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Ezrin Is a Novel Protein Partner of Aquaporin-5 in Human Salivary Glands and Shows Altered Expression and Cellular Localization in Sjögren's Syndrome


AUTHORS

Chivasso CClara , Hagströmer CJCarl Johan , Rose KLKristie L , Lhotellerie FFlorent , Leblanc LLionel , Wang ZZhen , Moscato SStefania , Chevalier CClément , Zindy EEgor , Martin MMaud , Vanhollebeke BBenoit , Gregoire FFrançoise , Bolaky NNargis , Perret JJason , Baldini CChiara , Soyfoo MSMuhammad Shahnawaz , Mattii LLetizia , Schey KLKevin L , Törnroth-Horsefield SSusanna , Delporte CChristine . International journal of molecular sciences. 2021 8 26; 22(17).

ABSTRACT

Sjögren’s syndrome (SS) is an exocrinopathy characterized by the hypofunction of salivary glands (SGs). Aquaporin-5 (AQP5); a water channel involved in saliva formation; is aberrantly distributed in SS SG acini and contributes to glandular dysfunction. We aimed to investigate the role of ezrin in AQP5 mislocalization in SS SGs. The AQP5-ezrin interaction was assessed by immunoprecipitation and proteome analysis and by proximity ligation assay in immortalized human SG cells. We demonstrated, for the first time, an interaction between ezrin and AQP5. A model of the complex was derived by computer modeling and in silico docking; suggesting that AQP5 interacts with the ezrin FERM-domain via its C-terminus. The interaction was also investigated in human minor salivary gland (hMSG) acini from SS patients (SICCA-SS); showing that AQP5-ezrin complexes were absent or mislocalized to the basolateral side of SG acini rather than the apical region compared to controls (SICCA-NS). Furthermore, in SICCA-SS hMSG acinar cells, ezrin immunoreactivity was decreased at the acinar apical region and higher at basal or lateral regions, accounting for altered AQP5-ezrin co-localization. Our data reveal that AQP5-ezrin interactions in human SGs could be involved in the regulation of AQP5 trafficking and may contribute to AQP5-altered localization in SS patients.