Increased expression of angiogenic cytokines in CD56+ uterine natural killer cells from women with recurrent miscarriage

反复流产 子宫内膜 血管生成 血管生长素 细胞因子 男科 流产 生物 医学 内分泌学 内科学 怀孕 遗传学
作者
Xiaoyan Chen,Yingyu Liu,Wing Ching Cheung,Yiwei Zhao,Jin Huang,Jacqueline Pui Wah Chung,Chi Chiu Wang,Tin‐Chiu Li
出处
期刊:Cytokine [Elsevier BV]
卷期号:110: 272-276 被引量:18
标识
DOI:10.1016/j.cyto.2018.01.013
摘要

To compare the expression pattern of angiogenic cytokines in CD56+ uNK cells from peri-implantation endometrium in women with a history of recurrent miscarriage and fertile controls.28 women were recruited, from which 18 women were diagnosed as recurrent miscarriage and 10 women were of proven fertility. Endometrial biopsy samples were obtained precisely 7 days after luteinization hormone surge in a natural cycle. The angiogenic profile of isolated CD56+ uNK cells was determined by RayBio human angiogenesis antibody array G Series 1000. Differentially expressed angiogenic cytokines between groups were validated by ELISA kits.CD56+ uNK cells freshly isolated from peri-implantation endometrium were determined to be >90% pure. Angiogenic cytokine array demonstrated that CD56+ uNK cells are one of the angiogenic factors producers in endometrium around the time of embryo implantation. A differential angiogenic cytokine expression profile was found between two groups, with significantly higher expressions of angiogenin, VEGF-A and bFGF in CD56+ uNK cells from women with recurrent miscarriage, compared with fertile controls.Differential angiogenic cytokine profile of isolated CD56+ uNK cells suggested the role of uNK cells in the altered endometrial vascularity at the time of implantation, which may account for the endometrial contribution to recurrent miscarriage.

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