Natural killer (NK) cells express families of homologous receptors, members
of which either activate or inhibit NK cells. We demonstrate that mouse Ly
-49D is an activating receptor for the MI-IC antigen H2-D-d, which is also
a ligand for the related inhibitory receptor Ly-49A. To compare and contras
t their interactions with class I MHC ligand, we studied each of these rece
ptors expressed in a rat NK-cell line, RNK-16, for their capacity to recogn
ize wild-type or mutated H2-D-d. Our studies with Ly-49A reveal that functi
onal interaction with H2-D-d depends on residues in the floor of the H2-D-d
peptide-binding groove. The recent co-crystal of Ly-49A with H2-D-d indica
tes that these are not contact residues, thus they may contribute to alleli
c specificity through conformational changes in H2-D-d. We found that struc
tural requirements for functional recognition of H2-D-d by Ly-49D differ ma
rkedly from those for recognition by Ly-49A. We note that H2-D-d expression
on certain target cells is not sufficient to activate lysis mediated by Ly
-49D, though the additional requirements for functional interaction are not
yet identified. Here we review recent studies of Ly-49 receptor ligand spe
cificities and their molecular basis. The functions of these related recept
ors with opposing functions and shared allospecificity remains unclear.