Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Blastocyst culture.

D Randall Armant1

  • 1Department of Obstetrics & Gynecology, Wayne State University School of Medicine, Detroit, MI, USA.

Methods in Molecular Medicine
|October 28, 2005
PubMed
Summary
This summary is machine-generated.

This study details a mouse blastocyst culture method to observe early embryonic development. It enables researchers to study peri-implantation events and trophoblast function in vitro.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Human placentation: foundations and implications for reproductive endocrinology and infertility.

Systems biology in reproductive medicine·2025
Same author

Toxicity assessments of selected trichloroethylene and perchloroethylene metabolites in three in vitro human placental models.

Reproductive toxicology (Elmsford, N.Y.)·2022
Same author

Transcriptional profiling of the response to the trichloroethylene metabolite S-(1,2-dichlorovinyl)-L-cysteine revealed activation of the eIF2α/ATF4 integrated stress response in two in vitro placental models.

Archives of toxicology·2021
Same author

Baboon placental heparin-binding epidermal growth factor-like growth factor.

Reproduction (Cambridge, England)·2020
Same author

Endocervical trophoblast for interrogating the fetal genome and assessing pregnancy health at five weeks.

European journal of medical genetics·2019
Same author

Rosiglitazone augments antioxidant response in the human trophoblast and prevents apoptosis†.

Biology of reproduction·2018
Same journal

Erratum to: Immunotherapeutic Approach to Cancer with Cutaneous DNA Vaccination.

Methods in molecular medicine·2015
Same journal

Methods for cancer gene therapy using tumor suppressor genes.

Methods in molecular medicine·2014
Same journal

Suppression of the human carcinoma phenotype by an antioncogene ribozyme.

Methods in molecular medicine·2014
Same journal

Methods for the use of stromal cells for therapeutic gene therapy.

Methods in molecular medicine·2014
Same journal

Methods for adenovirus-mediated gene transfer to synovium in vivo.

Methods in molecular medicine·2014
Same journal

Methods for gene transfer to synovium.

Methods in molecular medicine·2014
See all related articles

Area of Science:

  • Developmental Biology
  • Reproductive Science
  • Cell Biology

Background:

  • In vitro blastocyst culture models are crucial for studying peri-implantation development, a process difficult to observe in vivo.
  • These models allow controlled examination of embryonic interactions with the microenvironment.
  • Key in utero events like expansion, hatching, and matrix adhesion can be mimicked and studied.

Purpose of the Study:

  • To describe a standardized method for obtaining and culturing mouse blastocysts.
  • To correlate in vitro morphological changes during blastocyst culture with in utero development.
  • To present quantitative assays for monitoring trophoblast development during peri-implantation in vitro.

Main Methods:

  • Isolation and in vitro culture of mouse blastocysts.

Related Experiment Videos

  • Morphological assessment of blastocysts during culture.
  • Development and application of quantitative assays for trophoblast function.
  • Main Results:

    • The described method allows for successful blastocyst culture and observation of key developmental events.
    • Morphological changes in vitro correlate with established in utero developmental milestones.
    • Quantitative assays provide reliable measures of trophoblast behavior and peri-implantation potential.

    Conclusions:

    • In vitro mouse blastocyst culture is a valuable tool for understanding peri-implantation development.
    • This method facilitates detailed study of trophoblast biology and its interaction with the uterine environment.
    • The quantitative assays enable robust assessment of developmental processes critical for successful implantation.