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Two Human ULBP/RAET1 Molecules with Transmembrane Regions Are Ligands for NKG2D
Author(s) -
Louise Bacon,
Robert A. Eagle,
Martina Meyer,
Nicholas Easom,
Neil T. Young,
John Trowsdale
Publication year - 2004
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.173.2.1078
Subject(s) - nkg2d , transmembrane protein , transmembrane domain , microbiology and biotechnology , chemistry , biology , biochemistry , receptor , cytotoxicity , in vitro
We characterized two novel members of the RAET1/ULBP gene cluster, RAET1E and RAET1G. The encoded proteins were similar to the ULBP in their class I-like alpha1 and alpha2 domains, but differed in that, instead of being GPI-anchored, their sequences were type 1 membrane-spanning molecules. Both proteins were capable of being expressed at the cell surface. Both proteins bound the activating receptor NKG2D, and RAET1G bound the human CMV protein UL16. The expression of diverse NKG2D-binding molecules in different tissues and with different properties is consistent with multiple modes of infection- or stress-induced activation.

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