A high-throughput chemically induced inflammation assay in zebrafish

<p>Abstract</p> <p>Background</p> <p>Studies on innate immunity have benefited from the introduction of zebrafish as a model system. Transgenic fish expressing fluorescent proteins in leukocyte populations allow direct, quantitative visualization of an inflammatory resp...

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Main Authors: Liebel Urban, Loosli Felix, Jones Rebecca A, Gallardo Viviana E, Wittmann Christine, Peña Oscar A, d'Alençon Claudia A, Grabher Clemens, Allende Miguel L
Format: Article
Language:English
Published: BMC 2010-12-01
Series:BMC Biology
Online Access:http://www.biomedcentral.com/1741-7007/8/151
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author Liebel Urban
Loosli Felix
Jones Rebecca A
Gallardo Viviana E
Wittmann Christine
Peña Oscar A
d'Alençon Claudia A
Grabher Clemens
Allende Miguel L
author_facet Liebel Urban
Loosli Felix
Jones Rebecca A
Gallardo Viviana E
Wittmann Christine
Peña Oscar A
d'Alençon Claudia A
Grabher Clemens
Allende Miguel L
author_sort Liebel Urban
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>Studies on innate immunity have benefited from the introduction of zebrafish as a model system. Transgenic fish expressing fluorescent proteins in leukocyte populations allow direct, quantitative visualization of an inflammatory response <it>in vivo</it>. It has been proposed that this animal model can be used for high-throughput screens aimed at the identification of novel immunomodulatory lead compounds. However, current assays require invasive manipulation of fish individually, thus preventing high-content screening.</p> <p>Results</p> <p>Here we show that specific, noninvasive damage to lateral line neuromast cells can induce a robust acute inflammatory response. Exposure of fish larvae to sublethal concentrations of copper sulfate selectively damages the sensory hair cell population inducing infiltration of leukocytes to neuromasts within 20 minutes. Inflammation can be assayed in real time using transgenic fish expressing fluorescent proteins in leukocytes or by histochemical assays in fixed larvae. We demonstrate the usefulness of this method for chemical and genetic screens to detect the effect of immunomodulatory compounds and mutations affecting the leukocyte response. Moreover, we transformed the assay into a high-throughput screening method by using a customized automated imaging and processing system that quantifies the magnitude of the inflammatory reaction.</p> <p>Conclusions</p> <p>This approach allows rapid screening of thousands of compounds or mutagenized zebrafish for effects on inflammation and enables the identification of novel players in the regulation of innate immunity and potential lead compounds toward new immunomodulatory therapies. We have called this method the chemically induced inflammation assay, or ChIn assay.</p> <p>See Commentary article: <url>http://www.biomedcentral.com/1741-7007/8/148</url>.</p>
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spelling doaj.art-641e9527da8d482fab27e026facefc192022-12-21T22:50:50ZengBMCBMC Biology1741-70072010-12-018115110.1186/1741-7007-8-151A high-throughput chemically induced inflammation assay in zebrafishLiebel UrbanLoosli FelixJones Rebecca AGallardo Viviana EWittmann ChristinePeña Oscar Ad'Alençon Claudia AGrabher ClemensAllende Miguel L<p>Abstract</p> <p>Background</p> <p>Studies on innate immunity have benefited from the introduction of zebrafish as a model system. Transgenic fish expressing fluorescent proteins in leukocyte populations allow direct, quantitative visualization of an inflammatory response <it>in vivo</it>. It has been proposed that this animal model can be used for high-throughput screens aimed at the identification of novel immunomodulatory lead compounds. However, current assays require invasive manipulation of fish individually, thus preventing high-content screening.</p> <p>Results</p> <p>Here we show that specific, noninvasive damage to lateral line neuromast cells can induce a robust acute inflammatory response. Exposure of fish larvae to sublethal concentrations of copper sulfate selectively damages the sensory hair cell population inducing infiltration of leukocytes to neuromasts within 20 minutes. Inflammation can be assayed in real time using transgenic fish expressing fluorescent proteins in leukocytes or by histochemical assays in fixed larvae. We demonstrate the usefulness of this method for chemical and genetic screens to detect the effect of immunomodulatory compounds and mutations affecting the leukocyte response. Moreover, we transformed the assay into a high-throughput screening method by using a customized automated imaging and processing system that quantifies the magnitude of the inflammatory reaction.</p> <p>Conclusions</p> <p>This approach allows rapid screening of thousands of compounds or mutagenized zebrafish for effects on inflammation and enables the identification of novel players in the regulation of innate immunity and potential lead compounds toward new immunomodulatory therapies. We have called this method the chemically induced inflammation assay, or ChIn assay.</p> <p>See Commentary article: <url>http://www.biomedcentral.com/1741-7007/8/148</url>.</p>http://www.biomedcentral.com/1741-7007/8/151
spellingShingle Liebel Urban
Loosli Felix
Jones Rebecca A
Gallardo Viviana E
Wittmann Christine
Peña Oscar A
d'Alençon Claudia A
Grabher Clemens
Allende Miguel L
A high-throughput chemically induced inflammation assay in zebrafish
BMC Biology
title A high-throughput chemically induced inflammation assay in zebrafish
title_full A high-throughput chemically induced inflammation assay in zebrafish
title_fullStr A high-throughput chemically induced inflammation assay in zebrafish
title_full_unstemmed A high-throughput chemically induced inflammation assay in zebrafish
title_short A high-throughput chemically induced inflammation assay in zebrafish
title_sort high throughput chemically induced inflammation assay in zebrafish
url http://www.biomedcentral.com/1741-7007/8/151
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