Besides IFN-γ, mouse dNK cells also secrete colony stimulating factor-1 (CSF-1), IL-1, leukemia inhibitory factor (LIF),55 TNF-α, and VEGF.56 Studies of human dNK cells have shown

that dNK cells produce a variety of cytokines MI-503 solubility dmso and growth factors. At the mRNA level, it was shown that human dNK cells produce transcripts of GM-CSF, CSF-1, TNF-α, LIF, and IFN-γ.57 A recent study has shown that the engagement of NKp30, but not NKp46, induces the secretion of TNF-α, MIP1-α, MIP1-β, GM-CSF, and IFN-γ by human dNK cells that were shortly activated with IL-2 or IL-15 for 48 hr.45 Human dNK cells can also secrete IL-8 and IP-10 and it was demonstrated that these chemokines bind to their receptors on invasive trophoblasts causing trophoblast migration.43 Human dNK cells can also produce a variety of angiogenic factors, including several members of the VEGF family, PLGF, angiopoetin-2 (Ang-2), and NKG5.43 These findings further support the function of dNK cells as major regulators

Staurosporine of vascular remodeling during the early stage of pregnancy. The ability of dNK cells to secrete a variety of cytokines that support these developmental processes during pregnancy suggests that dNK cells must be activated in the tissue, rather than inhibited, to exert their constructive roles at the fetal-maternal interface and establish a normal pregnancy. Indeed, it has been shown that dNK clones expressing the activating receptor KIR2DS4 generated higher amounts of IL-8, IP-10, VEGF, and PLGF than clones expressing inhibitory receptors, such as KIR2DL1. This suggests that activation of dNK cells reduces the risk of pre-eclampsia, through the production of sufficient amounts of

growth factors and chemokines by dNK cells.43 These factors contribute to trophoblast invasion and vascular modifications, as discussed above. The study of Moffet’s group strongly supports this notion as well. Their study suggested that strong inhibition of dNK cells, as a result of interactions between certain KIR alleles on dNK cells and certain HLA-C allels on extravillous trophoblasts, increases the likelihood of pre-eclampsia. Furthermore, interactions Urocanase between KIRs and HLA-C, which induce activation of dNK cells, result in a better trophoblast invasion.58 The unique properties of dNK cells probably result from intense communication between these cells and their neighboring decidual cells, local cytokines, other immune cells, and secreted hormones that create the special microenvironment of this tissue. dNK cells are in close contact with invasive trophoblasts and local decidual cells49 and therefore, there is probably a constant exposure of dNK receptors to their ligands. Indeed, decidual stromal cells express unknown ligands for the dNK-activating receptors NKp30 and NKp44.43 In addition, purified HLA-G+ trophoblasts express unknown ligands for NKp44.

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