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Possible Roles of KIR2DL4 Expression on uNK Cells in Human Pregnancy

Problem To investigate possible roles of the natural killer (NK) cell receptor killer immunoglobulin‐like receptor (KIR)2DL4 expressed on uterine NK (uNK) cells during pregnancy, we investigated KIR2DL4 expression on uNK cells isolated from patients with early recurrent spontaneous abortion (RSA) an...

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Published in:American journal of reproductive immunology (1989) 2007-04, Vol.57 (4), p.233-242
Main Authors: Yan, Wei-hua, Lin, Aifen, Chen, Bao-guo, Zhou, Mei-ying, Dai, Mei-zhen, Chen, Xue-jiao, Gan, Ling-hong, Zhu, Min, Shi, Wei-wu, Li, Bo-li
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Language:English
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Summary:Problem To investigate possible roles of the natural killer (NK) cell receptor killer immunoglobulin‐like receptor (KIR)2DL4 expressed on uterine NK (uNK) cells during pregnancy, we investigated KIR2DL4 expression on uNK cells isolated from patients with early recurrent spontaneous abortion (RSA) and normal early pregnancy women, and functions of KIR2DL4 was analyzed in vitro. Methods of the study Semi‐quantitative RT‐PCR analysis was introduced to detect KIR2DL4 messenger RNA (mRNA) expression on uNK cells. Cytotoxicity and cytokine production as the result of interaction of KIR2DL4 and its ligand human leukocyte antigen (HLA)‐G were analyzed in vitro with lactic dehydrogenase releasing method and enzyme‐linked immunosorbent assay, respectively. Results No significant difference in KIR2DL4 mRNA expression was observed, while the KIR2DL4 protein level in isolated uNK cells is much higher in normal controls than that in RSA patients. Data showed that HLA‐G transfection could not reverse the lysis of uNK against HLA‐G transfected K562 cells but induced cytokine production. Furthermore, we demonstrated that, via KIR2DL4, membrane‐bound HLA‐G could induce high cytotoxicity and cytokine production in a high cytotoxic, IL‐2 dependent human NK cell line NK‐92 cells. Conclusion Our data suggest that KIR2DL4 might play a crucial implication for human pregnancy.
ISSN:1046-7408
1600-0897
DOI:10.1111/j.1600-0897.2007.00469.x