Human NKG2E Is Expressed and Forms an Intracytoplasmic Complex with CD94 and DAP12
Author(s) -
Gerasim A. Orbelyan,
Fangming Tang,
Benjamin Sally,
Jason Solus,
Bertrand Meresse,
Cezary Ciszewski,
JeanChristophe Grenier,
Luis B. Barreiro,
Lewis L. Lanier,
Bana Jabrì
Publication year - 2014
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.1400556
Subject(s) - intracellular , microbiology and biotechnology , endoplasmic reticulum , extracellular , receptor , biology , mhc class i , nkg2d , peptide sequence , major histocompatibility complex , biochemistry , gene , in vitro , cytotoxicity
The NKG2 family of NK receptors includes activating and inhibitory members. With the exception of the homodimer-forming NKG2D, NKG2 receptors recognize the nonclassical MHC class I molecule HLA-E, and they can be subdivided into two groups: those that associate with and signal through DAP12 to activate cells, and those that contain an ITIM motif to promote inhibition. The function of NKG2 family member NKG2E is unclear in humans, and its surface expression has never been conclusively established, largely because there is no Ab that binds specifically to NKG2E. Seeking to determine a role for this molecule, we chose to investigate its expression and ability to form complexes with intracellular signaling molecules. We found that NKG2E was capable of associating with CD94 and DAP12 but that the complex was retained intracellularly at the endoplasmic reticulum instead of being expressed on cell surfaces, and that this localization was dependent on a sequence of hydrophobic amino acids in the extracellular domain of NKG2E. Because this particular sequence has emerged and been conserved selectively among higher order primates evolutionarily, this observation raises the intriguing possibility that NKG2E may function as an intracellular protein.
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