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This protocol describes methodologies to establish simple and efficient embryo implantation in vitro model for evaluating the relevant molecules affecting the embryo implantation process.
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.
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....
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 .......
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.......
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
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).
....Name | Company | Catalog Number | Comments |
17-β-estradiol | SIGMA | 3301 | Most potent mammalian estrogenic hormone |
BD Falcon | BD | 353001 | Bacteriological Petri Dishes 35 x 10 mm style w/tight lid, crystal-grade virgin polystyrene, sterile |
Biosafety Cabinet | ESCO | class BSC | Aseptic operations, making culture dishes, aliquoting reagents, etc |
CO2 Incubator | Thermo | 8000DH | Embryo culture |
Culture plate | Corning | 3506 | Cell culture |
DMEM/F12 | Gibco | 1133032 | DMEM/F12 (1x), liquid 1:1,Contains L-glutamine and 15 mM HEPES buffer |
Fetal Bovine Serum | Gibco | 10099141 | Fetal Bovine Serum, Qualified, Australia Origin |
Gelatin | SIGMA | G9391 | Type B, powder, BioReagent, suitable for cell culture |
HCG | Nanjing Aibei | M2520 | Sterilization reagent, intraperitoneal injection, 50 IU/mL |
Hyaluronidase | SIGMA | V900833 | Reagent grade, powder |
KSOM | Merck | MR-020P-D | (1x), Powder, w/o Phenol Red, 5 x 10 mL |
L-glutamine | Gibco | 25030081 | L-glutamine-200 mM (100x), liquid |
M2 | Merck | MR-015-D | EmbryoMax M2 Medium (1x), Liquid, with Phenol Red |
Mineral oil | SIGMA | M8410 | Mineral oil is suitable for use as a cover layer to control evaporation and cross-contamination in various molecular biology applications |
Penicillin-Streptomycin, liquid | Gibco | 15140122 | 10,000 Units penicillin (base) and 10,000 units streptomycin (base), utilizing penicillin G (sodium salt) and streptomycin sulfate in 0.85% saline |
PMSG | Nanjing Aibei | M2620 | Sterilization reagent ,intraperitoneal injection, 50 IU/mL |
Progesterone | SIGMA | 5341 | Steroid hormone secreted by the corpus luteum during the latter half of the menstrual cycle |
Sodium pyruvate | Gibco | 11360070 | Sodium pyruvate is commonly added to cell culture media as a carbon source in addition to glucose |
Stereomicroscope | Olympus | SZX7 | Embryo retrieval and observation of embryo development |
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