TY - JOUR
T1 - Cutting edge
T2 - FcR-like 6 is an MHC class II receptor
AU - Schreeder, Daniel M.
AU - Cannon, John P.
AU - Wu, Jiongru
AU - Li, Ran
AU - Shakhmatov, Mikhail A.
AU - Davis, Randall S.
PY - 2010/7/1
Y1 - 2010/7/1
N2 - Receptors for the Fc portion of Ig have been extensively characterized and are known to regulate humoral responses, but members of the closely related FcR-like (FCRL) family have not been found to bind Ig, and to date, no ligand has been identified for any FCRL. Using a cell-based GFP reporter system and a recombinant Fc chimeric protein, we show that human FCRL6, a receptor selectively expressed by cytotoxic T and NK cells, directly binds HLA-DR, an MHC class II molecule. Given the similarity among constant regions of Ig and MHC molecules, these findings suggest that representatives of the FcR and FCRL multigene families may have independently evolved to engage two ancestral elements fundamental to adaptive immunity. This discovery may offer new insight into the interaction between cytotoxic lymphocytes and APCs and may have important implications for better understanding HLA disease susceptibility and pathogenesis.
AB - Receptors for the Fc portion of Ig have been extensively characterized and are known to regulate humoral responses, but members of the closely related FcR-like (FCRL) family have not been found to bind Ig, and to date, no ligand has been identified for any FCRL. Using a cell-based GFP reporter system and a recombinant Fc chimeric protein, we show that human FCRL6, a receptor selectively expressed by cytotoxic T and NK cells, directly binds HLA-DR, an MHC class II molecule. Given the similarity among constant regions of Ig and MHC molecules, these findings suggest that representatives of the FcR and FCRL multigene families may have independently evolved to engage two ancestral elements fundamental to adaptive immunity. This discovery may offer new insight into the interaction between cytotoxic lymphocytes and APCs and may have important implications for better understanding HLA disease susceptibility and pathogenesis.
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U2 - 10.4049/jimmunol.1000832
DO - 10.4049/jimmunol.1000832
M3 - Article
C2 - 20519654
AN - SCOPUS:77956215853
SN - 0022-1767
VL - 185
SP - 23
EP - 27
JO - Journal of Immunology
JF - Journal of Immunology
IS - 1
ER -