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Completed

NCT Number: NCT04865367

How Secreted-embryo-derived Trypsin Initiates, Maintains and Terminates Ca2+ Signals in Uterine Epithelial Cells

To develop a deeper understanding of endometrial-embryo crosstalk through basic research, uncover therapeutic targets and to improve reproductive outcome.

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Key information

Age range

18 year–36 year

Sex eligibility

Female

Study type

Observational

Primary location

ART Fertility Clinics LLC

Abu Dhabi, 60202, United Arab Emirates

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Couples with primary / secondary infertility who are planned to undergo ICSI treatment with PGT-A
  • Age of each partner above 18 years

Exclusion criteria

  • 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)

Treatment and study plan

Exposure to culture media

Other

Exposure to culture media

Primary outcomes

  1. Change in markers of protein

    Time frame: 1 day

    Change in markers of protein (PAR2, (p) and SGK1, NFkB, ORAI1-3 and STIM1-2 and COX2) using Western blotting

  2. Change in peak and slope levels of intracellular calcium

    Time frame: 1 day

    Change in peak and slope levels of intracellular calcium

  3. Change in morphohology of cells after incubation with embryo media

    Time frame: 1 day

    Change in morphohology of cells after incubation with embryo media

Secondary outcomes

  1. Performance of ICSI

    Time frame: 1 day

    Defined on day 0 as the number of injected oocytes/number of COCs assigned to the ICSI group

  2. Embryo quality on day 3

    Time frame: 1 day

    Defined by the number of blastomeres and their division pattern, fragmentation, presence of compaction, vacuoles, granulation and nuclei

  3. Embryo quality on day 5 (Gardner and Schoolcraft,1999)

    Time frame: 1 day

    Gardner and Schoolcraft,1999) defined by:

    • The expansion stage of the blastocyst
    • Quality of the ICM and TE
    • Day on which the biopsy is performed (day 5,6 or 7)
    • Pregnancy outcomes (miscarriages/ectopic pregnancy/neonatal outcome)

Sponsors and collaborators

Lead sponsor

ART Fertility Clinics LLC

Other

Collaborators

  • University Women's Hospital Tübingen

Registry information

Official study title

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

Acronym: Ca2+

Important dates

Study start
2021
Primary completion
2023
Study completion
2023
First posted
Apr 29, 2021
Registry last updated
Jul 17, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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