Epidermal growth factor‐induced cellular invasion requires sphingosine‐1‐phosphate/sphingosine‐1‐phosphate 2 receptor‐mediated ezrin activation. Issue 8 (29th April 2013)

• Record Type: Journal Article
• Authors: Gandy, K. Alexa Orr; Adada, Mohamad; Canals, Daniel; Carroll, Brittany; Roddy, Patrick; Hannun, Yusuf A.; Obeid, Lina M.
• Is Part Of: FASEB journal. Volume 27:Issue 8(2013)
• Page Start: 3155
• Page End: 3166
• Publication Date: 2013-04-29
• Subjects: radixin -- moesin -- actin cytoskeleton -- polarization; Biology -- Periodicals; Biology, Experimental -- Periodicals; 570
• DOI: 10.1096/fj.13-228460
• Languages: English
• ISSNs: 0892-6638

Abstract

Abstract : Ezrin, radixin, and moesin (ERM) proteins link cortical actin to the plasma membrane and coordinate cellular events that require cytoskeletal rearrangement, including cell division, migration, and invasion. While ERM proteins are involved in many important cellular events, the mechanisms regulating their function are not completely understood. Our laboratory previously identified reciprocal roles for the sphingolipids ceramide and sphingosine‐1‐phosphate (S1P) in the regulation of ERM proteins. We recently showed that ceramide‐induced activation of PP1α leads to dephosphorylation and inactivation of ERM proteins, while S1P results in phosphorylation and activation of ERM proteins. Following these findings, we aimed to examine known inducers of the SK/S1P pathway and evaluate their ability to regulate ERM proteins. We examined EGF, a known inducer of the SK/S1P pathway, for its ability to regulate the ERM family of proteins. We found that EGF induces ERM c‐terminal threonine phosphorylation via activation of the SK/S1P pathway, as this was prevented by siRNA knockdown or pharmacological inhibition of SK. Using pharmacological, as well as genetic, knockdown approaches, we determined that EGF induces ERM phosphorylation via activation of S1PR2. In addition, EGF led to cell polarization in the form of lamellipodia, and this occurred through a mechanism involving S1PR2‐mediated phosphorylation of ezrin T567. EGF‐induced cellular invasion was also found to be dependent on S1PR2‐induced T567 ezrin phosphorylation, such that S1PR2 antagonist, JTE‐013, and expression of a dominant‐negative ezrin mutant prevented cellular invasion toward EGF. In this work, a novel mechanism of EGF‐stimulated invasion is unveiled, whereby S1P‐mediated activation of S1PR2 and phosphorylation of ezrin T567 is required.—Orr Gandy, K. A., Adada, M., Canals, D., Carroll, B., Roddy, P., Hannun, Y. A.Obeid, L. M., Epidermal growth factor‐induced cellular invasion requires sphingosine‐1‐phosphate/sphingosine‐1‐phosphate 2 receptor‐mediated ezrin activation. FASEB J. 27, 3155–3166 (2013). www.fasebj.org