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A Novel In Vivo Model for Multiplexed Analysis of Callosal Connections upon Cortical Damage
Brain damage is the major cause of permanent disability and it is particularly relevant in the elderly. While most studies focused on the immediate phase of neuronal loss upon injury, much less is known about the process of axonal regeneration after damage. The development of new refined preclinical...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9368090/ https://www.ncbi.nlm.nih.gov/pubmed/35897791 http://dx.doi.org/10.3390/ijms23158224 |
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author | González-Manteiga, Ana Navarro-González, Carmen Sebestyén, Valentina Evita Saborit-Torres, Jose Manuel Talhada, Daniela Vayá, María de la Iglesia Ruscher, Karsten Fazzari, Pietro |
author_facet | González-Manteiga, Ana Navarro-González, Carmen Sebestyén, Valentina Evita Saborit-Torres, Jose Manuel Talhada, Daniela Vayá, María de la Iglesia Ruscher, Karsten Fazzari, Pietro |
author_sort | González-Manteiga, Ana |
collection | PubMed |
description | Brain damage is the major cause of permanent disability and it is particularly relevant in the elderly. While most studies focused on the immediate phase of neuronal loss upon injury, much less is known about the process of axonal regeneration after damage. The development of new refined preclinical models to investigate neuronal regeneration and the recovery of brain tissue upon injury is a major unmet challenge. Here, we present a novel experimental paradigm in mice that entails the (i) tracing of cortico-callosal connections, (ii) a mechanical lesion of the motor cortex, (iii) the stereological and histological analysis of the damaged tissue, and (iv) the functional characterization of motor deficits. By combining conventional microscopy with semi-automated 3D reconstruction, this approach allows the analysis of fine subcellular structures, such as axonal terminals, with the tridimensional overview of the connectivity and tissue integrity around the lesioned area. Since this 3D reconstruction is performed in serial sections, multiple labeling can be performed by combining diverse histological markers. We provide an example of how this methodology can be used to study cellular interactions. Namely, we show the correlation between active microglial cells and the perineuronal nets that envelop parvalbumin interneurons. In conclusion, this novel experimental paradigm will contribute to a better understanding of the molecular and cellular interactions underpinning the process of cortical regeneration upon brain damage. |
format | Online Article Text |
id | pubmed-9368090 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-93680902022-08-12 A Novel In Vivo Model for Multiplexed Analysis of Callosal Connections upon Cortical Damage González-Manteiga, Ana Navarro-González, Carmen Sebestyén, Valentina Evita Saborit-Torres, Jose Manuel Talhada, Daniela Vayá, María de la Iglesia Ruscher, Karsten Fazzari, Pietro Int J Mol Sci Article Brain damage is the major cause of permanent disability and it is particularly relevant in the elderly. While most studies focused on the immediate phase of neuronal loss upon injury, much less is known about the process of axonal regeneration after damage. The development of new refined preclinical models to investigate neuronal regeneration and the recovery of brain tissue upon injury is a major unmet challenge. Here, we present a novel experimental paradigm in mice that entails the (i) tracing of cortico-callosal connections, (ii) a mechanical lesion of the motor cortex, (iii) the stereological and histological analysis of the damaged tissue, and (iv) the functional characterization of motor deficits. By combining conventional microscopy with semi-automated 3D reconstruction, this approach allows the analysis of fine subcellular structures, such as axonal terminals, with the tridimensional overview of the connectivity and tissue integrity around the lesioned area. Since this 3D reconstruction is performed in serial sections, multiple labeling can be performed by combining diverse histological markers. We provide an example of how this methodology can be used to study cellular interactions. Namely, we show the correlation between active microglial cells and the perineuronal nets that envelop parvalbumin interneurons. In conclusion, this novel experimental paradigm will contribute to a better understanding of the molecular and cellular interactions underpinning the process of cortical regeneration upon brain damage. MDPI 2022-07-26 /pmc/articles/PMC9368090/ /pubmed/35897791 http://dx.doi.org/10.3390/ijms23158224 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article González-Manteiga, Ana Navarro-González, Carmen Sebestyén, Valentina Evita Saborit-Torres, Jose Manuel Talhada, Daniela Vayá, María de la Iglesia Ruscher, Karsten Fazzari, Pietro A Novel In Vivo Model for Multiplexed Analysis of Callosal Connections upon Cortical Damage |
title | A Novel In Vivo Model for Multiplexed Analysis of Callosal Connections upon Cortical Damage |
title_full | A Novel In Vivo Model for Multiplexed Analysis of Callosal Connections upon Cortical Damage |
title_fullStr | A Novel In Vivo Model for Multiplexed Analysis of Callosal Connections upon Cortical Damage |
title_full_unstemmed | A Novel In Vivo Model for Multiplexed Analysis of Callosal Connections upon Cortical Damage |
title_short | A Novel In Vivo Model for Multiplexed Analysis of Callosal Connections upon Cortical Damage |
title_sort | novel in vivo model for multiplexed analysis of callosal connections upon cortical damage |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9368090/ https://www.ncbi.nlm.nih.gov/pubmed/35897791 http://dx.doi.org/10.3390/ijms23158224 |
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