Abstract
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.
| Originalsprog | Engelsk |
|---|---|
| Tidsskrift | Developmental Cell |
| Vol/bind | 54 |
| Udgave nummer | 5 |
| Sider (fra-til) | 669-684.e7 |
| ISSN | 1534-5807 |
| DOI | |
| Status | Udgivet - 14 sep. 2020 |
| Udgivet eksternt | Ja |
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