Cargando…
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...
Autores principales: | , , , , , |
---|---|
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 |
_version_ | 1782504769358659584 |
---|---|
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. |
format | Online Article Text |
id | pubmed-5291392 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT jiangyanfen visualizingtheentericnervoussystemusinggeneticallyengineereddoublereportermicecomparisonwithimmunofluorescence AT donghui visualizingtheentericnervoussystemusinggeneticallyengineereddoublereportermicecomparisonwithimmunofluorescence AT eckmannlars visualizingtheentericnervoussystemusinggeneticallyengineereddoublereportermicecomparisonwithimmunofluorescence AT hansonelainem visualizingtheentericnervoussystemusinggeneticallyengineereddoublereportermicecomparisonwithimmunofluorescence AT ihnkatherinec visualizingtheentericnervoussystemusinggeneticallyengineereddoublereportermicecomparisonwithimmunofluorescence AT mittalravinderk visualizingtheentericnervoussystemusinggeneticallyengineereddoublereportermicecomparisonwithimmunofluorescence |