Rab22a regulates the establishment of epithelial polarity

• Published in: Small GTPases Vol. 12; no. 4; pp. 282 - 293
• Main Authors: Blum, Isabella R., Behling-Hess, Caroline, Padilla-Rodriguez, Marco, Momtaz, Samina, Cox, Christopher, Wilson, Jean M.
• Format: Journal Article
• Language: English
• Published: United States Taylor & Francis 04-07-2021
• Subjects: ADP-Ribosylation Factor 6 - genetics; ADP-Ribosylation Factor 6 - metabolism; Animals; apical membrane initiation site; Arf6; Cell Membrane - metabolism; Cell Polarity; Dogs; Efa6; Endocytosis; Endosomes - metabolism; Epithelial Cells - cytology; Epithelial Cells - physiology; Guanine Nucleotide Exchange Factors - genetics; Guanine Nucleotide Exchange Factors - metabolism; HEK293 Cells; Humans; Madin Darby Canine Kidney Cells; membrane trafficking; multi-lumen; polarity; Protein Transport; rab GTP-Binding Proteins - genetics; rab GTP-Binding Proteins - metabolism; Rab14; Rab22a; Research Paper; multi-lumen; apical membrane initiation site; Efa6; Rab14; Arf6; membrane trafficking; Rab22a; polarity
• ISSN: 2154-1248; 2154-1256
• DOI: 10.1080/21541248.2020.1754104

Membrane trafficking establishes and maintains epithelial polarity. Rab22a has a polarized distribution in activated T-cells, but its role in epithelial polarity has not been investigated. We showed previously that Rab14 acts upstream of Arf6 to establish the apical membrane initiation site (AMIS), but its interaction with Rab22a is unknown. Here we show that Rab14 and Rab22a colocalize in endosomes of both unpolarized and polarized MDCK cells and Rab22a localizes to the cell:cell interface of polarizing cell pairs. Knockdown of Rab22a results in a multi-lumen phenotype in three-dimensional culture. Further, overexpression of Rab22a in Rab14 knockdown cells rescues the multi-lumen phenotype observed with Rab14 knockdown, suggesting that Rab22a is downstream of Rab14. Because of the relationship between Rab14 and Arf6, we investigated the effect of Rab22a knockdown on Arf6. We find that Rab22a knockdown results in decreased active Arf6 and that Rab22a co-immunoprecipitates with the Arf6 GEF EFA6. In addition, EFA6 is retained in intracellular puncta in Rab22a KD cells. These results suggest that Rab22a acts downstream of Rab14 to traffic EFA6 to the AMIS to regulate Arf6 in the establishment of polarity.