Zebrafish as a model to study live mucus physiology

Dysfunctional mucus barriers can result in important pulmonary and gastrointestinal conditions, but model systems to study the underlying causes are largely missing. We identified and characterized five mucin homologues in zebrafish, and demonstrated a strategy for fluorescence labeling of one selec...

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Main Authors: Jevtov, Irena, Samuelsson, Tore, Yao, Grace, Amsterdam, Adam, Ribbeck, Katharina
Other Authors: Massachusetts Institute of Technology. Department of Biological Engineering
Format: Article
Language:en_US
Published: Nature Publishing Group 2014
Online Access:http://hdl.handle.net/1721.1/92571
https://orcid.org/0000-0001-8260-338X
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author Jevtov, Irena
Samuelsson, Tore
Yao, Grace
Amsterdam, Adam
Ribbeck, Katharina
author2 Massachusetts Institute of Technology. Department of Biological Engineering
author_facet Massachusetts Institute of Technology. Department of Biological Engineering
Jevtov, Irena
Samuelsson, Tore
Yao, Grace
Amsterdam, Adam
Ribbeck, Katharina
author_sort Jevtov, Irena
collection MIT
description Dysfunctional mucus barriers can result in important pulmonary and gastrointestinal conditions, but model systems to study the underlying causes are largely missing. We identified and characterized five mucin homologues in zebrafish, and demonstrated a strategy for fluorescence labeling of one selected mucin. These tools can be used for in vivo experiments and in pharmacological and genetic screens to study the dynamics and mechanisms of mucosal physiology.
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spelling mit-1721.1/925712022-10-01T09:55:01Z Zebrafish as a model to study live mucus physiology Jevtov, Irena Samuelsson, Tore Yao, Grace Amsterdam, Adam Ribbeck, Katharina Massachusetts Institute of Technology. Department of Biological Engineering Koch Institute for Integrative Cancer Research at MIT Amsterdam, Adam Ribbeck, Katharina Jevtov, Irena Yao, Grace Dysfunctional mucus barriers can result in important pulmonary and gastrointestinal conditions, but model systems to study the underlying causes are largely missing. We identified and characterized five mucin homologues in zebrafish, and demonstrated a strategy for fluorescence labeling of one selected mucin. These tools can be used for in vivo experiments and in pharmacological and genetic screens to study the dynamics and mechanisms of mucosal physiology. National Institute of Environmental Health Sciences (Grant P30-ES002109) Johnson & Johnson. Corporate Office of Science and Technology National Institutes of Health (U.S.) (Grant CA106416) Kathy and Curt Marble Cancer Research Fund David H. Koch Institute for Integrative Cancer Research at MIT (Zebrafish Core Facility) 2014-12-31T20:06:59Z 2014-12-31T20:06:59Z 2014-10 2014-04 Article http://purl.org/eprint/type/JournalArticle 2045-2322 http://hdl.handle.net/1721.1/92571 Jevtov, Irena, Tore Samuelsson, Grace Yao, Adam Amsterdam, and Katharina Ribbeck. “Zebrafish as a Model to Study Live Mucus Physiology.” Sci. Rep. 4 (October 17, 2014): 6653. https://orcid.org/0000-0001-8260-338X en_US http://dx.doi.org/10.1038/srep06653 Scientific Reports Creative Commons Attribution http://creativecommons.org/licenses/by-nc-nd/4.0/ application/pdf Nature Publishing Group Nature Publishing Group
spellingShingle Jevtov, Irena
Samuelsson, Tore
Yao, Grace
Amsterdam, Adam
Ribbeck, Katharina
Zebrafish as a model to study live mucus physiology
title Zebrafish as a model to study live mucus physiology
title_full Zebrafish as a model to study live mucus physiology
title_fullStr Zebrafish as a model to study live mucus physiology
title_full_unstemmed Zebrafish as a model to study live mucus physiology
title_short Zebrafish as a model to study live mucus physiology
title_sort zebrafish as a model to study live mucus physiology
url http://hdl.handle.net/1721.1/92571
https://orcid.org/0000-0001-8260-338X
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