|
|
||||||||
Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138
Invariant (Ii) chain loss causes defective class II export, B cell maturation, and reduced DM stability. In this study, we compare Ii chain and class II mutant mouse phenotypes to dissect these disturbances. The present results demonstrate that ER retention of 
complexes, and not
-chain aggregates, disrupts B cell development. In contrast, we fail to detect class II aggregates in Ii chain mutant thymi. Ii chain loss in NOD mice leads to defective class II export and formation of 
aggregates, but in this background, downstream signals are misregulated and mature B cells develop normally. Finally, Ii chain mutant strains all display reduced levels of DM, but mice expressing either p31 or p41 alone, and class II single chain mutants, are indistinguishable from wild type. We conclude that Ii chain contributions as a DM chaperone are independent of its role during class II export. This Ii chain/DM partnership favors class II peptide loading via conventional pathway(s).
This article has been cited by other articles:
![]() |
F. Vascotto, D. Lankar, G. Faure-Andre, P. Vargas, J. Diaz, D. Le Roux, M.-I. Yuseff, J.-B. Sibarita, M. Boes, G. Raposo, et al. The actin-based motor protein myosin II regulates MHC class II trafficking and BCR-driven antigen presentation J. Cell Biol., March 26, 2007; 176(7): 1007 - 1019. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. Neumann, A. Konig, and N. Koch Detection of aberrant association of DM with MHC class II subunits in the absence of invariant chain Int. Immunol., January 1, 2007; 19(1): 31 - 39. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. J. Mellanby, C. H. Koonce, A. Monti, J. M. Phillips, A. Cooke, and E. K. Bikoff Loss of Invariant Chain Protects Nonobese Diabetic Mice against Type 1 Diabetes J. Immunol., December 1, 2006; 177(11): 7588 - 7598. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |