A support for this hypothesis comes from a mouse in vivo model in which NK cells, which were chronically exposed to the
NKG2D ligand, were impaired in their NKG2D-dependent cytotoxicity, but constitutively produced IFN-γ.59 It is therefore possible that chronic stimulation of dNK-activating receptors by their ligands could be responsible for their lack of cytotoxicity toward fetal cells and their enhanced ability to produce growth factors. Soluble factors produced by neighboring decidual, immune or trophoblast cells can also influence dNK cells. These soluble factors could be cytokines, such as IL-1531 or other proteins, such as trophoblast-derived soluble HLA-G.60,61 Another possibility is hypoxic stress within the decidua that might influence the expression of the ligands for the dNK receptors. Indeed, MEK inhibitor tissue stress, such as genotoxic stress, was shown to up-regulate the expression of NKG2D-ligands selleck screening library that stimulate NK cells.62 Further study is needed to support this hypothesis. The mechanisms controlling the accumulation of CD56bright CD16− NK cells in the decidua are still being investigated. Several possibilities for the origin of dNK cells have been
proposed. One possibility is that NK cells are recruited from other organs or from the peripheral blood to the decidua, where they undergo further tissue specific differentiation. Alternatively, it was suggested that self Ergoloid renewal from local progenitor cells is the mechanism responsible for the accumulation of NK cells in the decidua, as will be discussed later. It is also possible that dNK cells originate in eNK cells that already
reside in the tissue and undergo further differentiation into dNK cells in the new environment that pregnancy creates. Our suggestion (as discuss below) is that dNK cells are probably a heterogeneous population that encompasses all of the above. Several studies support the notion that dNK cells originate in peripheral blood NK cells.43,63 Keskin et al.64 suggested that dNK cells might originate from the CD56dim CD16+ peripheral blood NK cells that migrate to the decidua and differentiate locally to dNK cells under the influence of tissue-derived TGF-β and other factors. However, other studies support the hypothesis that the CD56bright CD16− dNK cells originate rather in the CD56bright CD16− NK subset. The recruitment of NK cells from the blood to the decidua involves adhesion molecules. l-selectin is highly expressed on CD56bright CD16− NK cells, as opposed to CD56dim CD16+ NK cells, and was shown to be involved in the initial adhesion to lymph node high endothelial venules, therefore giving the CD56bright CD16− NK cells an advantage in extravasation to tissues.65 Interestingly, CSPG-2, the ligand of l-selectin, was shown to be highly expressed in the tissue, during the secretory phase of the menstrual cycle.
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