
The microvillus brush border at the apex of the highly polarized enterocyte allows the regulated uptake of nutrients from the intestinal lumen. Here, we identify the small G protein Rap2A as a molecular link that couples the formation of microvilli directly to the preceding cell polarization. Establishment of apicobasal polarity, which can be triggered by the kinase LKB1 in single, isolated colon cells, results in enrichment of PtdIns(4,5)P(2) at the apical membrane. The subsequent recruitment of phospholipase D1 allows polarized accumulation of phosphatidic acid, which provides a local cue for successive signalling by the guanine nucleotide exchange factor PDZGEF, the small G protein Rap2A, its effector TNIK, the kinase MST4 and, ultimately, the actin-binding protein Ezrin. Thus, epithelial cell polarization is translated directly into the acquisition of brush borders through a small G protein signalling module whose action is positioned by a cortical lipid cue.
Microvilli, Cell Polarity, Protein Serine-Threonine Kinases, Real-Time Polymerase Chain Reaction, Cell Line, Germinal Center Kinases, Cytoskeletal Proteins, HEK293 Cells, rap GTP-Binding Proteins, Animals, Humans, Caco-2 Cells, Intestinal Mucosa, Caenorhabditis elegans, Cells, Cultured
Microvilli, Cell Polarity, Protein Serine-Threonine Kinases, Real-Time Polymerase Chain Reaction, Cell Line, Germinal Center Kinases, Cytoskeletal Proteins, HEK293 Cells, rap GTP-Binding Proteins, Animals, Humans, Caco-2 Cells, Intestinal Mucosa, Caenorhabditis elegans, Cells, Cultured
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