Dendritic cells express several alternatively spliced CD1e mRNAs. These mol
ecules encode proteins characterized by the presence of either one, two, or
three cu domains and either a 51- or 63-amino acid cytoplasmic domain. Mor
eover, mRNAs encoding isoforms lacking the transmembrane domain are observe
d. Several of these CD1e isoforms were expressed in transfected cells, and
two of them, with three a domains, displayed a particular processing pathwa
y. These latter isoforms slowly leave the endoplasmic reticulum due to the
presence of atypical dilysine motifs in the cytoplasmic tail. These molecul
es are associated with the beta (2)-microglobulin and accumulate in late Go
lgi and late endosomal compartments. In the latter compartments, they are c
leaved into soluble forms that appear to be stable, In dendritic cells, the
se isoforms are mainly located in the Golgi apparatus, and upon maturation
they are redistributed to late endosomal compartments. This work demonstrat
es the existence of CD1e molecules. As compared with other CD1 molecules, C
D1e displays fundamentally different properties and therefore may represent
a third type of CD1 molecules.