| Literature DB >> 25643708 |
Daniel Mathow1, Federica Chessa1, Mariona Rabionet2, Sylvia Kaden1, Richard Jennemann1, Roger Sandhoff2, Hermann-Josef Gröne3, Alexander Feuerborn4.
Abstract
This study proposes that the transcription factor Zeb1 modulates epithelial cell adhesion by diverting glycosphingolipid metabolism. Zeb1 promotes expression of a-series glycosphingolipids via regulating expression of GM3 synthase (St3gal5), which mechanistically involves Zeb1 binding to the St3gal5 promoter as well as suppressing microRNA-mediated repression of St3gal5. Functionally, the repression of St3gal5 suffices to elevate intercellular adhesion and expression of distinct junction-associated proteins, reminiscent of knockdown of Zeb1. Conversely, overexpressing St3gal5 sensitizes cells towards TGF-β1-induced disruption of cell-cell interaction and partially antagonizes elevation of intercellular adhesion imposed by Zeb1 knockdown. These results highlight a direct connection of glycosphingolipid metabolism and epithelial cell adhesion via Zeb1.Entities:
Keywords: EMT; TGF‐β1; Zeb1; adhesion; glycosphingolipids
Mesh:
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Year: 2015 PMID: 25643708 PMCID: PMC4364871 DOI: 10.15252/embr.201439333
Source DB: PubMed Journal: EMBO Rep ISSN: 1469-221X Impact factor: 8.807