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  Slit1a inhibits retinal ganglion cell arborization and synaptogenesis via Robo2-dependent and -independent pathways

Campbell, D. S., Stringham, S. A., Timm, A., Xiao, T., Law, M. Y., Baier, H., et al. (2007). Slit1a inhibits retinal ganglion cell arborization and synaptogenesis via Robo2-dependent and -independent pathways. Neuron, 55(2), 231-245. doi:10.1016/j.neuron.2007.06.034.

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 Urheber:
Campbell, D. S., Autor
Stringham, S. A., Autor
Timm, A., Autor
Xiao, T., Autor
Law, M. Y., Autor
Baier, Herwig1, Autor           
Nonet, M. L., Autor
Chien, C. B., Autor
Affiliations:
1University of California, San Francisco, U.S.A., ou_persistent22              

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Schlagwörter: repulsive axon guidance in-vivo retinotectal projection synapse formation embryonic zebrafish roundabout expression receptor system growth Neurosciences & Neurology
 Zusammenfassung: Upon arriving at their targets, developing axons cease pathfinding and begin instead to arborize and form synapses. To test whether CNS arborization and synaptogenesis are controlled by Slit-Robo signaling, we followed single retinal ganglion cell (RGC) arbors over time. ast (robo2) mutant and slit1a morphant arbors had more branch tips and greater arbor area and complexity compared to wild-type and concomitantly more presumptive presynaptic sites labeled with YFP-Rab3. Increased arborization in ast was phenocopied by dominant-negative Robo2 expressed in single RGCs and rescued by full-length Robo2, indicating that Robo2 acts cell-autonomously. Time-lapse imaging revealed that ast and slit1a morphant arbors stabilized earlier than wild-type, suggesting a role for Slit-Robo signaling in preventing arbor maturation. Genetic analysis showed that Slit1a acts both through Robo2 and Robo2-independent mechanisms. Unlike previous PNS studies showing that Slits promote branching, our results show that Slits inhibit arborization and synaptogenesis in the CNS.

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Sprache(n): eng - English
 Datum: 2007
 Publikationsstatus: Erschienen
 Seiten: -
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: -
 Identifikatoren: Anderer: WOS:000248635800008
DOI: 10.1016/j.neuron.2007.06.034
ISSN: 0896-6273
 Art des Abschluß: -

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Titel: Neuron
Genre der Quelle: Zeitschrift
 Urheber:
Affiliations:
Ort, Verlag, Ausgabe: Cambridge, Mass. : Cell Press
Seiten: - Band / Heft: 55 (2) Artikelnummer: - Start- / Endseite: 231 - 245 Identifikator: ISSN: 0896-6273
CoNE: https://pure.mpg.de/cone/journals/resource/954925560565