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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BlackWell Publishing Ltd
2014
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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. |
format | Online Article Text |
id | pubmed-4233991 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BlackWell Publishing Ltd |
record_format | MEDLINE/PubMed |
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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