J Clin Invest. 2013 Oct;123(10):4264-72. doi: 10.1172/JCI68991. Epub 2013 Sep 16.
Reduced trophoblast invasion and vascular conversion in decidua are thought to be the primary defect of common pregnancy disorders including preeclampsia and fetal growth restriction. Genetic studies suggest these conditions are linked to combinations of polymorphic killer cell Ig-like receptor (KIR) genes expressed by maternal decidual NK cells (dNK) and HLA-C genes expressed by fetal trophoblast. Inhibitory KIR2DL1 and activating KIR2DS1 both bind HLA-C2, but confer increased risk or protection from pregnancy disorders, respectively. The mechanisms underlying these genetic associations with opposing outcomes are unknown. We show that KIR2DS1 is highly expressed in dNK, stimulating strong activation of KIR2DS1+ dNK. We used microarrays to identify additional responses triggered by binding of KIR2DS1 or KIR2DL1 to HLA-C2 and found different responses in dNK coexpressing KIR2DS1 with KIR2DL1 compared with dNK only expressing KIR2DL1. Activation of KIR2DS1+ dNK by HLA-C2 stimulated production of soluble products including GM-CSF, detected by intracellular FACS and ELISA. We demonstrated that GM-CSF enhanced migration of primary trophoblast and JEG-3 trophoblast cells in vitro. These findings provide a molecular mechanism explaining how recognition of HLA class I molecules on fetal trophoblast by an activating KIR on maternal dNK may be beneficial for placentation.
蜕膜中滋养细胞侵袭和血管转化减少被认为是包括子痫前期和胎儿生长受限在内的常见妊娠疾病的主要缺陷。遗传研究表明,这些情况与母体蜕膜自然杀伤细胞 (dNK) 表达的杀伤细胞免疫球蛋白样受体 (KIR) 基因和胎儿滋养细胞表达的 HLA-C 基因的多态组合有关。抑制性 KIR2DL1 和激活型 KIR2DS1 均可与 HLA-C2 结合,但分别增加或降低妊娠疾病的风险。这些遗传关联与相反结果相关的机制尚不清楚。我们表明 KIR2DS1 在 dNK 中高度表达,刺激 KIR2DS1+ dNK 的强烈激活。我们使用微阵列来鉴定由 KIR2DS1 或 KIR2DL1 与 HLA-C2 结合引发的其他反应,并发现与仅表达 KIR2DL1 的 dNK 相比,共表达 KIR2DS1 和 KIR2DL1 的 dNK 存在不同的反应。HLA-C2 刺激 KIR2DS1+ dNK 的激活会刺激包括 GM-CSF 在内的可溶性产物的产生,这可以通过细胞内 FACS 和 ELISA 检测到。我们证明 GM-CSF 增强了原发性滋养细胞和 JEG-3 滋养细胞在体外的迁移。这些发现提供了一个分子机制,解释了母体 dNK 上的激活型 KIR 对胎儿滋养细胞上 HLA Ⅰ类分子的识别如何有益于胎盘形成。