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Dermatan sulfate epimerase 1 deficient mice as a model for human abdominal wall defects

BACKGROUND: Dermatan sulfate (DS) is a highly sulfated polysaccharide with a variety of biological functions in extracellular matrix organization and processes such as tumorigenesis and wound healing. A distinct feature of DS is the presence of iduronic acid, produced by the two enzymes, DS-epimeras...

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Autores principales: Gustafsson, Renata, Stachtea, Xanthi, Maccarana, Marco, Grottling, Emma, Eklund, Erik, Malmström, Anders, Oldberg, Åke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4233991/
https://www.ncbi.nlm.nih.gov/pubmed/25186462
http://dx.doi.org/10.1002/bdra.23300
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author Gustafsson, Renata
Stachtea, Xanthi
Maccarana, Marco
Grottling, Emma
Eklund, Erik
Malmström, Anders
Oldberg, Åke
author_facet Gustafsson, Renata
Stachtea, Xanthi
Maccarana, Marco
Grottling, Emma
Eklund, Erik
Malmström, Anders
Oldberg, Åke
author_sort Gustafsson, Renata
collection PubMed
description BACKGROUND: Dermatan sulfate (DS) is a highly sulfated polysaccharide with a variety of biological functions in extracellular matrix organization and processes such as tumorigenesis and wound healing. A distinct feature of DS is the presence of iduronic acid, produced by the two enzymes, DS-epimerase 1 and 2, which are encoded by Dse and Dsel, respectively. METHODS: We have previously shown that Dse knockout (KO) mice in a mixed C57BL/6–129/SvJ background have an altered collagen matrix structure in skin. In the current work we studied Dse KO mice in a pure NFR genetic background. RESULTS: Dse KO embryos and newborns had kinked tails and histological staining revealed significantly thicker epidermal layers in Dse KO mice when compared with heterozygote (Het) or wild-type (WT) littermates. Immunochemical analysis of the epidermal layers in newborn pups showed increased expression of keratin 5 in the basal layer and keratin 1 in the spinous layer. In addition, we observed an abdominal wall defect with herniated intestines in 16% of the Dse KO embryos. Other, less frequent, developmental defects were exencephaly and spina bifida. CONCLUSION: We conclude that the combination of defective collagen structure in the dermis and imbalanced keratinocyte maturation could be responsible for the observed developmental defects in Dse KO mice. In addition, we propose that Dse KO mice could be used as a model in pathogenetic studies of human fetal abdominal wall defects. Birth Defects Research (Part A) 100:712–720, 2014. © 2014 Wiley Periodicals, Inc.
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spelling pubmed-42339912014-12-03 Dermatan sulfate epimerase 1 deficient mice as a model for human abdominal wall defects Gustafsson, Renata Stachtea, Xanthi Maccarana, Marco Grottling, Emma Eklund, Erik Malmström, Anders Oldberg, Åke Birth Defects Res A Clin Mol Teratol Original Research Article BACKGROUND: Dermatan sulfate (DS) is a highly sulfated polysaccharide with a variety of biological functions in extracellular matrix organization and processes such as tumorigenesis and wound healing. A distinct feature of DS is the presence of iduronic acid, produced by the two enzymes, DS-epimerase 1 and 2, which are encoded by Dse and Dsel, respectively. METHODS: We have previously shown that Dse knockout (KO) mice in a mixed C57BL/6–129/SvJ background have an altered collagen matrix structure in skin. In the current work we studied Dse KO mice in a pure NFR genetic background. RESULTS: Dse KO embryos and newborns had kinked tails and histological staining revealed significantly thicker epidermal layers in Dse KO mice when compared with heterozygote (Het) or wild-type (WT) littermates. Immunochemical analysis of the epidermal layers in newborn pups showed increased expression of keratin 5 in the basal layer and keratin 1 in the spinous layer. In addition, we observed an abdominal wall defect with herniated intestines in 16% of the Dse KO embryos. Other, less frequent, developmental defects were exencephaly and spina bifida. CONCLUSION: We conclude that the combination of defective collagen structure in the dermis and imbalanced keratinocyte maturation could be responsible for the observed developmental defects in Dse KO mice. In addition, we propose that Dse KO mice could be used as a model in pathogenetic studies of human fetal abdominal wall defects. Birth Defects Research (Part A) 100:712–720, 2014. © 2014 Wiley Periodicals, Inc. BlackWell Publishing Ltd 2014-09 2014-09-04 /pmc/articles/PMC4233991/ /pubmed/25186462 http://dx.doi.org/10.1002/bdra.23300 Text en © 2014 Wiley Periodicals, Inc.
spellingShingle Original Research Article
Gustafsson, Renata
Stachtea, Xanthi
Maccarana, Marco
Grottling, Emma
Eklund, Erik
Malmström, Anders
Oldberg, Åke
Dermatan sulfate epimerase 1 deficient mice as a model for human abdominal wall defects
title Dermatan sulfate epimerase 1 deficient mice as a model for human abdominal wall defects
title_full Dermatan sulfate epimerase 1 deficient mice as a model for human abdominal wall defects
title_fullStr Dermatan sulfate epimerase 1 deficient mice as a model for human abdominal wall defects
title_full_unstemmed Dermatan sulfate epimerase 1 deficient mice as a model for human abdominal wall defects
title_short Dermatan sulfate epimerase 1 deficient mice as a model for human abdominal wall defects
title_sort dermatan sulfate epimerase 1 deficient mice as a model for human abdominal wall defects
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4233991/
https://www.ncbi.nlm.nih.gov/pubmed/25186462
http://dx.doi.org/10.1002/bdra.23300
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