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I. and tissue homeostasis. In response to its ligand, hepatocyte YM348 growth factor (HGF), Met coordinates the dynamic polarization of cells by regulating formation of cell protrusions, actin cytoskeleton remodeling, and formation and turnover of focal adhesions (FAs; Gherardi et al., 2012). Dysregulated Met signaling contributes to tumor progression by promoting tumor cell survival, as well as cell migration and invasion (Lai et al., 2009). However, the mechanisms through which Met regulates cell motility and cytoskeleton dynamics remain poorly understood. Arf6, the least conserved member of the Arf family of GTPases, belongs to the Ras GTPase superfamily and localizes to the plasma membrane (PM) and endosomal compartments (DSouza-Schorey and Chavrier, 2006). Arf6 is activated downstream from Met (Palacios and DSouza-Schorey, 2003; Miura et al., 2017) and regulates endocytic membrane trafficking (Gillingham and Munro, 2007; Grossmann et al., 2019), including the Met RTK (Parachoniak et al., 2011). Arf6 also regulates the remodeling of actin cytoskeleton and FA dynamics to control cell motility (DSouza-Schorey et al., 1997; Radhakrishna and Donaldson, 1997; Matsumoto et al., 2017). One role for Arf6 in cell migration is mediated through the regulation of members of the Rho family of small GTPases, either Rac1 (Boshans et al., 2000; Cotton et al., 2007) or Cdc42 (Osmani et al., 2010). However, the detailed mechanisms for Arf6 influence on cell motility downstream from Met remain elusive. Rho GTPases are crucial regulators of the actin cytoskeleton rearrangements and FA dynamics (Ridley et al., 2003). They function as molecular switches and interact with downstream effector molecules to propagate the signal transduction in their GTP-loaded state (Bourne et al., 1991). They are required for effective cell migration and invasion (Ridley et al., 2003) as well as cell proliferation, apoptosis, and mitosis (Spiering and Hodgson, 2011). Although there are 20 human Rho GTPases, only a few have been studied downstream of Met despite their involvement in cell migration. To date, a role for Rac1, Cdc42, and RhoA in regulating cell migration downstream from Met has been identified (Takaishi et al., 1994; Royal et al., 2000; Lamorte et al., 2002), but involvement of other members, such as RhoB, has not been established. The Rho family of GTPases includes the three isoforms RhoA, RhoB, and RhoC, which are 85% identical in sequence, with most differences concentrated in the C-terminus. Prenylation at the C-terminus is crucial for their function in cell growth, oncogenic transformation, and cytoskeleton organization, as well as their localization and stability (Wheeler and Ridley, 2004). Rho GTPases are generally localized in the cytoplasm and, in response to stimuli, translocate to the PM. Notably, RhoB is also present in the endosomes (Mellor et al., 1998; Wheeler and Ridley, 2004; Wherlock et al., 2004; Rondanino et al., 2007), multivesicular bodies, and nucleus (Ju and Gilkes, 2018). RhoB has been implicated in the regulation of epidermal Rabbit polyclonal to TDGF1 growth factor receptor and platelet-derived growth factor receptor= 20). (C) Endogenous RhoB coprecipitated with endogenous Arf6 of YM348 HeLa cells, which were lysed and subjected to immunoprecipitation (IP) and analyzed by immunoblotting. (D) In vitro GST pull-down assay of purified RhoA or RhoB with purified Arf6, loaded with GDP or GTPS. (E) HeLa cells were cotransfected with Arf6-HA (WT), Arf6-HA (DA), or Arf6-HA (DN); lysed; and subjected to IP with RhoB-GFP (WT) and Western blotted as shown. (F) HeLa cells were cotransfected with RhoB-HA (WT), RhoB-HA (DA), and RhoB-HA (DN), lysed, YM348 and subjected to IP with Arf6-GFP (WT) and Western blotted as shown. (G) HeLa cells transfected with GFP-RhoB (WT), GFP-RhoB (DA), GFP-RhoB (DN), or GFP-GGA3 were lysed and subjected to IP with an anti-GFP antibody; protein complexes were separated by SDS-PAGE and transferred to nitrocellulose membranes. The membranes were incubated with fusion protein GST alone or GST-Arf6 and immunoblotted. (H) In vitro binding assay with purified recombinant proteins. GST-RhoB (WT), GST-RhoB (DA), or GST-RhoB (DN) in the presence or absence of His-Arf6, subjected to a GST pull-down and Western blot as shown. (I) Schematic of Arf6 mutant constructs. (J) GST, GST-Arf6, GST-Arf6 28C175, and GST-Arf6 73C175 were transfected into.