Actin polymerization controls the activation of multidrug efflux at fertilization by translocation and fine-scale positioning of ABCB1 on microvilli

• DOI: 10.1091/mbc.e12-06-0438
• Publication Date: 2012-08-02T00:42:33Z
• Authors: Kristen Whalen; Adam M. Reitzel; Amro Hamdoun
• Keywords: Male; 0301 basic medicine; Cytochalasin D; Embryo, Nonmammalian; Microscopy, Confocal; Microvilli; Blotting, Western; Cell Membrane; Biological Transport; Articles; Bridged Bicyclo Compounds, Heterocyclic; Actins; Polymerization; Protein Transport; 03 medical and health sciences; Microscopy, Fluorescence; Depsipeptides; Fertilization; Animals; Female; ATP Binding Cassette Transporter, Subfamily B, Member 1; Phylogeny; Ovum

Fertilization changes the structure and function of the cell surface. In sea urchins, these changes include polymerization of cortical actin and a coincident, switch-like increase in the activity of the multidrug efflux transporter ABCB1a. However, it is not clear how cortical reorganization leads to changes in membrane transport physiology. In this study, we used three-dimensional superresolution fluorescence microscopy to resolve the fine-scale movements of the transporter along polymerizing actin filaments, and we show that efflux activity is established after ABCB1a translocates to the tips of the microvilli. Inhibition of actin poly­merization or bundle formation prevents tip localization, resulting in the patching of ABCB1a at the cell surface and decreased efflux activity. In contrast, enhanced actin polymerization promotes tip localization. Finally, interference with Rab11, a regulator of apical recycling, inhibits activation of efflux activity in embryos. Together our results show that actin-mediated, short-range traffic and positioning of transporters at the cell surface regulates multidrug efflux activity and highlight the multifaceted roles of microvilli in the spatial distribution of membrane proteins.