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Orr MT , Wu J , Fang M , Sigal LJ , Spee P , Egebjerg T , Dissen E , Fossum S , Phillips JH , Lanier LL
Development and Function of CD94-Deficient Natural Killer Cells
PLoS One. 2010 ;5(12) :e15184
PMID: 21151939 PMCID: PMC2997080 URL: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&dopt=Citation&list_uids=21151939
AbstractThe CD94 transmembrane-anchored glycoprotein forms disulfide-bonded heterodimers with the NKG2A subunit to form an inhibitory receptor or with the NKG2C or NKG2E subunits to assemble a receptor complex with activating DAP12 signaling proteins. CD94 receptors expressed on human and mouse NK cells and T cells have been proposed to be important in NK cell tolerance to self, play an important role in NK cell development, and contribute to NK cell-mediated immunity to certain infections including human cytomegalovirus. We generated a gene-targeted CD94-deficient mouse to understand the role of CD94 receptors in NK cell biology. CD94-deficient NK cells develop normally and efficiently kill NK cell-susceptible targets. Lack of these CD94 receptors does not alter control of mouse cytomegalovirus, lymphocytic choriomeningitis virus, vaccinia virus, or Listeria monocytogenes. Thus, the expression of CD94 and its associated NKG2A, NKG2C, and NKG2E subunits is dispensable for NK cell development, education, and many NK cell functions.
NotesOrr, Mark T Wu, Jun Fang, Min Sigal, Luis J Spee, Pieter Egebjerg, Thomas Dissen, Erik Fossum, Sigbjorn Phillips, Joseph H Lanier, Lewis L United States PloS one PLoS One. 2010 Dec 3;5(12):e15184.