摘要：SummaryRab proteins are well known regulators of intracellular trafficking; however, more and more studies point to their function also in other cellular processes, including cell migration. In this work, we have performed an siRNA screen to identify Rab proteins that influence cell migration. The screen revealed Rab33b as the strongest candidate that affected cell motility. Rab33b has been previously reported to localize at the Golgi apparatus to regulate Golgi-to-ER retrograde trafficking and Golgi homeostasis. We revealed that Rab33b also mediates post-Golgi transport to the plasma membrane. We further identified Exoc6, a subunit of the exocyst complex, as an interactor of Rab33b. Moreover, our data indicate that Rab33b regulates focal adhesion dynamics by modulating the delivery of cargo such as integrins to focal adhesions. Altogether, our results demonstrate a role for Rab33b in cell migration by regulating the delivery of integrins to focal adhesions through the interaction with Exoc6.Graphical abstractDisplay OmittedHighlights•RNAi screen reveals a role for Rab33b in cell migration•Rab33b influences focal adhesion dynamics•Rab33b interacts with the exocyst subunit Exoc6•Rab33b together with Exoc6 mediates the delivery of β1 integrin to adhesion pointsCell biology; Organizational aspects of cell biology; Functional aspects of cell biology;
