Source:http://linkedlifedata.com/resource/pubmed/id/15536074
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions |
umls-concept:C0015576,
umls-concept:C0021467,
umls-concept:C0021469,
umls-concept:C0035820,
umls-concept:C0206364,
umls-concept:C0243102,
umls-concept:C0751984,
umls-concept:C1096978,
umls-concept:C1264638,
umls-concept:C1412517,
umls-concept:C1423613,
umls-concept:C1512810,
umls-concept:C1546857,
umls-concept:C1622501,
umls-concept:C1720675
|
pubmed:issue |
2
|
pubmed:dateCreated |
2005-1-11
|
pubmed:abstractText |
Genetic studies have shown that Eph receptor tyrosine kinases have both kinase-dependent and kinase-independent functions through incompletely understood mechanisms. We report here that ephrin-B1 stimulation of endogenous EphB kinases in LS174T colorectal epithelial cells inhibited integrin-mediated adhesion and HGF/SF-induced directional cell migration. Using 293 cells stably transfected with wild type (WT)- or kinase-deficient (KD-EphB3), we found that inhibition of integrin-mediated cell adhesion and induction of cell rounding was kinase-dependent. Unexpectedly, in two independent assays, both KD- and WT-EphB3 significantly inhibited directional cell migration. Upon ephrin-B1 stimulation, the activities of Rac1 and Cdc42 were reduced in both WT- and KD-EphB3-expressing cells that were induced to migrate. Pharmacological evidence demonstrates that a relative increase in RhoA signaling as a result of decreased Rac1/Cdc42 activities contributes to the inhibitory effects. Furthermore, EphB3-mediated inhibitory effect on cell adhesion but not migration was abolished by the integrin activating antibodies, suggesting that the inhibition of cell migration is not because of down-regulation of integrin function. These results uncover a differential requirement for EphB3 catalytic activity in the regulation of cell adhesion and migration, and suggest that while catalytic activity of EphB3 is required for inhibition of integrin-mediated cell adhesion, a distinct signaling pathway to Rho GTPases shared by WT- and KD-EphB3 receptor mediates inhibition of directional cell migration.
|
pubmed:grant | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Ephrin-B1,
http://linkedlifedata.com/resource/pubmed/chemical/Fibronectins,
http://linkedlifedata.com/resource/pubmed/chemical/Hepatocyte Growth Factor,
http://linkedlifedata.com/resource/pubmed/chemical/Integrins,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, EphB3,
http://linkedlifedata.com/resource/pubmed/chemical/rho GTP-Binding Proteins
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jan
|
pubmed:issn |
0021-9258
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
14
|
pubmed:volume |
280
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
923-32
|
pubmed:dateRevised |
2009-11-19
|
pubmed:meshHeading |
pubmed-meshheading:15536074-Catalysis,
pubmed-meshheading:15536074-Cell Adhesion,
pubmed-meshheading:15536074-Cell Line,
pubmed-meshheading:15536074-Cell Movement,
pubmed-meshheading:15536074-Cell Surface Extensions,
pubmed-meshheading:15536074-Colon,
pubmed-meshheading:15536074-Enzyme Activation,
pubmed-meshheading:15536074-Ephrin-B1,
pubmed-meshheading:15536074-Epithelial Cells,
pubmed-meshheading:15536074-Fibronectins,
pubmed-meshheading:15536074-Hepatocyte Growth Factor,
pubmed-meshheading:15536074-Humans,
pubmed-meshheading:15536074-Integrins,
pubmed-meshheading:15536074-Receptor, EphB3,
pubmed-meshheading:15536074-rho GTP-Binding Proteins
|
pubmed:year |
2005
|
pubmed:articleTitle |
Inhibition of integrin-mediated cell adhesion but not directional cell migration requires catalytic activity of EphB3 receptor tyrosine kinase. Role of Rho family small GTPases.
|
pubmed:affiliation |
Rammelkamp Center for Research, MetroHealth Campus, and Department of Pharmacology and Ireland Cancer Center, Case Western Reserve University School of Medicine, Cleveland, Ohio 44109, USA.
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, U.S. Gov't, Non-P.H.S.,
Research Support, Non-U.S. Gov't
|