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  The cytoplasmic domain of the ligand ephrinB2 is required for vascular morphogenesis but not cranial neural crest migration

Adams, R. H., Diella, F., Hennig, S., Helmbacher, F., Deutsch, U., & Klein, R. (2001). The cytoplasmic domain of the ligand ephrinB2 is required for vascular morphogenesis but not cranial neural crest migration. Cell, 104(1), 57-69. doi:10.1016/s0092-8674(01)00191-x.

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Genre: Zeitschriftenartikel

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 Urheber:
Adams, R. H., Autor
Diella, F., Autor
Hennig, Silvia, Autor
Helmbacher, F.1, Autor           
Deutsch, Urban, Autor
Klein, Rüdiger1, Autor           
Affiliations:
1European Molecular Biology Laboratory, Heidelberg, ou_persistent22              

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Schlagwörter: receptor tyrosine kinases eph receptors cardiovascular development sprouting angiogenesis commissural axons hindbrain gene angiopoietin-1 segmentation expression Biochemistry & Molecular Biology Cell Biology
 Zusammenfassung: The transmembrane ligand ephrinB2 and its cognate Eph receptor tyrosine kinases are important regulators of vascular morphogenesis. EphrinB2 may have an active signaling role, resulting in bi-directional signal transduction downstream of both ephrinB2 and Eph receptors. To separate the ligand and receptorlike functions of ephrinB2 in mice, we replaced the endogenous gene by cDNAs encoding either carboxyterminally truncated (ephrinB2(DeltaC)) or, as a control, full-length ligand (ephrinB2(WT)). While homozygous ephrinB2(WT/WT) animals were viable and fertile, loss of the ephrinB2 cytoplasmic domain resulted in midgestation lethality similar to ephrinB2 null mutants (ephrinB2(KO)). The truncated ligand was sufficient to restore guidance of migrating cranial neural crest cells, but ephrinB2(DeltaC/DeltaC) embryos showed defects in vasculogenesis and angiogenesis very similar to those observed in ephrinB2(KO/KO) animals. Our results indicate distinct requirements of functions mediated by the ephrinB carboxyterminus for developmental processes in the vertebrate embryo.

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Sprache(n): eng - English
 Datum: 2001
 Publikationsstatus: Erschienen
 Seiten: -
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: -
 Identifikatoren: Anderer: WOS:000166882300007
DOI: 10.1016/s0092-8674(01)00191-x
ISSN: 0092-8674
 Art des Abschluß: -

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Titel: Cell
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: Cambridge, Mass. : Cell Press
Seiten: - Band / Heft: 104 (1) Artikelnummer: - Start- / Endseite: 57 - 69 Identifikator: ISSN: 0092-8674
CoNE: https://pure.mpg.de/cone/journals/resource/954925463183