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  Deletion of a kinesin I motor unmasks a mechanism of homeostatic branching control by neurotrophin-3

Auer, T. O., Xiao, T., Bercier, V., Gebhardt, C., Duroure, K., Concordet, J.-P., et al. (2015). Deletion of a kinesin I motor unmasks a mechanism of homeostatic branching control by neurotrophin-3. eLife, 4: e05061. doi:10.7554/eLife.05061.

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 Urheber:
Auer, Thomas O., Autor
Xiao, Tong, Autor
Bercier, Valerie, Autor
Gebhardt, Christoph, Autor
Duroure, Karine, Autor
Concordet, Jean-Paul, Autor
Wyart, Claire, Autor
Suster, Maximiliano, Autor
Kawakami, Koichi, Autor
Wittbrodt, Joachim, Autor
Baier, Herwig1, Autor           
Del Bene, Filippo, Autor
Affiliations:
1Department: Genes-Circuits-Behavior / Baier, MPI of Neurobiology, Max Planck Society, ou_1128545              

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Schlagwörter: NEURAL ACTIVITY; AXONAL-TRANSPORT; RETINOTECTAL PROJECTION; NEURONAL-ACTIVITY; ZEBRAFISH RETINA; INTRACELLULAR-TRANSPORT; SUPERFAMILY PROTEIN; ORGANELLE TRANSPORT; MOLECULAR-CLONING; BEHAVIORAL SCREEN
 Zusammenfassung: Development and function of highly polarized cells such as neurons depend on microtubule-associated intracellular transport, but little is known about contributions of specific molecular motors to the establishment of synaptic connections. In this study, we investigated the function of the Kinesin I heavy chain Kif5aa during retinotectal circuit formation in zebrafish. Targeted disruption of Kif5aa does not affect retinal ganglion cell differentiation, and retinal axons reach their topographically correct targets in the tectum, albeit with a delay. In vivo dynamic imaging showed that anterograde transport of mitochondria is impaired, as is synaptic transmission. Strikingly, disruption of presynaptic activity elicits upregulation of Neurotrophin-3 (Ntf3) in postsynaptic tectal cells. This in turn promotes exuberant branching of retinal axons by signaling through the TrkC receptor (Ntrk3). Thus, our study has uncovered an activity-dependent, retrograde signaling pathway that homeostatically controls axonal branching.

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Sprache(n): eng - English
 Datum: 2015-06-15
 Publikationsstatus: Erschienen
 Seiten: 26
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: Expertenbegutachtung
 Identifikatoren: ISI: 000356230400001
DOI: 10.7554/eLife.05061
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Titel: eLife
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: Cambridge : eLife Sciences Publications
Seiten: - Band / Heft: 4 Artikelnummer: e05061 Start- / Endseite: - Identifikator: ISSN: 2050-084X
CoNE: https://pure.mpg.de/cone/journals/resource/2050-084X