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ABCC6 deficiency is associated with activation of BMP signaling in liver and kidney

Mutations in ABCC6 (ATP-binding cassette, subfamily C, member 6), an orphan transporter expressed in the liver, are the cause of pseudoxanthoma elasticum. Since ABCC6 was reported to affect matrix Gla protein (MGP), an inhibitor of bone morphogenetic proteins (BMPs), we studied BMP signaling and exp...

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Detalles Bibliográficos
Autores principales: Blazquez-Medela, Ana M., Guihard, Pierre J., Yao, Jiayi, Jumabay, Medet, Lusis, Aldons J., Boström, Kristina I., Yao, Yucheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4398664/
https://www.ncbi.nlm.nih.gov/pubmed/25893161
http://dx.doi.org/10.1016/j.fob.2015.03.009
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author Blazquez-Medela, Ana M.
Guihard, Pierre J.
Yao, Jiayi
Jumabay, Medet
Lusis, Aldons J.
Boström, Kristina I.
Yao, Yucheng
author_facet Blazquez-Medela, Ana M.
Guihard, Pierre J.
Yao, Jiayi
Jumabay, Medet
Lusis, Aldons J.
Boström, Kristina I.
Yao, Yucheng
author_sort Blazquez-Medela, Ana M.
collection PubMed
description Mutations in ABCC6 (ATP-binding cassette, subfamily C, member 6), an orphan transporter expressed in the liver, are the cause of pseudoxanthoma elasticum. Since ABCC6 was reported to affect matrix Gla protein (MGP), an inhibitor of bone morphogenetic proteins (BMPs), we studied BMP signaling and expression in various tissues of mice with and without functional ABCC. Enhanced BMP signaling was found in all examined tissues in the absence of ABCC6. Despite this, the expression of particular BMP proteins varied widely between tissues. Interestingly, the expression of most BMP proteins in the liver moved in the opposite direction to the same BMP proteins in kidneys in response to ABCC6 alterations. Thus, ABCC6 deficiency stimulates BMP signaling by acting on the expression of multiple BMPs.
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spelling pubmed-43986642015-04-17 ABCC6 deficiency is associated with activation of BMP signaling in liver and kidney Blazquez-Medela, Ana M. Guihard, Pierre J. Yao, Jiayi Jumabay, Medet Lusis, Aldons J. Boström, Kristina I. Yao, Yucheng FEBS Open Bio Article Mutations in ABCC6 (ATP-binding cassette, subfamily C, member 6), an orphan transporter expressed in the liver, are the cause of pseudoxanthoma elasticum. Since ABCC6 was reported to affect matrix Gla protein (MGP), an inhibitor of bone morphogenetic proteins (BMPs), we studied BMP signaling and expression in various tissues of mice with and without functional ABCC. Enhanced BMP signaling was found in all examined tissues in the absence of ABCC6. Despite this, the expression of particular BMP proteins varied widely between tissues. Interestingly, the expression of most BMP proteins in the liver moved in the opposite direction to the same BMP proteins in kidneys in response to ABCC6 alterations. Thus, ABCC6 deficiency stimulates BMP signaling by acting on the expression of multiple BMPs. Elsevier 2015-03-23 /pmc/articles/PMC4398664/ /pubmed/25893161 http://dx.doi.org/10.1016/j.fob.2015.03.009 Text en © 2015 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Blazquez-Medela, Ana M.
Guihard, Pierre J.
Yao, Jiayi
Jumabay, Medet
Lusis, Aldons J.
Boström, Kristina I.
Yao, Yucheng
ABCC6 deficiency is associated with activation of BMP signaling in liver and kidney
title ABCC6 deficiency is associated with activation of BMP signaling in liver and kidney
title_full ABCC6 deficiency is associated with activation of BMP signaling in liver and kidney
title_fullStr ABCC6 deficiency is associated with activation of BMP signaling in liver and kidney
title_full_unstemmed ABCC6 deficiency is associated with activation of BMP signaling in liver and kidney
title_short ABCC6 deficiency is associated with activation of BMP signaling in liver and kidney
title_sort abcc6 deficiency is associated with activation of bmp signaling in liver and kidney
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4398664/
https://www.ncbi.nlm.nih.gov/pubmed/25893161
http://dx.doi.org/10.1016/j.fob.2015.03.009
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