Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/57538
Título : Protein 4.1R regulates cell migration and IQGAP1 recruitment to the leading edge
Autor : Ruiz-Saenz, Ana, Kremer, Leonor, Alonso, Miguel A., Millán, Jaime, Correas, Isabel
Palabras clave : Red blood cells
Protein
Cell migration
Protein 4.1R
IQGAP1
Fecha de publicación : 2011
Editor: Company of Biologists
Citación : Journal of Cell Science 124: 2529-2538 (2011)
Resumen: In red blood cells, multifunctional protein 4.1R stabilizes the spectrin–actin network and anchors it to the plasma membrane. To contribute to the characterization of functional roles of 4.1R in nonerythroid cells, we have analyzed the participation of protein 4.1R in cell migration. The distribution of endogenous 4.1R is polarized towards the leading edge of migrating cells. Exogenous 4.1R isoforms containing a complete membrane-binding domain consistently localized to plasma membrane extensions enriched in F-actin. Silencing of 4.1R caused the loss of persistence of migration in subconfluent cells and of directional migration in cells moving into a wound. Coimmunoprecipitation and pull-down assays identified the scaffold protein IQGAP1 as a partner for protein 4.1R and showed that the 4.1R membrane-binding domain is involved in binding IQGAP1. Importantly, we show that protein 4.1R is necessary for the localization of IQGAP1 to the leading edge of cells migrating into a wound, whereas IQGAP1 is not required for protein 4.1R localization. Collectively, our results indicate a crucial role for protein 4.1R in cell migration and in the recruitment of the scaffold protein IQGAP1 to the cell front.
Versión del editor: http://dx.doi.org/10.1242/​jcs.083634
URI : http://hdl.handle.net/10261/57538
ISSN: 0021-9533
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