The authors found that the endogenous TGFβ receptor in cultured cells localizes to endosomes containing the early endosomal marker EEA1. SARA, a soluble cytoplasmic protein required for TGFβ function, is found almost exclusively in the same EEA1-enriched endosomes. Disrupting TGFβ receptor endocytosis impairs downstream signaling events normally mediated by the receptor. This result is reminiscent of the disruption of antiapoptotic signaling recently noted in cells that lack clathrin function (Wettey, F.R., et al. 2002. Science 297:1521–1525).
This is the first time membrane trafficking has been shown to be required for the productive association of two components of a signaling pathway, and it suggests that the function of the endosome in signaling may need to be reevaluated. Hayes et al. propose two models to explain their results: either SARA and other signaling components are restricted to the endosome, requiring TGFβ receptor internalization to form the signaling complex, or the TGFβ receptor signaling complex forms at the plasma membrane, but requires the biochemical conditions of the endosome to produce a signal. ▪