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

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Free keywords: NEURAL ACTIVITY; AXONAL-TRANSPORT; RETINOTECTAL PROJECTION; NEURONAL-ACTIVITY; ZEBRAFISH RETINA; INTRACELLULAR-TRANSPORT; SUPERFAMILY PROTEIN; ORGANELLE TRANSPORT; MOLECULAR-CLONING; BEHAVIORAL SCREEN
 Abstract: 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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Language(s): eng - English
 Dates: 2015-06-15
 Publication Status: Issued
 Pages: 26
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: ISI: 000356230400001
DOI: 10.7554/eLife.05061
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Title: eLife
Source Genre: Journal
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Publ. Info: Cambridge : eLife Sciences Publications
Pages: - Volume / Issue: 4 Sequence Number: e05061 Start / End Page: - Identifier: ISSN: 2050-084X
CoNE: https://pure.mpg.de/cone/journals/resource/2050-084X