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Endoglin controls cell migration and composition of focal adhesions: function of the cytosolic domain.

Authors: Conley, Barbara A.; Koleva, Rositsa; Smith, Joshua D.; Kacer, Doreen; Zhang, Dongwang; Bernabéu, Carmelo; Vary, Calvin P. H.;

Endoglin controls cell migration and composition of focal adhesions: function of the cytosolic domain.

Abstract

Mutations in the human endoglin gene result in hereditary hemorrhagic telangiectasia type 1, a vascular disorder characterized by multisystemic vascular dysplasia, arteriovenous malformations, and focal dilatation of postcapillary venules. Previous studies have implicated endoglin in the inhibition of cell migration in vivo and in vitro. In the course of studies to address the relationship of the conserved cytosolic domain to endoglin function, we identified zyxin, a LIM domain protein that is concentrated at focal adhesions, as an interactor with endoglin in human umbilical vein vascular endothelial cells. This interaction is localized within the 47-amino acid carboxyl-terminal cytosolic domain of endoglin, and maps within zyxin residues 326–572. The endoglin-zyxin interaction was found to be largely mediated by the third LIM domain of zyxin, and is specific for endoglin because the homologous cytosolic domain of the transforming growth factor-β type III receptor, betaglycan, fails to interact with zyxin. Expression of endoglin is associated with reduction of zyxin, as well as its interacting proteins p130cas and CrkII, from a focal adhesion protein fraction, and this reduction is correlated with inhibition of cell migration. We also show that endoglin-dependent: (i) inhibition of cell migration, (ii) reduction of focal adhesion-associated p130cas/CrkII protein levels, (iii) tyrosine phosphorylation of p130cas, and (iv) focal adhesion-associated endoglin levels are mediated by the cytosolic domain of endoglin. These results suggest a novel mechanism of endoglin function involving its interaction with LIM domain-containing proteins, and associated adapter proteins, affecting sites of focal adhesion

This work was supported by National Institutes of Health Grant P20 15555 from the COBRE program of the National Center for Research Resources. The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked “advertisement” in accordance with 18 U.S.C. Section 1734 solely to indicate this fact

10 páginas, 7 figuras -- PAGS nros. 27440-27449

Peer reviewed

Keywords

Focal Adhesions, Endoglin, Receptors, Cell Surface, Microspheres, Cell Line, Protein Structure, Tertiary, Cytoskeletal Proteins, Mice, Cytosol, Microscopy, Fluorescence, Antigens, CD, Cell Movement, Mutagenesis, Site-Directed, Animals, Humans, Phosphorylation, Oligopeptides, Gene Deletion, Glycoproteins, Protein Binding

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
123
Top 10%
Top 10%
Top 1%
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gold