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The Nogo-66 Receptors NgR1 and NgR3 Are Required for Commissural Axon Pathfinding

Vaccaro, Giuseppe; Dumoulin, Alexandre; Zuñiga, Nikole R; Bandtlow, Christine E; Stoeckli, Esther T (2022). The Nogo-66 Receptors NgR1 and NgR3 Are Required for Commissural Axon Pathfinding. Journal of Neuroscience, 42(20):4087-4100.

Abstract

Nogo-66 receptors (NgR1-3) are glycosylphosphatidyl inositol-linked proteins that belong to the leucine-rich repeat superfamily. Through binding to myelin-associated inhibitors, NgRs contribute to the inhibition of axonal regeneration after spinal cord injury. Their role in limiting synaptic plasticity and axonal outgrowth in the adult CNS has been described previously, but not much is known about their role during the development of the nervous system. Here, we show that NgR1 and NgR3 mRNAs are expressed during spinal cord development of the chicken embryo. In particular, they are expressed in the dI1 subpopulation of commissural neurons during the time when their axons navigate toward and across the floorplate, the ventral midline of the spinal cord. To assess a potential role of NgR1 and NgR3 in axon guidance, we downregulated them using in ovo RNAi and analyzed the trajectory of commissural axons by tracing them in open-book preparations of spinal cords. Our results show that loss of either NgR1 or NgR3 causes axons to stall in the midline area and to interfere with the rostral turn of postcrossing axons. In addition, we also show that NgR1, but not NgR3, requires neuronal PlexinA2 for the regulation of commissural axon guidance.

Additional indexing

Item Type:Journal Article, refereed, original work
Communities & Collections:07 Faculty of Science > Institute of Molecular Life Sciences
Dewey Decimal Classification:570 Life sciences; biology
Uncontrolled Keywords:General Neuroscience
Language:English
Date:18 May 2022
Deposited On:29 Jun 2022 08:52
Last Modified:28 Aug 2024 01:35
Publisher:Society for Neuroscience
ISSN:0270-6474
Additional Information:Cover Article
OA Status:Hybrid
Free access at:PubMed ID. An embargo period may apply.
Publisher DOI:https://doi.org/10.1523/jneurosci.1390-21.2022
PubMed ID:35437280
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  • Licence: Creative Commons: Attribution 4.0 International (CC BY 4.0)

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