The F-actin-binding RapGEF GflB is required for efficient macropinocytosis in <i>Dictyostelium</i>

Abstract

Macropinocytosis involves the uptake of large volumes of fluid, which is regulated by various small GTPases. The <i>Dictyostelium discoideum</i> protein GflB is a guanine nucleotide exchange factor (GEF) of Rap1, and is involved in chemotaxis. Here, we studied the role of GflB in macropinocytosis, phagocytosis and cytokinesis. In plate culture of vegetative cells, compared with the parental strain AX2, <i>gflB</i>-knockout (KO) cells were flatter and more polarized, whereas GflB-overproducing cells were rounder. The <i>gflB</i>-KO cells exhibited impaired crown formation and retraction, particularly retraction, resulting in more crowns (macropinocytic cups) per cell and longer crown lifetimes. Accordingly, <i>gflB</i>-KO cells showed defects in macropinocytosis and also in phagocytosis and cytokinesis. F-actin levels were elevated in <i>gflB</i>-KO cells. GflB localized to the actin cortex most prominently at crowns and phagocytic cups. The villin headpiece domain (VHP)-like N-terminal domain of GflB directly interacted with F-actin <i>in vitro</i> Furthermore, a domain enriched in basic amino acids interacted with specific membrane cortex structures such as the cleavage furrow. In conclusion, GflB acts as a key local regulator of actin-driven membrane protrusion possibly by modulating Rap1 signaling pathways.