Nogo-A, -B, and -C are found on the cell surface and interact together in many different cell types.

Date publication

avril 2005

Auteurs

Membres identifiés du Cancéropôle Est :
Dr LOEFFLER Jean-Philippe

Tous les auteurs :
Dodd DA, Niederoest B, Bloechlinger S, Dupuis L, Loeffler JP, Schwab ME

Lien Pubmed

https://www.ncbi.nlm.nih.gov/pubmed/15640160

Résumé

Nogo-A, -B, and -C are generated from the Nogo/RTN-4 gene and share a highly conserved C-terminal domain. They lack an N-terminal signal sequence and are predominantly localized to the endoplasmic reticulum (ER). We found the N terminus of endogenous Nogo-A exposed on the surface of fibroblasts, DRG neurons, and myoblasts. Surface-expressed Nogo-A was also present on presynaptic terminals of the neuromuscular junction and on DRG neurons in vivo. Surface biotinylations confirmed the presence of all Nogo isoforms on the surface. To search for proteins that interact with Nogo-A and suggest a function for the large intracellular pool of Nogo-A, immunoprecipitations were performed. Surprisingly, the most predominant proteins that interact with Nogo-A are Nogo-B and Nogo-C as seen with radiolabeled lysates and as confirmed by Western blotting in multiple cell lines. Nogo-A, -B, and -C share a 180-amino acid C-terminal domain with two highly conserved hydrophobic stretches that could form a channel or transporter in the ER and/or on the cell surface.

Référence

J Biol Chem. 2005 Apr 1;280(13):12494-502