To Investigate How Secreted-embryo-derived Trypsin Initiates, Maintains and Terminates Ca2+ (Intracellular Calcium) Signals in Uterine Epithelial Cells
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 81
- 试验地点
- 1
- 主要终点
- Change in markers of protein
研究概览
简要总结
To develop a deeper understanding of endometrial-embryo crosstalk through basic research, uncover therapeutic targets and to improve reproductive outcome.
详细描述
Pregnancy is a complex and highly coordinated physiological process that involves implantation of a hatched blastocyst into a decidualizing endometrium. The main purpose of implantation is to ensure that the blastocyst firmly anchors into the decidual stroma, which allows further development by enabling placentation. Although a multitude of cellular events and molecular pathways involved in embryo-uterine crosstalk have been identified in mouse models, a comprehensive understanding of human embryo-uterine interaction is still missing. Our work indicates that endometrial epithelial Ca2+ signalling in response to serine proteases released by human embryos plays an important role in maternal recognition and selection of the conceptus at implantation. Previous studies have demonstrated that trophoblast spheroids can elevate [Ca2+]i in human uterine epithelial cell line (Ishikawa) by activating Ca2+ entry via mechano-sensitive Ca2+ permeable channels leading to the induction of epithelial adhesiveness. However, the mechanism(s) mediating the protease-induced [Ca2+]i transients in human uterine epithelium have not been studied to date. Investigators hypothesise that Na+ entry into the intravillous space via trypsin-activated ENaC will depolarise the cellular membrane and increase [Na+]v sufficiently high to reverse the sodium/calcium exchanger providing means for Ca2+ entry into the intravillous space. Ca2+ diffusion from the microvilli into the bulk cytoplasm will increase [Ca2+]i and, in parallel with SOCE, act as a source for re-filling of the ER. Increased [Ca2+]i will also activate the BK channels leading to repolarisation and termination of Ca2+ entry via the NCX.
By using spent medium from embryos, which will undergo pre-implantation genetic testing, it will become possible to determine, whether the above mentioned mechanisms are influenced by the ploidy status of the embryo.
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 36 Years(Adult)
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Couples with primary / secondary infertility who are planned to undergo ICSI treatment with PGT-A
- •Age of each partner above 18 years
排除标准
- •Couples with consanguinity (couple who is 1st or 2nd degree cousins)
- •Couples in whom the female partner has a history of:
- •Chemotherapy or radiation which impacts the ovarian reserve
- •Surgery at the ovaries / adnex region
- •Endometriosis
- •Couples in whom the male partner has a history of:
- •Chemotherapy / Radiation which impacts the semen result
- •Surgery at the testicles
- •Vasectomy
- •Surgery for reversal of vasectomy
- •Semen obtained by fine needle aspiration (FNA) or Testicular sperm extraction (TESE)
结局指标
主要结局
Change in markers of protein
时间窗: 1 day
Change in markers of protein (PAR2, (p) and SGK1, NFkB, ORAI1-3 and STIM1-2 and COX2) using Western blotting
Change in peak and slope levels of intracellular calcium
时间窗: 1 day
Change in peak and slope levels of intracellular calcium
Change in morphohology of cells after incubation with embryo media
时间窗: 1 day
Change in morphohology of cells after incubation with embryo media
次要结局
- Embryo quality on day 3(1 day)
- Embryo quality on day 5 (Gardner and Schoolcraft,1999)(1 day)
- Performance of ICSI(1 day)
研究者
Barbara Lawrenz
Scientific Director
ART Fertility Clinics LLC
