| pubmed-article:11580899 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:11580899 | lifeskim:mentions | umls-concept:C0037083 | lld:lifeskim |
| pubmed-article:11580899 | lifeskim:mentions | umls-concept:C0174307 | lld:lifeskim |
| pubmed-article:11580899 | lifeskim:mentions | umls-concept:C1710082 | lld:lifeskim |
| pubmed-article:11580899 | lifeskim:mentions | umls-concept:C2753224 | lld:lifeskim |
| pubmed-article:11580899 | pubmed:issue | 6 | lld:pubmed |
| pubmed-article:11580899 | pubmed:dateCreated | 2001-10-2 | lld:pubmed |
| pubmed-article:11580899 | pubmed:abstractText | We previously reported that the cell surface proteoglycan syndecan-2 can induce dendritic spine formation in hippocampal neurons. We demonstrate here that the EphB2 receptor tyrosine kinase phosphorylates syndecan-2 and that this phosphorylation event is crucial for syndecan-2 clustering and spine formation. Syndecan-2 is tyrosine phosphorylated and forms a complex with EphB2 in mouse brain. Dominant-negative inhibition of endogenous EphB receptor activities blocks clustering of endogenous syndecan-2 and normal spine formation in cultured hippocampal neurons. This is the first evidence that Eph receptors play a physiological role in dendritic spine morphogenesis. Our observations suggest that spine morphogenesis is triggered by the activation of Eph receptors, which causes tyrosine phosphorylation of target molecules, such as syndecan-2, in presumptive spines. | lld:pubmed |
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| pubmed-article:11580899 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:11580899 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:11580899 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:11580899 | pubmed:month | Sep | lld:pubmed |
| pubmed-article:11580899 | pubmed:issn | 0896-6273 | lld:pubmed |
| pubmed-article:11580899 | pubmed:author | pubmed-author:YamaguchiYY | lld:pubmed |
| pubmed-article:11580899 | pubmed:author | pubmed-author:CouchmanJ RJR | lld:pubmed |
| pubmed-article:11580899 | pubmed:author | pubmed-author:PasqualeE BEB | lld:pubmed |
| pubmed-article:11580899 | pubmed:author | pubmed-author:IrieFF | lld:pubmed |
| pubmed-article:11580899 | pubmed:author | pubmed-author:KaloM SMS | lld:pubmed |
| pubmed-article:11580899 | pubmed:author | pubmed-author:EthellI MIM | lld:pubmed |
| pubmed-article:11580899 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:11580899 | pubmed:day | 27 | lld:pubmed |
| pubmed-article:11580899 | pubmed:volume | 31 | lld:pubmed |
| pubmed-article:11580899 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:11580899 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:11580899 | pubmed:pagination | 1001-13 | lld:pubmed |
| pubmed-article:11580899 | pubmed:dateRevised | 2009-11-19 | lld:pubmed |
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| pubmed-article:11580899 | pubmed:year | 2001 | lld:pubmed |
| pubmed-article:11580899 | pubmed:articleTitle | EphB/syndecan-2 signaling in dendritic spine morphogenesis. | lld:pubmed |
| pubmed-article:11580899 | pubmed:affiliation | The Burnham Institute, 10901 North Torrey Pines Road, La Jolla, CA 92037, USA. | lld:pubmed |
| pubmed-article:11580899 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:11580899 | pubmed:publicationType | Research Support, U.S. Gov't, P.H.S. | lld:pubmed |
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