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Essential Functions of Glycans in Human Epithelia Dissected by a CRISPR-Cas9-Engineered Human Organotypic Skin Model
The glycome undergoes characteristic changes during histogenesis and organogenesis, but our understanding of the importance of select glycan structures for tissue formation and homeostasis is incomplete. Here, we present a human organotypic platform that allows genetic dissection of cellular glycosy...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7497784/ https://www.ncbi.nlm.nih.gov/pubmed/32710848 http://dx.doi.org/10.1016/j.devcel.2020.06.039 |
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author | Dabelsteen, Sally Pallesen, Emil M.H. Marinova, Irina N. Nielsen, Mathias I. Adamopoulou, Maria Rømer, Troels B. Levann, Asha Andersen, Mikkel M. Ye, Zilu Thein, David Bennett, Eric P. Büll, Christian Moons, Sam J. Boltje, Thomas Clausen, Henrik Vakhrushev, Sergey Y. Bagdonaite, Ieva Wandall, Hans H. |
author_facet | Dabelsteen, Sally Pallesen, Emil M.H. Marinova, Irina N. Nielsen, Mathias I. Adamopoulou, Maria Rømer, Troels B. Levann, Asha Andersen, Mikkel M. Ye, Zilu Thein, David Bennett, Eric P. Büll, Christian Moons, Sam J. Boltje, Thomas Clausen, Henrik Vakhrushev, Sergey Y. Bagdonaite, Ieva Wandall, Hans H. |
author_sort | Dabelsteen, Sally |
collection | PubMed |
description | The glycome undergoes characteristic changes during histogenesis and organogenesis, but our understanding of the importance of select glycan structures for tissue formation and homeostasis is incomplete. Here, we present a human organotypic platform that allows genetic dissection of cellular glycosylation capacities and systematic interrogation of the roles of distinct glycan types in tissue formation. We used CRISPR-Cas9 gene targeting to generate a library of 3D organotypic skin tissues that selectively differ in their capacity to produce glycan structures on the main types of N- and O-linked glycoproteins and glycolipids. This tissue library revealed distinct changes in skin formation associated with a loss of features for all tested glycoconjugates. The organotypic skin model provides phenotypic cues for the distinct functions of glycoconjugates and serves as a unique resource for further genetic dissection and identification of the specific structural features involved. The strategy is also applicable to other organotypic tissue models. |
format | Online Article Text |
id | pubmed-7497784 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-74977842020-09-28 Essential Functions of Glycans in Human Epithelia Dissected by a CRISPR-Cas9-Engineered Human Organotypic Skin Model Dabelsteen, Sally Pallesen, Emil M.H. Marinova, Irina N. Nielsen, Mathias I. Adamopoulou, Maria Rømer, Troels B. Levann, Asha Andersen, Mikkel M. Ye, Zilu Thein, David Bennett, Eric P. Büll, Christian Moons, Sam J. Boltje, Thomas Clausen, Henrik Vakhrushev, Sergey Y. Bagdonaite, Ieva Wandall, Hans H. Dev Cell Resource The glycome undergoes characteristic changes during histogenesis and organogenesis, but our understanding of the importance of select glycan structures for tissue formation and homeostasis is incomplete. Here, we present a human organotypic platform that allows genetic dissection of cellular glycosylation capacities and systematic interrogation of the roles of distinct glycan types in tissue formation. We used CRISPR-Cas9 gene targeting to generate a library of 3D organotypic skin tissues that selectively differ in their capacity to produce glycan structures on the main types of N- and O-linked glycoproteins and glycolipids. This tissue library revealed distinct changes in skin formation associated with a loss of features for all tested glycoconjugates. The organotypic skin model provides phenotypic cues for the distinct functions of glycoconjugates and serves as a unique resource for further genetic dissection and identification of the specific structural features involved. The strategy is also applicable to other organotypic tissue models. Cell Press 2020-09-14 /pmc/articles/PMC7497784/ /pubmed/32710848 http://dx.doi.org/10.1016/j.devcel.2020.06.039 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Resource Dabelsteen, Sally Pallesen, Emil M.H. Marinova, Irina N. Nielsen, Mathias I. Adamopoulou, Maria Rømer, Troels B. Levann, Asha Andersen, Mikkel M. Ye, Zilu Thein, David Bennett, Eric P. Büll, Christian Moons, Sam J. Boltje, Thomas Clausen, Henrik Vakhrushev, Sergey Y. Bagdonaite, Ieva Wandall, Hans H. Essential Functions of Glycans in Human Epithelia Dissected by a CRISPR-Cas9-Engineered Human Organotypic Skin Model |
title | Essential Functions of Glycans in Human Epithelia Dissected by a CRISPR-Cas9-Engineered Human Organotypic Skin Model |
title_full | Essential Functions of Glycans in Human Epithelia Dissected by a CRISPR-Cas9-Engineered Human Organotypic Skin Model |
title_fullStr | Essential Functions of Glycans in Human Epithelia Dissected by a CRISPR-Cas9-Engineered Human Organotypic Skin Model |
title_full_unstemmed | Essential Functions of Glycans in Human Epithelia Dissected by a CRISPR-Cas9-Engineered Human Organotypic Skin Model |
title_short | Essential Functions of Glycans in Human Epithelia Dissected by a CRISPR-Cas9-Engineered Human Organotypic Skin Model |
title_sort | essential functions of glycans in human epithelia dissected by a crispr-cas9-engineered human organotypic skin model |
topic | Resource |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7497784/ https://www.ncbi.nlm.nih.gov/pubmed/32710848 http://dx.doi.org/10.1016/j.devcel.2020.06.039 |
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