Persistent cell migration and adhesion rely on retrograde transport of β1 integrin

Integrins have key functions in cell adhesion and migration. How integrins are dynamically relocalized to the leading edge in highly polarized migratory cells has remained unexplored. Here, we demonstrate that β 1 integrin (known as PAT-3 in Caenorhabditis elegans ), but not β 3 , is transported from the plasma membrane to the trans -Golgi network, to be resecreted in a polarized manner. This retrograde trafficking is restricted to the non-ligand-bound conformation of β 1 integrin. Retrograde trafficking inhibition abrogates several β 1 -integrin-specific functions such as cell adhesion in early embryonic development of mice, and persistent cell migration in the developing posterior gonad arm of C. elegans . Our results establish a paradigm according to which retrograde trafficking, and not endosomal recycling, is the key driver for β 1 integrin function in highly polarized cells. These data more generally suggest that the retrograde route is used to relocalize plasma membrane machinery from previous sites of function to the leading edge of migratory cells. Johannes and colleagues report that retrograde trafficking of non-liganded β 1 integrin from the plasma membrane to the trans -Golgi network to then be secreted in a polarized manner is needed for cell adhesion and persistent migration.