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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

This protocol describes methodologies to establish simple and efficient embryo implantation in vitro model for evaluating the relevant molecules affecting the embryo implantation process.

Abstract

Embryo implantation is the first step in the establishment of a successful pregnancy. An in vitro model for embryo implantation is critical for basic biological research, drug development, and screening. This paper presents a simple, rapid, and highly efficient in vitro model for embryo implantation. In this protocol, we first introduce mouse blastocyst acquisition and human endometrial adenocarcinoma cells (Ishikawa) preparation for implantation, followed by the co-culture method for mouse embryos and Ishikawa cells. Finally, we conducted a study to assess the impact of varying concentrations of 17-β-estradiol (E2) and progesterone (P4) on embryo adhesion rates based on this model. Our findings revealed that high concentrations of E2 significantly reduced embryo adhesion, whereas the addition of progesterone could restore the adhesion rate. This model offers a simple and fast platform for evaluating and screening molecules involved in the adhesion process, such as cytokines, drugs, and transcription factors controlling implantation and endometrial receptivity.

Introduction

Embryo implantation, the initial step of successful pregnancy, is crucial for understanding its biological basis and addressing the challenges of infertility. However, ethical constraints pose significant limitations in collecting human clinical embryo samples, hampering research into the intricate interactions between human embryos and the endometrium during early pregnancy1. A profound comprehension of these complex mechanisms is vital for advancing fundamental biological research, drug discovery, and reproductive health.

Previous in vitro models employed adhesion models where monolayer human endometrial epithelial....

Protocol

Mouse handling and experimental studies were performed under protocols approved by the Animal Committee of the Shanghai Institute for Biomedical and Pharmaceutical Technologies. Ensure Safety Procedures: Always wear appropriate personal protective equipment (PPE) when handling chemicals or biological materials.

1. Acquisition of mouse embryos

NOTE: This section describes the process of obtaining mouse embryos. Adult female mice (6-8 weeks old, hybrid .......

Representative Results

In the process of assisted reproductive techniques, controlled ovarian hyperstimulation (COH) is a crucial step, leading to significantly elevated estrogen levels in patients by more than 10-20 times compared to natural cycles11. Given this context, we asked whether high serum estrogen concentrations impact embryo implantation during fresh embryo transfer. Based on this embryo implantation model, we studied the effects of various concentrations of E2 and P4 on embryo implantat.......

Discussion

The simplicity and rapidity of the proposed in vitro model for embryo implantation offer remarkable advantages for early-stage drug screening and other research applications. The straightforward protocol, coupled with the high-throughput nature of Ishikawa cell lines, makes it an ideal candidate for large-scale screens, particularly in the early stages of drug discovery. Liang13 found that TAGLN2 knockdown decreased the invasion ability of trophoblast cells. Green14

Acknowledgements

Our studies were supported by the National Natural Science Foundation of China (82171603), the Foundation of Shanghai Municipal Health Commission (202140341), the Science and Technology Commission of Shanghai Municipality (23JC1403803), and Innovation Promotion Program of NHC and Shanghai Key Labs, SIBPT (RC2023-02).

....

Materials

NameCompanyCatalog NumberComments
17-β-estradiolSIGMA3301Most potent mammalian estrogenic hormone
BD FalconBD353001Bacteriological Petri Dishes 35 x 10 mm style w/tight lid, crystal-grade virgin polystyrene, sterile
Biosafety CabinetESCOclass figure-materials-487BSCAseptic operations, making culture dishes, aliquoting reagents, etc
CO2 IncubatorThermo8000DHEmbryo culture
Culture plateCorning3506Cell culture
DMEM/F12Gibco1133032DMEM/F12 (1x), liquid 1:1,Contains L-glutamine and 15 mM HEPES buffer
Fetal Bovine SerumGibco10099141Fetal Bovine Serum, Qualified, Australia Origin
GelatinSIGMAG9391Type B, powder, BioReagent, suitable for cell culture
HCGNanjing AibeiM2520Sterilization reagent, intraperitoneal injection, 50 IU/mL
Hyaluronidase SIGMAV900833Reagent grade, powder 
KSOMMerckMR-020P-D(1x), Powder, w/o Phenol Red, 5 x 10 mL
L-glutamineGibco25030081L-glutamine-200 mM (100x), liquid
M2MerckMR-015-DEmbryoMax M2 Medium (1x), Liquid, with Phenol Red
Mineral oil SIGMAM8410Mineral oil is suitable for use as a cover layer to control evaporation and cross-contamination in various molecular biology applications
Penicillin-Streptomycin, liquidGibco1514012210,000 Units penicillin (base) and 10,000 units streptomycin (base), utilizing penicillin G (sodium salt) and streptomycin sulfate in 0.85% saline
PMSGNanjing AibeiM2620Sterilization reagent ,intraperitoneal injection, 50 IU/mL
ProgesteroneSIGMA5341Steroid hormone secreted by the corpus luteum during the latter half of the menstrual cycle
Sodium pyruvateGibco11360070Sodium pyruvate is commonly added to cell culture media as a carbon source in addition to glucose
StereomicroscopeOlympusSZX7Embryo retrieval and observation of embryo development

References

  1. Hannan, N. J., Paiva, P., Dimitriadis, E., Salamonsen, L. A. Models for study of human embryo implantation: choice of cell lines. Biol Reprod. 82 (2), 235-245 (2010).
  2. Li, H. Y., et al.

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Embryo ImplantationIn Vitro ModelBlastocystIshikawa Cells17 estradiolProgesteroneAdhesionEndometrial Receptivity

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