| Literature DB >> 26272915 |
Bhuminder Singh1, Galina Bogatcheva2, Alina Starchenko3, Justine Sinnaeve4, Lynne A Lapierre5, Janice A Williams6, James R Goldenring7, Robert J Coffey8.
Abstract
Directed delivery of EGF receptor (EGFR) ligands to the apical or basolateral surface is a crucial regulatory step in the initiation of EGFR signaling in polarized epithelial cells. Herein, we show that the EGFR ligand betacellulin (BTC) is preferentially sorted to the basolateral surface of polarized MDCK cells. By using sequential truncations and site-directed mutagenesis within the BTC cytoplasmic domain, combined with selective cell-surface biotinylation and immunofluorescence, we have uncovered a monoleucine-based basolateral-sorting motif (EExxxL, specifically (156)EEMETL(161)). Disruption of this sorting motif led to equivalent apical and basolateral localization of BTC. Unlike other EGFR ligands, BTC mistrafficking induced formation of lateral lumens in polarized MDCK cells, and this process was significantly attenuated by inhibition of EGFR. Additionally, expression of a cancer-associated somatic BTC mutation (E156K) led to BTC mistrafficking and induced lateral lumens in MDCK cells. Overexpression of BTC, especially mistrafficking forms, increased the growth of MDCK cells. These results uncover a unique role for BTC mistrafficking in promoting epithelial reorganization.Entities:
Keywords: Betacellulin; EGFR signaling; Epithelial polarity; Lateral lumens; MDCK cells; Polarized trafficking
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Year: 2015 PMID: 26272915 PMCID: PMC4582402 DOI: 10.1242/jcs.170852
Source DB: PubMed Journal: J Cell Sci ISSN: 0021-9533 Impact factor: 5.285