Modulation of proteasomal activity required for the generation of a cytotoxic T lymphocyte-defined peptide derived from the tumor antigen MAGE-3.

Détails

Ressource 1Télécharger: BIB_9C9B3174B1D8.P001.pdf (193.45 [Ko])
Etat: Public
Version: de l'auteur
ID Serval
serval:BIB_9C9B3174B1D8
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Modulation of proteasomal activity required for the generation of a cytotoxic T lymphocyte-defined peptide derived from the tumor antigen MAGE-3.
Périodique
Journal of Experimental Medicine
Auteur(s)
Valmori D., Gileadi U., Servis C., Dunbar P.R., Cerottini J.C., Romero P., Cerundolo V., Lévy F.
ISSN
0022-1007[print], 0022-1007[linking]
Statut éditorial
Publié
Date de publication
1999
Volume
189
Numéro
6
Pages
895-906
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Résumé
We have analyzed the presentation of human histocompatability leukocyte antigen-A*0201-associated tumor peptide antigen MAGE-3271-279 by melanoma cells. We show that specific cytotoxic T lymphocyte (CTL)-recognizing cells transfected with a minigene encoding the preprocessed fragment MAGE-3271-279 failed to recognize cells expressing the full length MAGE-3 protein. Digestion of synthetic peptides extended at the NH2 or COOH terminus of MAGE-3271-279 with purified human proteasome revealed that the generation of the COOH terminus of the antigenic peptide was impaired. Surprisingly, addition of lactacystin to purified proteasome, though partially inhibitory, resulted in the generation of the antigenic peptide. Furthermore, treatment of melanoma cells expressing the MAGE-3 protein with lactacystin resulted in efficient lysis by MAGE-3271-279-specific CTL. We therefore postulate that the generation of antigenic peptides by the proteasome in cells can be modulated by the selective inhibition of certain of its enzymaticactivities.
Mots-clé
Acetylcysteine/analogs &amp, derivatives, Acetylcysteine/pharmacology, Antigen Presentation, Antigens, Neoplasm, Cysteine Endopeptidases/physiology, Humans, Multienzyme Complexes/physiology, Neoplasm Proteins/metabolism, Peptide Fragments/metabolism, Proteasome Endopeptidase Complex, T-Lymphocytes, Cytotoxic/immunology, Tumor Cells, Cultured
Pubmed
Web of science
Open Access
Oui
Création de la notice
28/01/2008 11:17
Dernière modification de la notice
20/08/2019 15:03
Données d'usage