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Alpha2 Macroglobulin-Like Is Essential for Liver Development in Zebrafish

BACKGROUND: Alpha 2 Macroglobulin family members have been studied extensively with respect to their roles in physiology and human disease including innate immunity and Alzheimer's disease, but little is known about a possible role in liver development loss-of-function in model systems. PRINCIP...

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Detalles Bibliográficos
Autores principales: Hong, Sung-Kook, Dawid, Igor B.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2581608/
https://www.ncbi.nlm.nih.gov/pubmed/19011686
http://dx.doi.org/10.1371/journal.pone.0003736
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author Hong, Sung-Kook
Dawid, Igor B.
author_facet Hong, Sung-Kook
Dawid, Igor B.
author_sort Hong, Sung-Kook
collection PubMed
description BACKGROUND: Alpha 2 Macroglobulin family members have been studied extensively with respect to their roles in physiology and human disease including innate immunity and Alzheimer's disease, but little is known about a possible role in liver development loss-of-function in model systems. PRINCIPAL FINDINGS: We report the isolation of the zebrafish α2 macroglobulin-like (A2ML) gene and its specific expression in the liver during differentiation. Morpholino-based knock-down of A2ML did not block the initial formation of the liver primordium, but inhibited liver growth and differentiation. SIGNIFICANCE: This report on A2ML function in zebrafish development provides the first evidence for a specific role of an A2M family gene in liver formation during early embryogenesis in a vertebrate.
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spelling pubmed-25816082008-11-17 Alpha2 Macroglobulin-Like Is Essential for Liver Development in Zebrafish Hong, Sung-Kook Dawid, Igor B. PLoS One Research Article BACKGROUND: Alpha 2 Macroglobulin family members have been studied extensively with respect to their roles in physiology and human disease including innate immunity and Alzheimer's disease, but little is known about a possible role in liver development loss-of-function in model systems. PRINCIPAL FINDINGS: We report the isolation of the zebrafish α2 macroglobulin-like (A2ML) gene and its specific expression in the liver during differentiation. Morpholino-based knock-down of A2ML did not block the initial formation of the liver primordium, but inhibited liver growth and differentiation. SIGNIFICANCE: This report on A2ML function in zebrafish development provides the first evidence for a specific role of an A2M family gene in liver formation during early embryogenesis in a vertebrate. Public Library of Science 2008-11-17 /pmc/articles/PMC2581608/ /pubmed/19011686 http://dx.doi.org/10.1371/journal.pone.0003736 Text en This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Hong, Sung-Kook
Dawid, Igor B.
Alpha2 Macroglobulin-Like Is Essential for Liver Development in Zebrafish
title Alpha2 Macroglobulin-Like Is Essential for Liver Development in Zebrafish
title_full Alpha2 Macroglobulin-Like Is Essential for Liver Development in Zebrafish
title_fullStr Alpha2 Macroglobulin-Like Is Essential for Liver Development in Zebrafish
title_full_unstemmed Alpha2 Macroglobulin-Like Is Essential for Liver Development in Zebrafish
title_short Alpha2 Macroglobulin-Like Is Essential for Liver Development in Zebrafish
title_sort alpha2 macroglobulin-like is essential for liver development in zebrafish
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2581608/
https://www.ncbi.nlm.nih.gov/pubmed/19011686
http://dx.doi.org/10.1371/journal.pone.0003736
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