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Robo4 is a vascular-specific receptor that inhibits endothelial migration

Guidance and patterning of axons are orchestrated by cell-surface receptors and ligands that provide directional cues. Interactions between the Robo receptor and Slit ligand families of proteins initiate signaling cascades that repel axonal outgrowth. Although the vascular and nervous systems grow a...

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Published in:Developmental biology 2003-09, Vol.261 (1), p.251-267
Main Authors: Park, Kye Won, Morrison, Clayton M, Sorensen, Lise K, Jones, Christopher A, Rao, Yi, Chien, Chi-Bin, Wu, Jane Y, Urness, Lisa D, Li, Dean Y
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cited_by cdi_FETCH-LOGICAL-c460t-7238ac5b6a5d597b4a673d68b7181ea9244ffac99ac48649068a498e891e3cad3
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container_end_page 267
container_issue 1
container_start_page 251
container_title Developmental biology
container_volume 261
creator Park, Kye Won
Morrison, Clayton M
Sorensen, Lise K
Jones, Christopher A
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Urness, Lisa D
Li, Dean Y
description Guidance and patterning of axons are orchestrated by cell-surface receptors and ligands that provide directional cues. Interactions between the Robo receptor and Slit ligand families of proteins initiate signaling cascades that repel axonal outgrowth. Although the vascular and nervous systems grow as parallel networks, the mechanisms by which the vascular endothelial cells are guided to their appropriate positions remain obscure. We have identified a putative Robo homologue, Robo4, based on its differential expression in mutant mice with defects in vascular sprouting. In contrast to known neuronal Robo family members, the arrangement of the extracellular domains of Robo4 diverges significantly from that of all other Robo family members. Moreover, Robo4 is specifically expressed in the vascular endothelium during murine embryonic development. We show that Robo4 binds Slit and inhibits cellular migration in a heterologous expression system, analogous to the role of known Robo receptors in the nervous system. Immunoprecipitation studies indicate that Robo4 binds to Mena, a known effector of Robo-Slit signaling. Finally, we show that Robo4 is the only Robo family member expressed in primary endothelial cells and that application of Slit inhibits their migration. These data demonstrate that Robo4 is a bona fide member of the Robo family and may provide a repulsive cue to migrating endothelial cells during vascular development.
doi_str_mv 10.1016/S0012-1606(03)00258-6
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Immunoprecipitation studies indicate that Robo4 binds to Mena, a known effector of Robo-Slit signaling. Finally, we show that Robo4 is the only Robo family member expressed in primary endothelial cells and that application of Slit inhibits their migration. These data demonstrate that Robo4 is a bona fide member of the Robo family and may provide a repulsive cue to migrating endothelial cells during vascular development.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>12941633</pmid><doi>10.1016/S0012-1606(03)00258-6</doi><tpages>17</tpages><oa>free_for_read</oa></addata></record>
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identifier ISSN: 0012-1606
ispartof Developmental biology, 2003-09, Vol.261 (1), p.251-267
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subjects Activin receptor-like kinase 1 (Alk1)
Activin Receptors, Type I - deficiency
Activin Receptors, Type I - genetics
Activin Receptors, Type I - physiology
Activin Receptors, Type II
Amino Acid Sequence
Angiogenesis
Animals
Cell Line
Cell Movement
Chromosome Mapping
Endothelial migration
Endothelium, Vascular - embryology
Gene Expression Regulation, Developmental
HHT
Humans
In Situ Hybridization
Intercellular Signaling Peptides and Proteins
Ligands
Mice
Mice, Knockout
Molecular Sequence Data
Nerve Tissue Proteins - metabolism
Neuronal/vascular guidance
Phylogeny
Receptors, Immunologic - chemistry
Receptors, Immunologic - genetics
Receptors, Immunologic - physiology
RNA, Messenger - genetics
RNA, Messenger - metabolism
Roundabout (Robo)
Roundabout Proteins
Sequence Homology, Amino Acid
Signal Transduction
Slit
Vascular development
Vascular patterning
Vascular sprouting
Zebrafish
title Robo4 is a vascular-specific receptor that inhibits endothelial migration
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