Format

Send to

Choose Destination
See comment in PubMed Commons below
J Immunol. 2014 Jul 15;193(2):610-6. doi: 10.4049/jimmunol.1400556. Epub 2014 Jun 16.

Human NKG2E is expressed and forms an intracytoplasmic complex with CD94 and DAP12.

Author information

1
Department of Medicine, University of Chicago, Chicago, IL 60637;
2
Sainte-Justine Hospital Research Centre, Montreal, Quebec H3T 1C5, Canada; Department of Pediatrics, University of Montreal, Montreal, Quebec H3T 1C5, Canada; and.
3
Department of Microbiology and Immunology, University of California San Francisco, San Francisco, CA 94143.
4
Department of Medicine, University of Chicago, Chicago, IL 60637; bjabri@medicine.bsd.uchicago.edu.

Abstract

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.

PMID:
24935923
PMCID:
PMC4091631
DOI:
10.4049/jimmunol.1400556
[Indexed for MEDLINE]
Free PMC Article
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Full text links

    Icon for HighWire Icon for PubMed Central
    Loading ...
    Support Center