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临床试验/NCT04865367
NCT04865367已完成不适用

To Investigate How Secreted-embryo-derived Trypsin Initiates, Maintains and Terminates Ca2+ (Intracellular Calcium) Signals in Uterine Epithelial Cells

ART Fertility Clinics LLC1 个研究点 分布在 1 个国家目标入组 81 人开始时间: 2021年11月4日最近更新:
适应症

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

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

申办方类型
Other
责任方
Principal Investigator
主要研究者

Barbara Lawrenz

Scientific Director

ART Fertility Clinics LLC

研究点 (1)

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