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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.
Affiliation
  • Dabelsteen S; Copenhagen Center for Glycomics, Department of Cellular and Molecular Medicine, University of Copenhagen, Copenhagen, Denmark; Department of Oral Pathology, School of Dentistry, University of Copenhagen, Denmark.
  • Pallesen EMH; Copenhagen Center for Glycomics, Department of Cellular and Molecular Medicine, University of Copenhagen, Copenhagen, Denmark.
  • Marinova IN; Copenhagen Center for Glycomics, Department of Cellular and Molecular Medicine, University of Copenhagen, Copenhagen, Denmark.
  • Nielsen MI; Copenhagen Center for Glycomics, Department of Cellular and Molecular Medicine, University of Copenhagen, Copenhagen, Denmark.
  • Adamopoulou M; Department of Oral Pathology, School of Dentistry, University of Copenhagen, Denmark.
  • Rømer TB; Copenhagen Center for Glycomics, Department of Cellular and Molecular Medicine, University of Copenhagen, Copenhagen, Denmark.
  • Levann A; Copenhagen Center for Glycomics, Department of Cellular and Molecular Medicine, University of Copenhagen, Copenhagen, Denmark.
  • Andersen MM; Copenhagen Center for Glycomics, Department of Cellular and Molecular Medicine, University of Copenhagen, Copenhagen, Denmark.
  • Ye Z; Copenhagen Center for Glycomics, Department of Cellular and Molecular Medicine, University of Copenhagen, Copenhagen, Denmark.
  • Thein D; Copenhagen Center for Glycomics, Department of Cellular and Molecular Medicine, University of Copenhagen, Copenhagen, Denmark.
  • Bennett EP; Copenhagen Center for Glycomics, Department of Cellular and Molecular Medicine, University of Copenhagen, Copenhagen, Denmark.
  • Büll C; Copenhagen Center for Glycomics, Department of Cellular and Molecular Medicine, University of Copenhagen, Copenhagen, Denmark.
  • Moons SJ; Institute for Molecules and Materials, Nijmegen 6525 AJ, the Netherlands.
  • Boltje T; Institute for Molecules and Materials, Nijmegen 6525 AJ, the Netherlands.
  • Clausen H; Copenhagen Center for Glycomics, Department of Cellular and Molecular Medicine, University of Copenhagen, Copenhagen, Denmark.
  • Vakhrushev SY; Copenhagen Center for Glycomics, Department of Cellular and Molecular Medicine, University of Copenhagen, Copenhagen, Denmark.
  • Bagdonaite I; Copenhagen Center for Glycomics, Department of Cellular and Molecular Medicine, University of Copenhagen, Copenhagen, Denmark.
  • Wandall HH; Copenhagen Center for Glycomics, Department of Cellular and Molecular Medicine, University of Copenhagen, Copenhagen, Denmark. Electronic address: hhw@sund.ku.dk.
Dev Cell ; 54(5): 669-684.e7, 2020 09 14.
Article in En | MEDLINE | ID: mdl-32710848
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.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polysaccharides / Epithelium / Clustered Regularly Interspaced Short Palindromic Repeats / CRISPR-Cas Systems Type of study: Prognostic_studies Limits: Humans Language: En Journal: Dev Cell Journal subject: EMBRIOLOGIA Year: 2020 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Polysaccharides / Epithelium / Clustered Regularly Interspaced Short Palindromic Repeats / CRISPR-Cas Systems Type of study: Prognostic_studies Limits: Humans Language: En Journal: Dev Cell Journal subject: EMBRIOLOGIA Year: 2020 Document type: Article Affiliation country: Country of publication: