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. 2016 Jun 30;7:262. doi: 10.3389/fimmu.2016.00262

Table 1.

Phenotype of circulating and tissue-resident CD56bright NK cells.

Reference Blood (13, 15, 17, 38) Lymph node, spleen, marrow (13, 18) Tonsil (18, 44) Liver (15, 45, 46) Uterus (16, 17, 20, 48, 49)
Definition CD69+
CXCR6+
NKp44+
CD103+
CD69+
CXCR6+
CD49a+
CD103
CD49a+
CD103+

CD56 ++ + +/++ + +++ +++
CD69 + + + +
Cytokine receptors
CD117 (c-kit) % N.A. N.A.
CD127 (IL7-Rα) % N.A.
Chemokine receptors
CCR7 +
CCR5 % N.A. %
CXCR6 + + + N.A. N.A.
NK cell receptors
DNAM1 + % % % a a
KIR % % %
NKp44 + %
NKp46 + ++ ++ ++ + +
Adhesion molecules
CD9 N.A. % N.A. % +
CD49a (ITGα1) + + +
CD62L (L-selectin) +
CD103 (ITGαE) + N.A. +
ITGβ7 N.A. N.A. + N.A. +

The cell surface markers which are discriminative for circulating CD56bright NK cells, lymph node-, spleen-, bone marrow-, tonsil-, liver-, and uterus-resident NK cells are summarized. Uterus-resident NK cells can be subdivided based on CD103 expression.

++ and +++ indicate relatively higher levels of expression.

% indicates that only a fraction of the NK cell population is positive for the marker.

aContradicting literature exist on the DNAM expression on uterine NK cells.

N.A., not assessed.