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Visualizing the enteric nervous system using genetically engineered double reporter mice: Comparison with immunofluorescence

BACKGROUND AND AIMS: The enteric nervous system (ENS) plays a crucial role in the control of gastrointestinal motility, secretion and absorption functions. Immunohistochemistry has been widely used to visualize neurons of the ENS for more than two decades. Genetically engineered mice that report spe...

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Autores principales: Jiang, Yanfen, Dong, Hui, Eckmann, Lars, Hanson, Elaine M., Ihn, Katherine C., Mittal, Ravinder K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5291392/
https://www.ncbi.nlm.nih.gov/pubmed/28158225
http://dx.doi.org/10.1371/journal.pone.0171239
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author Jiang, Yanfen
Dong, Hui
Eckmann, Lars
Hanson, Elaine M.
Ihn, Katherine C.
Mittal, Ravinder K.
author_facet Jiang, Yanfen
Dong, Hui
Eckmann, Lars
Hanson, Elaine M.
Ihn, Katherine C.
Mittal, Ravinder K.
author_sort Jiang, Yanfen
collection PubMed
description BACKGROUND AND AIMS: The enteric nervous system (ENS) plays a crucial role in the control of gastrointestinal motility, secretion and absorption functions. Immunohistochemistry has been widely used to visualize neurons of the ENS for more than two decades. Genetically engineered mice that report specific proteins can also be used to visualize neurons of the ENS. The goal of our study was to develop a mouse that expresses fluorescent neuronal nitric oxide synthase (nNOS) and choline acetyltransferase (ChAT), the two proteins expressed in 95% of the ENS neurons. We compared ENS neurons visualized in the reporter mouse with the wild type mouse stained using classical immunostaining techniques. METHODS: Mice hemizygous for ChAT-ChR2-YFP BAC transgene with expression of the mhChR2:YFP fusion protein directed by ChAT promoter/enhancer regions on the BAC transgene were purchased commercially. The Cre/LoxP technique of somatic recombination was used to construct mice with nNOS positive neurons. The two mice were crossbred and tissues were harvested and examined using fluorescent microscopy. Immunostaining was performed in the wild type mice, using antibodies to nNOS, ChAT, Hu and PGP 9.5. RESULTS: Greater than 95% of the ENS neurons were positive for either nNOS or ChAT or both. The nNOS and ChAT neurons and their processes in the ENS were well visualized in all the regions of the GI tract, i.e., esophagus, small intestine and colon. The number of nNOS and ChAT neurons was approximately same in the reporter mouse and immunostaining method in the wild type mouse. The nNOS fluorescence in the reporter mouse was seen in both cytoplasm as well as nucleus but in the immunostained specimens it was seen only in the cytoplasm. CONCLUSION: We propose that the genetically engineered double reporter mouse for ChAT and nNOS proteins is a powerful tool to study of the effects of various diseases on the ENS without the need for immunostaining.
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spelling pubmed-52913922017-02-17 Visualizing the enteric nervous system using genetically engineered double reporter mice: Comparison with immunofluorescence Jiang, Yanfen Dong, Hui Eckmann, Lars Hanson, Elaine M. Ihn, Katherine C. Mittal, Ravinder K. PLoS One Research Article BACKGROUND AND AIMS: The enteric nervous system (ENS) plays a crucial role in the control of gastrointestinal motility, secretion and absorption functions. Immunohistochemistry has been widely used to visualize neurons of the ENS for more than two decades. Genetically engineered mice that report specific proteins can also be used to visualize neurons of the ENS. The goal of our study was to develop a mouse that expresses fluorescent neuronal nitric oxide synthase (nNOS) and choline acetyltransferase (ChAT), the two proteins expressed in 95% of the ENS neurons. We compared ENS neurons visualized in the reporter mouse with the wild type mouse stained using classical immunostaining techniques. METHODS: Mice hemizygous for ChAT-ChR2-YFP BAC transgene with expression of the mhChR2:YFP fusion protein directed by ChAT promoter/enhancer regions on the BAC transgene were purchased commercially. The Cre/LoxP technique of somatic recombination was used to construct mice with nNOS positive neurons. The two mice were crossbred and tissues were harvested and examined using fluorescent microscopy. Immunostaining was performed in the wild type mice, using antibodies to nNOS, ChAT, Hu and PGP 9.5. RESULTS: Greater than 95% of the ENS neurons were positive for either nNOS or ChAT or both. The nNOS and ChAT neurons and their processes in the ENS were well visualized in all the regions of the GI tract, i.e., esophagus, small intestine and colon. The number of nNOS and ChAT neurons was approximately same in the reporter mouse and immunostaining method in the wild type mouse. The nNOS fluorescence in the reporter mouse was seen in both cytoplasm as well as nucleus but in the immunostained specimens it was seen only in the cytoplasm. CONCLUSION: We propose that the genetically engineered double reporter mouse for ChAT and nNOS proteins is a powerful tool to study of the effects of various diseases on the ENS without the need for immunostaining. Public Library of Science 2017-02-03 /pmc/articles/PMC5291392/ /pubmed/28158225 http://dx.doi.org/10.1371/journal.pone.0171239 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Jiang, Yanfen
Dong, Hui
Eckmann, Lars
Hanson, Elaine M.
Ihn, Katherine C.
Mittal, Ravinder K.
Visualizing the enteric nervous system using genetically engineered double reporter mice: Comparison with immunofluorescence
title Visualizing the enteric nervous system using genetically engineered double reporter mice: Comparison with immunofluorescence
title_full Visualizing the enteric nervous system using genetically engineered double reporter mice: Comparison with immunofluorescence
title_fullStr Visualizing the enteric nervous system using genetically engineered double reporter mice: Comparison with immunofluorescence
title_full_unstemmed Visualizing the enteric nervous system using genetically engineered double reporter mice: Comparison with immunofluorescence
title_short Visualizing the enteric nervous system using genetically engineered double reporter mice: Comparison with immunofluorescence
title_sort visualizing the enteric nervous system using genetically engineered double reporter mice: comparison with immunofluorescence
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5291392/
https://www.ncbi.nlm.nih.gov/pubmed/28158225
http://dx.doi.org/10.1371/journal.pone.0171239
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