Aberrant expressions of endometrial Id3 and CTLA-4 are associated with unexplained repeated implantation failure and recurrent miscarriage

被引:23
作者
Ding, Jin-Li [1 ]
Diao, Liang-Hui [2 ]
Yin, Tai-Lang [1 ]
Huang, Chun-Yu [2 ]
Yin, Biao [2 ]
Chen, Cong [2 ]
Zhang, Yi [1 ]
Li, Jie [1 ]
Cheng, Yan-Xiang [1 ]
Zeng, Yong [2 ]
Yang, Jing [1 ]
机构
[1] Wuhan Univ, Reprod Med Ctr, Renmin Hosp, Wuhan, Peoples R China
[2] Shenzhen Zhongshan Urol Hosp, Shenzhen Key Lab Reprod Immunol Peri Implantat, Fertil Ctr, Shenzhen Zhongshan Inst Reprod & Genet, Shenzhen, Peoples R China
基金
中国国家自然科学基金;
关键词
CD34; cytotoxic T-lymphocyte-associated protein 4 (CTLA-4); forkhead box P3 (FOXP3); inhibitor of DNA-binding protein 3 (Id3); recurrent miscarriage (RM); repeated implantation failure (RIF); REGULATORY T-CELLS; MATERNAL-FETAL INTERFACE; MENSTRUAL-CYCLE; PREGNANCY LOSS; WOMEN; VASCULARIZATION; DIFFERENTIATION; ANGIOGENESIS; INHIBITOR; PROTEINS;
D O I
10.1111/aji.12632
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Inhibitor of DNA-binding protein 3 (Id3) is required for tumor angiogenesis and regulatory T-cell generation. However, the involvement of Id3 in unexplained repeated implantation failure (RIF) and recurrent miscarriage (RM) remains poorly understood. Immunohistochemistry was used to identify Id3, CD34, CTLA-4, and FOXP3 in the endometrium taken from the women with RIF (n=16), RM (n=16) and matched controls (n=8). The images were acquired and analyzed by the Vectra((R)) automated quantitative pathology imaging system. Percentage of Id3(+) cells was significantly higher in the endometrium of women with RIF and RM compared with controls. The numbers of Id3(+) and CD34(+) vessels in the endometrium were positively correlated in control but not in RIF or RM. Percentages of CTLA-4(+) cells, but not FOXP3(+) cells, were significantly increased in the endometrium of RIF and RM women than those in controls. We found aberrant expressions of endometrial Id3 and CTLA-4 in peri-implantation endometrium of women with RIF and RM, suggesting the negative roles of these angiogenesis and immune tolerance markers involving in regulating endometrium receptivity.
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页数:7
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