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Human NKG2E Is Expressed and Forms an Intracytoplasmic Complex with CD94 and DAP12

Authors :
Jean-Christophe Grenier
Cezary Ciszewski
Luis B. Barreiro
Fangming Tang
Gerasim A. Orbelyan
Jason Solus
Bana Jabri
Lewis L. Lanier
Bertrand Meresse
Benjamin Sally
Source :
Journal of immunology (Baltimore, Md. : 1950), vol 193, iss 2, Orbelyan, GA; Tang, F; Sally, B; Solus, J; Meresse, B; Ciszewski, C; et al.(2014). Human NKG2E is expressed and forms an intracytoplasmic complex with CD94 and DAP12. Journal of Immunology, 193(2), 610-616. doi: 10.4049/jimmunol.1400556. UCSF: Retrieved from: http://www.escholarship.org/uc/item/3w53201r
Publication Year :
2014
Publisher :
The American Association of Immunologists, 2014.

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. Copyright © 2014 by The American Association of Immunologists, Inc.

Details

ISSN :
15506606 and 00221767
Volume :
193
Database :
OpenAIRE
Journal :
The Journal of Immunology
Accession number :
edsair.doi.dedup.....24249c2becd230d9c003225792868fe0
Full Text :
https://doi.org/10.4049/jimmunol.1400556