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 Concept Videos

Cleavage and Blastulation01:33

Cleavage and Blastulation

45.0K
After a large-single-celled zygote is produced via fertilization, the process of cleavage occurs while zygotes travel through the uterine tube. Cleavage is a mitotic cell division that does not result in growth. With each round of successive cell division, daughter cells get increasingly smaller.
45.0K
Zygotic Development And Stem Cell Formation01:10

Zygotic Development And Stem Cell Formation

5.1K
The development of all multicellular organisms starts with the fusion of haploid cells called sperm and egg to form a diploid zygote. A zygote is a totipotent cell that can develop into a complete organism. The zygote undergoes cell division or cleavage to form an 8-cell mass. Until this stage, the cells are spherical, loosely attached, and remain totipotent. Totipotent cells are capable of developing both the embryonic and the extraembryonic tissues. However, as they continue to divide, they...
5.1K
Gastrulation01:56

Gastrulation

57.0K
Gastrulation establishes the three primary tissues of an embryo: the ectoderm, mesoderm, and endoderm. This developmental process relies on a series of intricate cellular movements, which in humans transforms a flat, “bilaminar disc” composed of two cell sheets into a three-tiered structure. In the resulting embryo, the endoderm serves as the bottom layer, and stacked directly above it is the intermediate mesoderm, and then the uppermost ectoderm. Respectively, these tissue strata...
57.0K

You might also read

Related Articles

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

Sort by
Same author

Rewiring gene circuits to dissect oscillatory signaling dynamics.

Genes & development·2025
Same author

From genes to patterns: five key dynamical systems concepts to decode developmental regulatory mechanisms.

Development (Cambridge, England)·2025
Same author

NOTCH1 S2513 is critical for the regulation of NICD levels impacting the segmentation clock in hiPSC-derived PSM cells and somitoids.

Genes & development·2025
Same author

Signaling switches: Metabolism regulates gastruloid self-organization.

Cell stem cell·2025
Same author

Unravelling differential Hes1 dynamics during axis elongation of mouse embryos through single-cell tracking.

Development (Cambridge, England)·2024
Same author

Deciphering lineage specification during early embryogenesis in mouse gastruloids using multilayered proteomics.

Cell stem cell·2024

Related Experiment Video

Updated: Jun 18, 2025

Blastomere Explants to Test for Cell Fate Commitment During Embryonic Development
14:08

Blastomere Explants to Test for Cell Fate Commitment During Embryonic Development

Published on: January 26, 2013

15.2K

Setting the stage for embryo segmentation.

Katharina F Sonnen1

  • 1Hubrecht Institute-KNAW, University Medical Center Utrecht, Uppsalalaan 8 3584 CT Utrecht, the Netherlands.

Cell Stem Cell
|August 2, 2024
PubMed
Summary

Researchers developed a novel microfluidic system to precisely control morphogen gradients in human embryo segmentation models. This breakthrough allows for detailed study of developmental signaling pathways.

Area of Science:

  • Developmental Biology
  • Biotechnology
  • Microfluidics

Background:

  • Morphogen gradients are essential for orchestrating embryonic development.
  • Understanding human embryo segmentation requires precise control over signaling pathways.

Purpose of the Study:

  • To introduce a microfluidic system for external application of morphogen gradients.
  • To enable high-precision investigation of signaling during human embryo segmentation.

Main Methods:

  • Development of a novel microfluidic device.
  • Application of externally controlled morphogen gradients.
  • Utilizing an in vitro model of human embryo segmentation.

Main Results:

  • The microfluidic system allows for unprecedented precision in applying morphogen gradients.

More Related Videos

Plastic Embedding and Sectioning of Xenopus laevis Embryos
14:39

Plastic Embedding and Sectioning of Xenopus laevis Embryos

Published on: April 29, 2007

13.6K
A Semi-high-throughput Imaging Method and Data Visualization Toolkit to Analyze C. elegans Embryonic Development
06:49

A Semi-high-throughput Imaging Method and Data Visualization Toolkit to Analyze C. elegans Embryonic Development

Published on: October 29, 2019

6.7K

Related Experiment Videos

Last Updated: Jun 18, 2025

Blastomere Explants to Test for Cell Fate Commitment During Embryonic Development
14:08

Blastomere Explants to Test for Cell Fate Commitment During Embryonic Development

Published on: January 26, 2013

15.2K
Plastic Embedding and Sectioning of Xenopus laevis Embryos
14:39

Plastic Embedding and Sectioning of Xenopus laevis Embryos

Published on: April 29, 2007

13.6K
A Semi-high-throughput Imaging Method and Data Visualization Toolkit to Analyze C. elegans Embryonic Development
06:49

A Semi-high-throughput Imaging Method and Data Visualization Toolkit to Analyze C. elegans Embryonic Development

Published on: October 29, 2019

6.7K
  • The system facilitates the study of developmental signaling in human embryo segmentation models.
  • Conclusions:

    • The developed microfluidic system is a powerful tool for studying embryonic development.
    • This technology offers new possibilities for investigating morphogen gradient roles with high accuracy.