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PrismPlus: a mouse line expressing distinct fluorophores in four different brain cell types

To screen the complex central nervous system (CNS) injury responses, we created a quadruple-labelled ‘PrismPlus’ mouse line with a genetically encoded distinct fluorescent tag in oligodendrocytes, microglia, neurons, and astrocytes. Cx3cr1-gfp and Prism mice originally developed by Jung et al., 2000...

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Autores principales: Gaire, Janak, Lee, Heui Chang, Ward, Ray, Currlin, Seth, Woolley, Andrew J., Coleman, Jason E., Williams, Justin C., Otto, Kevin J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5940666/
https://www.ncbi.nlm.nih.gov/pubmed/29739975
http://dx.doi.org/10.1038/s41598-018-25208-y
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author Gaire, Janak
Lee, Heui Chang
Ward, Ray
Currlin, Seth
Woolley, Andrew J.
Coleman, Jason E.
Williams, Justin C.
Otto, Kevin J.
author_facet Gaire, Janak
Lee, Heui Chang
Ward, Ray
Currlin, Seth
Woolley, Andrew J.
Coleman, Jason E.
Williams, Justin C.
Otto, Kevin J.
author_sort Gaire, Janak
collection PubMed
description To screen the complex central nervous system (CNS) injury responses, we created a quadruple-labelled ‘PrismPlus’ mouse line with a genetically encoded distinct fluorescent tag in oligodendrocytes, microglia, neurons, and astrocytes. Cx3cr1-gfp and Prism mice originally developed by Jung et al., 2000 and Dougherty et al., 2012, respectively, were cross-bred. First, we confirmed the presence of fluorophores in appropriate cell types in PrismPlus mice. PrismPlus mice were then used to examine the cellular responses to brain implanted micro-devices. We observed an increase in microglial response at earlier time points as compared to 4 weeks, a progressive astrocytic response, and fewer neurons at the vicinity of an implanted device. These results are similar to what has been described in literature using other rodent strains, previously attainable only through time-consuming and variable immunohistochemistry methods. Finally, we demonstrate the compatibility of PrismPlus brain tissue with CLARITY, an advanced tissue clearing technique, opening the door to future thick tissue imaging studies. This report confirms PrismPlus transgenic fluorescence and highlights the utility of these mice to study CNS injuries. The work herein seeks to establish a novel transgenic mouse line to improve experimental scope, consistency, and efficiency for CNS researchers.
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spelling pubmed-59406662018-05-11 PrismPlus: a mouse line expressing distinct fluorophores in four different brain cell types Gaire, Janak Lee, Heui Chang Ward, Ray Currlin, Seth Woolley, Andrew J. Coleman, Jason E. Williams, Justin C. Otto, Kevin J. Sci Rep Article To screen the complex central nervous system (CNS) injury responses, we created a quadruple-labelled ‘PrismPlus’ mouse line with a genetically encoded distinct fluorescent tag in oligodendrocytes, microglia, neurons, and astrocytes. Cx3cr1-gfp and Prism mice originally developed by Jung et al., 2000 and Dougherty et al., 2012, respectively, were cross-bred. First, we confirmed the presence of fluorophores in appropriate cell types in PrismPlus mice. PrismPlus mice were then used to examine the cellular responses to brain implanted micro-devices. We observed an increase in microglial response at earlier time points as compared to 4 weeks, a progressive astrocytic response, and fewer neurons at the vicinity of an implanted device. These results are similar to what has been described in literature using other rodent strains, previously attainable only through time-consuming and variable immunohistochemistry methods. Finally, we demonstrate the compatibility of PrismPlus brain tissue with CLARITY, an advanced tissue clearing technique, opening the door to future thick tissue imaging studies. This report confirms PrismPlus transgenic fluorescence and highlights the utility of these mice to study CNS injuries. The work herein seeks to establish a novel transgenic mouse line to improve experimental scope, consistency, and efficiency for CNS researchers. Nature Publishing Group UK 2018-05-08 /pmc/articles/PMC5940666/ /pubmed/29739975 http://dx.doi.org/10.1038/s41598-018-25208-y Text en © The Author(s) 2018 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/.
spellingShingle Article
Gaire, Janak
Lee, Heui Chang
Ward, Ray
Currlin, Seth
Woolley, Andrew J.
Coleman, Jason E.
Williams, Justin C.
Otto, Kevin J.
PrismPlus: a mouse line expressing distinct fluorophores in four different brain cell types
title PrismPlus: a mouse line expressing distinct fluorophores in four different brain cell types
title_full PrismPlus: a mouse line expressing distinct fluorophores in four different brain cell types
title_fullStr PrismPlus: a mouse line expressing distinct fluorophores in four different brain cell types
title_full_unstemmed PrismPlus: a mouse line expressing distinct fluorophores in four different brain cell types
title_short PrismPlus: a mouse line expressing distinct fluorophores in four different brain cell types
title_sort prismplus: a mouse line expressing distinct fluorophores in four different brain cell types
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5940666/
https://www.ncbi.nlm.nih.gov/pubmed/29739975
http://dx.doi.org/10.1038/s41598-018-25208-y
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