofperipheralnerveregenerationintheacutehealingphaseusingtissueclearingandopticalmicroscopyinarodentmodel
AT randolphmarka comprehensiveevaluationofperipheralnerveregenerationintheacutehealingphaseusingtissueclearingandopticalmicroscopyinarodentmodel
AT winogradjonathanm comprehensiveevaluationofperipheralnerveregenerationintheacutehealingphaseusingtissueclearingandopticalmicroscopyinarodentmodel
AT evansconorl comprehensiveevaluationofperipheralnerveregenerationintheacutehealingphaseusingtissueclearingandopticalmicroscopyinarodentmodel