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Near infrared readouts offer sensitive and rapid assessments of intestinal permeability and disease severity in inflammatory bowel disease models
Intestinal permeability and neutrophil activity are closely linked to inflammatory bowel disease (IBD) pathophysiology. Here we discuss two techniques for assessing permeability and neutrophil activity in mouse IBD models using near infrared (NIR) detection. To address the limitation of visible ligh...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7070059/ https://www.ncbi.nlm.nih.gov/pubmed/32170183 http://dx.doi.org/10.1038/s41598-020-61756-y |
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author | Zhang, Liang Wallace, Craig D. Erickson, Jamie E. Nelson, Christine M. Gaudette, Stephanie M. Pohl, Calvin S. Karsen, Samuel D. Simler, Gricelda H. Peng, Ruoqi Stedman, Christopher A. Laroux, F. Stephen Wurbel, Marc A. Kamath, Rajesh V. McRae, Bradford L. Schwartz Sterman, Annette J. Mitra, Soumya |
author_facet | Zhang, Liang Wallace, Craig D. Erickson, Jamie E. Nelson, Christine M. Gaudette, Stephanie M. Pohl, Calvin S. Karsen, Samuel D. Simler, Gricelda H. Peng, Ruoqi Stedman, Christopher A. Laroux, F. Stephen Wurbel, Marc A. Kamath, Rajesh V. McRae, Bradford L. Schwartz Sterman, Annette J. Mitra, Soumya |
author_sort | Zhang, Liang |
collection | PubMed |
description | Intestinal permeability and neutrophil activity are closely linked to inflammatory bowel disease (IBD) pathophysiology. Here we discuss two techniques for assessing permeability and neutrophil activity in mouse IBD models using near infrared (NIR) detection. To address the limitation of visible light readouts—namely high background—IRDye 800CW was used to enable rapid, non-terminal measurements of intestinal permeability. The increased sensitivity of NIR readouts for colon permeability is shown using dextran sulfate sodium (DSS) and anti-CD40 murine colitis models in response to interleukin-22 immunoglobulin Fc (IL22Fc) fusion protein and anti-p40 monoclonal antibody treatments, respectively. In addition to enhanced permeability, elevated levels of neutrophil elastase (NE) have been reported in inflamed colonic mucosal tissue. Activatable NIR fluorescent probes have been extensively used for disease activity evaluation in oncologic animal models, and we demonstrate their translatability using a NE-activatable reagent to evaluate inflammation in DSS mice. Confocal laser endomicroscopy (CLE) and tissue imaging allow visualization of spatial NE activity throughout diseased colon as well as changes in disease severity from IL22Fc treatment. Our findings with the 800CW dye and the NE probe highlight the ease of their implementation in preclinical IBD research. |
format | Online Article Text |
id | pubmed-7070059 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70700592020-03-22 Near infrared readouts offer sensitive and rapid assessments of intestinal permeability and disease severity in inflammatory bowel disease models Zhang, Liang Wallace, Craig D. Erickson, Jamie E. Nelson, Christine M. Gaudette, Stephanie M. Pohl, Calvin S. Karsen, Samuel D. Simler, Gricelda H. Peng, Ruoqi Stedman, Christopher A. Laroux, F. Stephen Wurbel, Marc A. Kamath, Rajesh V. McRae, Bradford L. Schwartz Sterman, Annette J. Mitra, Soumya Sci Rep Article Intestinal permeability and neutrophil activity are closely linked to inflammatory bowel disease (IBD) pathophysiology. Here we discuss two techniques for assessing permeability and neutrophil activity in mouse IBD models using near infrared (NIR) detection. To address the limitation of visible light readouts—namely high background—IRDye 800CW was used to enable rapid, non-terminal measurements of intestinal permeability. The increased sensitivity of NIR readouts for colon permeability is shown using dextran sulfate sodium (DSS) and anti-CD40 murine colitis models in response to interleukin-22 immunoglobulin Fc (IL22Fc) fusion protein and anti-p40 monoclonal antibody treatments, respectively. In addition to enhanced permeability, elevated levels of neutrophil elastase (NE) have been reported in inflamed colonic mucosal tissue. Activatable NIR fluorescent probes have been extensively used for disease activity evaluation in oncologic animal models, and we demonstrate their translatability using a NE-activatable reagent to evaluate inflammation in DSS mice. Confocal laser endomicroscopy (CLE) and tissue imaging allow visualization of spatial NE activity throughout diseased colon as well as changes in disease severity from IL22Fc treatment. Our findings with the 800CW dye and the NE probe highlight the ease of their implementation in preclinical IBD research. Nature Publishing Group UK 2020-03-13 /pmc/articles/PMC7070059/ /pubmed/32170183 http://dx.doi.org/10.1038/s41598-020-61756-y Text en © The Author(s) 2020 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 Zhang, Liang Wallace, Craig D. Erickson, Jamie E. Nelson, Christine M. Gaudette, Stephanie M. Pohl, Calvin S. Karsen, Samuel D. Simler, Gricelda H. Peng, Ruoqi Stedman, Christopher A. Laroux, F. Stephen Wurbel, Marc A. Kamath, Rajesh V. McRae, Bradford L. Schwartz Sterman, Annette J. Mitra, Soumya Near infrared readouts offer sensitive and rapid assessments of intestinal permeability and disease severity in inflammatory bowel disease models |
title | Near infrared readouts offer sensitive and rapid assessments of intestinal permeability and disease severity in inflammatory bowel disease models |
title_full | Near infrared readouts offer sensitive and rapid assessments of intestinal permeability and disease severity in inflammatory bowel disease models |
title_fullStr | Near infrared readouts offer sensitive and rapid assessments of intestinal permeability and disease severity in inflammatory bowel disease models |
title_full_unstemmed | Near infrared readouts offer sensitive and rapid assessments of intestinal permeability and disease severity in inflammatory bowel disease models |
title_short | Near infrared readouts offer sensitive and rapid assessments of intestinal permeability and disease severity in inflammatory bowel disease models |
title_sort | near infrared readouts offer sensitive and rapid assessments of intestinal permeability and disease severity in inflammatory bowel disease models |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7070059/ https://www.ncbi.nlm.nih.gov/pubmed/32170183 http://dx.doi.org/10.1038/s41598-020-61756-y |
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