Characterization of CD1e, a third type of CD1 molecule expressed in dendritic cells

被引:73
作者
Angénieux, C
Salamero, J
Fricker, D
Cazenave, JP
Goud, B
Hanau, D
de la Salle, H [1 ]
机构
[1] Etab Francais Sang Alsace, Equipe Propre INSERM 99 08, F-67065 Strasbourg, France
[2] Etab Francais Sang Alsace, Unite INSERM 311, F-67065 Strasbourg, France
[3] Inst Curie, UMR CNRS 144, F-75005 Paris, France
关键词
D O I
10.1074/jbc.M007082200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Dendritic cells express several alternatively spliced CD1e mRNAs. These molecules encode proteins characterized by the presence of either one, two, or three cu domains and either a 51- or 63-amino acid cytoplasmic domain. Moreover, mRNAs encoding isoforms lacking the transmembrane domain are observed. Several of these CD1e isoforms were expressed in transfected cells, and two of them, with three a domains, displayed a particular processing pathway. These latter isoforms slowly leave the endoplasmic reticulum due to the presence of atypical dilysine motifs in the cytoplasmic tail. These molecules are associated with the beta (2)-microglobulin and accumulate in late Golgi and late endosomal compartments. In the latter compartments, they are cleaved into soluble forms that appear to be stable, In dendritic cells, these isoforms are mainly located in the Golgi apparatus, and upon maturation they are redistributed to late endosomal compartments. This work demonstrates the existence of CD1e molecules. As compared with other CD1 molecules, CD1e displays fundamentally different properties and therefore may represent a third type of CD1 molecules.
引用
收藏
页码:37757 / 37764
页数:8
相关论文
共 27 条
[21]  
2-U
[22]   EEA1 links PI(3)K function to Rab5 regulation of endosome fusion [J].
Simonsen, A ;
Lippé, R ;
Christoforidis, S ;
Gaullier, JM ;
Brech, A ;
Callaghan, J ;
Toh, BH ;
Murphy, C ;
Zerial, M ;
Stenmark, H .
NATURE, 1998, 394 (6692) :494-498
[23]   Immunolocalization of CD1d in human intestinal epithelial cells and identification of a β2-microglobulin-associated form [J].
Somnay-Wadgaonkar, K ;
Nusrat, A ;
Kim, HS ;
Canchis, WP ;
Balk, SP ;
Colgan, SP ;
Blumberg, RS .
INTERNATIONAL IMMUNOLOGY, 1999, 11 (03) :383-392
[24]   CD1-reactive natural killer T cells are required for development of systemic tolerance through an immune-privileged site [J].
Sonoda, KH ;
Exley, M ;
Snapper, S ;
Balk, SP ;
Stein-Streilein, J .
JOURNAL OF EXPERIMENTAL MEDICINE, 1999, 190 (09) :1215-1225
[25]   Separate pathways for antigen presentation by CD1 molecules [J].
Sugita, M ;
Grant, EP ;
van Donselaar, E ;
Hsu, VW ;
Rogers, RA ;
Peters, PJ ;
Brenner, MB .
IMMUNITY, 1999, 11 (06) :743-752
[26]   Signal-mediated sorting of membrane proteins between the endoplasmic reticulum and the Golgi apparatus [J].
Teasdale, RD ;
Jackson, MR .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 1996, 12 :27-54
[27]   ALTERNATIVE SPLICING GENERATES SECRETORY ISOFORMS OF HUMAN CD1 [J].
WOOLFSON, A ;
MILSTEIN, C .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (14) :6683-6687