Involvement of gangliosides in the process of Cbp/PAG phosphorylation by Lyn in developing cerebellar growth cones

The association of gangliosides with specific proteins in the central nervous system was examined by coimmunoprecipitation with an anti‐ganglioside antibody. The monoclonal antibody to the ganglioside GD3 (R24) immunoprecipitated the Csk (C‐terminal src kinase)‐binding protein (Cbp). Sucrose density...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of neurochemistry 2013-02, Vol.124 (4), p.514-522
Hauptverfasser: Sekino‐Suzuki, Naoko, Yuyama, Kohei, Miki, Toshiaki, Kaneda, Mizuho, Suzuki, Hidenori, Yamamoto, Naomasa, Yamamoto, Tadashi, Oneyama, Chitose, Okada, Masato, Kasahara, Kohji
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The association of gangliosides with specific proteins in the central nervous system was examined by coimmunoprecipitation with an anti‐ganglioside antibody. The monoclonal antibody to the ganglioside GD3 (R24) immunoprecipitated the Csk (C‐terminal src kinase)‐binding protein (Cbp). Sucrose density gradient analysis showed that Cbp of rat cerebellum was detected in detergent‐resistant membrane (DRM) raft fractions. R24 treatment of the rat primary cerebellar cultures induced Lyn activation and tyrosine phosphorylation of Cbp. Treatment with anti‐ganglioside GD1b antibody also induced tyrosine phosphorylation. Furthermore, over‐expressions of Lyn and Cbp in Chinese hamster ovary (CHO) cells resulted in tyrosine 314 phosphorylation of Cbp, which indicates that Cbp is a substrate for Lyn. Immunoblotting analysis showed that the active form of Lyn and the Tyr314‐phosphorylated form of Cbp were highly accumulated in the DRM raft fraction prepared from the developing cerebellum compared with the DRM raft fraction of the adult one. In addition, Lyn and the Tyr314‐phosphorylated Cbp were highly concentrated in the growth cone fraction prepared from the developing cerebellum. Immunoelectron microscopy showed that Cbp and GAP‐43, a growth cone marker, are localized in the same vesicles of the growth cone fraction. These results suggest that Cbp functionally associates with gangliosides on growth cone rafts in developing cerebella. Functional association of gangliosides with Csk‐binding protein in cerebellar growth cone rafts This work aimed to study the role of gangliosides in the nervous system. We demonstrated that anti‐ganglioside antibody co‐immunoprecipitated Csk‐binding protein (Cbp) and Src family kinase Lyn from cerebellum, and treatment of primary cerebellar cultures with anti‐ganglioside antibody induced Lyn activation and tyrosine 314 phosphorylation of Cbp in growth cone rafts. This suggests that gangliosides are platforms of transmembrane signaling by Lyn and Cbp. Read the Editorial Highlight for this article on doi: 10.1111/jnc.12134.
ISSN:0022-3042
1471-4159
DOI:10.1111/jnc.12040