Skip to content

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

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04865367
Acronym
Ca2+
Enrollment
81
Registered
2021-04-29
Start date
2021-11-04
Completion date
2023-05-15
Last updated
2024-07-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aneuploidy, Infertility, Infertility, Female

Keywords

IVF, RNA, Ca2+, embryo, media

Brief summary

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

Detailed description

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.

Interventions

OTHERExposure to culture media

Exposure to culture media

Sponsors

University Women's Hospital Tübingen
CollaboratorOTHER
ART Fertility Clinics LLC
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 36 Years
Healthy volunteers
Yes

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)

Design outcomes

Primary

MeasureTime frameDescription
Change in markers of protein1 dayChange 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 calcium1 dayChange in peak and slope levels of intracellular calcium
Change in morphohology of cells after incubation with embryo media1 dayChange in morphohology of cells after incubation with embryo media

Secondary

MeasureTime frameDescription
Performance of ICSI1 dayDefined on day 0 as the number of injected oocytes/number of COCs assigned to the ICSI group
Embryo quality on day 31 dayDefined by the number of blastomeres and their division pattern, fragmentation, presence of compaction, vacuoles, granulation and nuclei
Embryo quality on day 5 (Gardner and Schoolcraft,1999)1 dayGardner 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)

Countries

United Arab Emirates

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026