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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao The Journal of Compa...arrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
The Journal of Comparative Neurology
Article . 2012 . Peer-reviewed
License: Wiley Online Library User Agreement
Data sources: Crossref
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Migration of sympathetic preganglionic neurons in the spinal cord of a C3G‐deficient mouse suggests that C3G acts in the reelin signaling pathway

Authors: Yee Ping, Yip; Tim, Thomas; Anne K, Voss; Joseph W, Yip;

Migration of sympathetic preganglionic neurons in the spinal cord of a C3G‐deficient mouse suggests that C3G acts in the reelin signaling pathway

Abstract

AbstractProper positioning of sympathetic preganglionic neurons (SPNs) in the spinal cord is regulated by reelin signaling. SPNs in reeler (which lacks reelin), and in mice deficient in components of the reelin signaling pathway (reelin receptors VldlR and ApoER2, the cytoplasmic adaptor protein Dab1, Src and Fyn of the Src‐family of non‐receptor protein tyrosine kinases, and CrkL) are located adjacent to the central canal instead of in the intermediolateral column (IML) of the spinal cord. Events downstream of CrkL in control of SPN migration are unclear. The present study asks whether Rap guanine nucleotide exchange factor (GEF) 1 (C3G/Rapgef1), a Ras family GEF that binds CrkL, could act downstream in the reelin signaling pathway in control of SPN migration. SPN migration was examined in a hypopmorphic C3G mutant mouse (C3Ggt/gt) by using retrograde DiI labeling and NOS immunostaining. The results showed that SPN in the C3Ggt/gt mutant migrate abnormally toward the central canal as in reeler. However, unlike reeler, levels of reelin in the C3Ggt/gt spinal cord are normal, and Dab1 immunostaining is undetectable. These results provide genetic evidence that C3G regulates SPN migration, and suggest that C3G acts downstream in the reelin signaling pathway in control of SPN migration. J. Comp. Neurol., 520:3194–3202, 2012. © 2012 Wiley Periodicals, Inc.

Keywords

Neurons, Extracellular Matrix Proteins, Sympathetic Nervous System, Autonomic Fibers, Preganglionic, Cell Adhesion Molecules, Neuronal, Serine Endopeptidases, Nerve Tissue Proteins, Mice, Mice, Neurologic Mutants, Reelin Protein, Spinal Cord, Cell Movement, Mutation, Contactin 2, Animals, Guanine Nucleotide-Releasing Factor 2, Signal Transduction

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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
8
Average
Average
Average