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Metformin Inhibits Cyst Formation in a Zebrafish Model of Polycystin-2 Deficiency
Autosomal dominant polycystic kidney disease (ADPKD) is a common kidney disease caused by mutations in PKD1 or PKD2. Metformin reduces cyst growth in mouse models of PKD1. However, metformin has not been studied in animal models of PKD2, and the cellular mechanism underlying its effectiveness is not...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5541071/ https://www.ncbi.nlm.nih.gov/pubmed/28769124 http://dx.doi.org/10.1038/s41598-017-07300-x |
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author | Chang, Ming-Yang Ma, Tsu-Lin Hung, Cheng-Chieh Tian, Ya-Chung Chen, Yung-Chang Yang, Chih-Wei Cheng, Yi-Chuan |
author_facet | Chang, Ming-Yang Ma, Tsu-Lin Hung, Cheng-Chieh Tian, Ya-Chung Chen, Yung-Chang Yang, Chih-Wei Cheng, Yi-Chuan |
author_sort | Chang, Ming-Yang |
collection | PubMed |
description | Autosomal dominant polycystic kidney disease (ADPKD) is a common kidney disease caused by mutations in PKD1 or PKD2. Metformin reduces cyst growth in mouse models of PKD1. However, metformin has not been studied in animal models of PKD2, and the cellular mechanism underlying its effectiveness is not entirely clear. This study investigated the effects of metformin on cyst formation in a zebrafish model of polycystin-2 deficiency resulting from morpholino knockdown of pkd2. We added metformin (2.5 to 20 mM) to the embryo media between 4 and 48 hours post fertilisation and observed pronephric cyst formation by using the wt1b promoter-driven GFP signal in Tg(wt1b:GFP) pkd2 morphants. Metformin inhibited pronephric cyst formation by 42–61% compared with the untreated controls. Metformin also reduced the number of proliferating cells in the pronephric ducts, the degree of dorsal body curvature, and the infiltration of leukocytes surrounding the pronephros. Moreover, metformin treatment increased the phosphorylation of adenosine monophosphate-activated protein kinase (AMPK) and enhanced autophagy in the pronephros. Our data suggest that metformin reduces cyst formation through activation of the AMPK pathway and modulation of defective cellular events such as proliferation and autophagy. These results also imply that metformin could have therapeutic potential for ADPKD treatment. |
format | Online Article Text |
id | pubmed-5541071 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55410712017-08-07 Metformin Inhibits Cyst Formation in a Zebrafish Model of Polycystin-2 Deficiency Chang, Ming-Yang Ma, Tsu-Lin Hung, Cheng-Chieh Tian, Ya-Chung Chen, Yung-Chang Yang, Chih-Wei Cheng, Yi-Chuan Sci Rep Article Autosomal dominant polycystic kidney disease (ADPKD) is a common kidney disease caused by mutations in PKD1 or PKD2. Metformin reduces cyst growth in mouse models of PKD1. However, metformin has not been studied in animal models of PKD2, and the cellular mechanism underlying its effectiveness is not entirely clear. This study investigated the effects of metformin on cyst formation in a zebrafish model of polycystin-2 deficiency resulting from morpholino knockdown of pkd2. We added metformin (2.5 to 20 mM) to the embryo media between 4 and 48 hours post fertilisation and observed pronephric cyst formation by using the wt1b promoter-driven GFP signal in Tg(wt1b:GFP) pkd2 morphants. Metformin inhibited pronephric cyst formation by 42–61% compared with the untreated controls. Metformin also reduced the number of proliferating cells in the pronephric ducts, the degree of dorsal body curvature, and the infiltration of leukocytes surrounding the pronephros. Moreover, metformin treatment increased the phosphorylation of adenosine monophosphate-activated protein kinase (AMPK) and enhanced autophagy in the pronephros. Our data suggest that metformin reduces cyst formation through activation of the AMPK pathway and modulation of defective cellular events such as proliferation and autophagy. These results also imply that metformin could have therapeutic potential for ADPKD treatment. Nature Publishing Group UK 2017-08-02 /pmc/articles/PMC5541071/ /pubmed/28769124 http://dx.doi.org/10.1038/s41598-017-07300-x Text en © The Author(s) 2017 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 Chang, Ming-Yang Ma, Tsu-Lin Hung, Cheng-Chieh Tian, Ya-Chung Chen, Yung-Chang Yang, Chih-Wei Cheng, Yi-Chuan Metformin Inhibits Cyst Formation in a Zebrafish Model of Polycystin-2 Deficiency |
title | Metformin Inhibits Cyst Formation in a Zebrafish Model of Polycystin-2 Deficiency |
title_full | Metformin Inhibits Cyst Formation in a Zebrafish Model of Polycystin-2 Deficiency |
title_fullStr | Metformin Inhibits Cyst Formation in a Zebrafish Model of Polycystin-2 Deficiency |
title_full_unstemmed | Metformin Inhibits Cyst Formation in a Zebrafish Model of Polycystin-2 Deficiency |
title_short | Metformin Inhibits Cyst Formation in a Zebrafish Model of Polycystin-2 Deficiency |
title_sort | metformin inhibits cyst formation in a zebrafish model of polycystin-2 deficiency |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5541071/ https://www.ncbi.nlm.nih.gov/pubmed/28769124 http://dx.doi.org/10.1038/s41598-017-07300-x |
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