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Department of Molecular Biology, Princeton University, Princeton, NJ 08544
Mouse CD1.1 is an MHC class I-like, non-MHC-encoded, surface
glycoprotein that can be recognized by T cells, in particular
NK1.1+ T cells, a subset of
ß T cells with
semiinvariant TCRs that promptly releases potent cytokines such as IL-4
and IFN-
upon stimulation. To gain insight into the function of
CD1.1, a panel of nine mAbs was generated and used to biochemically
characterize and monitor the surface expression of CD1.1 on different
cell types. CD1.1 is a heavily glycosylated,
ß2-microglobulin-associated surface protein. Its
recognition by a panel of 12 V
14-positive and -negative CD1-specific
ß T cell hybridomas was blocked by two groups of mAbs that bound
to adjacent clusters of epitopes, indicating that different
ß TCRs
bind to the same region of CD1.1, presumably above the groove.
Remarkably, CD1.1 was mainly expressed by dendritic cells, B cells, and
macrophages, suggesting a function in Ag presentation to Th cells.
Furthermore, the cell type that expressed the highest levels of CD1.1
was the splenic marginal zone B cell, a distinct subset of B cells that
also expresses CD21 (the C3d receptor) and may be involved in natural
responses to bacterial Ags. Altogether, the results support the idea
that CD1.1 may function in recruiting a form of innate help from
specialized cytokine producer
ß T cells to APCs, a role that might
be important at the preadaptive phase of immune responses to some
microbial pathogens.
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