The Cytoplasmic Tail of Invariant Chain Regulates Endosome Fusion and Morphology (Articolo in rivista)

Type
Label
  • The Cytoplasmic Tail of Invariant Chain Regulates Endosome Fusion and Morphology (Articolo in rivista) (literal)
Anno
  • 2002-01-01T00:00:00+01:00 (literal)
Alternative label
  • Nordeng, T. W., Gregers, T. F., Kongsvik, T. L., Méresse, S., Gorvel, J.-P., Jourdan, F., MOTTA, A, and Bakke, O., (2002)
    The Cytoplasmic Tail of Invariant Chain Regulates Endosome Fusion and Morphology
    in Molecular biology of the cell
    (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
  • Nordeng, T. W., Gregers, T. F., Kongsvik, T. L., Méresse, S., Gorvel, J.-P., Jourdan, F., MOTTA, A, and Bakke, O., (literal)
Pagina inizio
  • 1846 (literal)
Pagina fine
  • 1856 (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#altreInformazioni
  • La comprensione di questi meccanismi consente di \"controllare\" l'efficacia della presentazione degli antigeni, riducendo potenzialmente il richio derivante dalle infezioni. (literal)
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  • 13 (literal)
Rivista
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  • Progetto finanziato dalla UE; F. Jourdan, post doc dell'ICB (literal)
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  • Studio multidisciplinare (finanziato dalla UE) dei meccanismi che regolano la fusione endosomica (cioè la formazione di vescicole) della proteina Invariant chain. Essa svolge funzioni importanti nella presentazione di antigeni esogeni al sistema di riconoscimento MHC. (literal)
Note
  • ISI Web of Science (WOS) (literal)
Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
  • T.W. NORDENG, T.F. GREGERS, T.L. KONKSVIK, O. BAKKE: UNI Oslo; S. MERESSE, J.-P. GORVEL: CNRS-INSERM, Marsiglia; F. JOURDAN, A. MOTTA: ICB, Pozzuoli (literal)
Titolo
  • The Cytoplasmic Tail of Invariant Chain Regulates Endosome Fusion and Morphology (literal)
Abstract
  • The major histocompatibility complex class II associated invariant chain (Ii) has been shown to inhibit endocytic transport and to increase the size of endosomes. We have recently found that this property has a significant impact on antigen processing and presentation. Here, we show in a cell-free endosome fusion assay that expression of Ii can increase fusion after phosphatidylinositol 3-kinase activity is blocked by wortmannin. In live cells wortmannin was also not able to block formation of the Ii-induced enlarged endosomes. The effects of Ii on endosomal transport and morphology depend on elements within the cytoplasmic tail. Data from mutagenesis analysis and nuclear magnetic resonance-based structure calculations of the Ii cytoplasmic tail demonstrate that free negative charges that are not involved in internal salt bridges are essential for both interactions between the tails and for the formation of enlarged endosomes. This correlation indicates that it is interactions between the Ii cytoplasmic tails that are involved in endosome fusion. The combined data from live cells, cell-free assays, and molecular dynamic simulations suggest that Ii molecules on different vesicles can promote endosome docking and fusion and thereby control endosomal traffic of membrane proteins and endosomal content. (literal)
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