Zeb1 affects epithelial cell adhesion by diverting glycosphingolipid metabolism. (2nd February 2015)

• Record Type: Journal Article
• Authors: Mathow, Daniel; Chessa, Federica; Rabionet, Mariona; Kaden, Sylvia; Jennemann, Richard; Sandhoff, Roger; Gröne, Hermann‐Josef; Feuerborn, Alexander
• Is Part Of: EMBO reports. Volume 16:Number 3(2015:Mar.)
• Page Start: 321
• Page End: 331
• Publication Date: 2015-02-02
• Subjects: Molecular biology -- Periodicals; Molecular Biology -- Periodicals; Molecular biology; Periodicals; 572.8
• DOI: 10.15252/embr.201439333
• Languages: English
• ISSNs: 1469-221X

Abstract

<abstract abstract-type="main" id="embr201439333-abs-0001"> <title>Abstract</title> <p>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 (<italic>St3gal5</italic>), which mechanistically involves Zeb1 binding to the <italic>St3gal5</italic> promoter as well as suppressing microRNA‐mediated repression of <italic>St3gal5</italic>. 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.</p> </abstract>