Aberrant expressions of endometrial Id3 and CTLA-4 are associated with unexplained repeated implantation failure and recurrent miscarriage.
Jin-Li DingLiang-Hui DiaoTai-Lang YinChun-Yu HuangBiao YinCong ChenYi ZhangJie LiYan-Xiang ChengYong ZengJing YangPublished in: American journal of reproductive immunology (New York, N.Y. : 1989) (2017)
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® 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.
Keyphrases
- pulmonary tuberculosis
- induced apoptosis
- cell cycle arrest
- binding protein
- high resolution
- regulatory t cells
- endothelial cells
- deep learning
- mycobacterium tuberculosis
- cell death
- vascular endothelial growth factor
- pregnant women
- high throughput
- convolutional neural network
- mass spectrometry
- single cell
- wound healing
- circulating tumor