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

Embryonic Stem Cells00:58

Embryonic Stem Cells

29.0K
Embryonic stem (ES) cells are undifferentiated pluripotent cells, meaning they can produce any cell type in the body. This gives them tremendous potential in science and medicine since they can generate specific cell types for use in research or to replace body cells lost due to damage or disease.
29.0K
Induced Pluripotent Stem Cells01:13

Induced Pluripotent Stem Cells

24.4K
Stem cells are undifferentiated cells that divide and produce different types of cells. Ordinarily, cells that have differentiated into a specific cell type are post-mitotic—that is, they no longer divide. However, scientists have found a way to reprogram these mature cells so that they “de-differentiate” and return to an unspecialized, proliferative state. These cells are also pluripotent like embryonic stem cells—able to produce all cell types—and are therefore...
24.4K

You might also read

Related Articles

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

Sort by
Same author

Coordinated regulation of mRNA translation and stability by ZC3H7A and ZC3H7B RNA-binding proteins.

Cell reports·2026
Same author

Direct Mapping of CDK2 Substrates in Embryonic Stem Cells Uncovers an AP-Site Repair Mechanism via HMCES Phosphorylation.

bioRxiv : the preprint server for biology·2026
Same author

Quantitative CDK2 Dynamics Are Linked to Cell Fate Decisions in Differentiating Trophoblast Stem Cells.

bioRxiv : the preprint server for biology·2026
Same author

E2F1 induces a G0-G1 reentry transcriptional program without changing chromatin accessibility.

bioRxiv : the preprint server for biology·2025
Same author

Application of CRISPR-Based Epigenome Editing Tools for Engineering Programmable Embryo Models.

Methods in molecular biology (Clifton, N.J.)·2025
Same author

Three-dimensional culture in a bioengineered matrix and somatic cell complementation to improve growth and survival of bovine preantral follicles.

Journal of assisted reproduction and genetics·2025
Same journal

Horizontal transfer of mitochondria in cancer: The physiology reborn in disease?

Trends in cell biology·2026
Same journal

Spindle errors: A stress test for epithelial robustness.

Trends in cell biology·2026
Same journal

Multicellular ecosystems: Linking cellular diversity to tissue function and disease.

Trends in cell biology·2026
Same journal

Orchestrating the signaling-bias at the protease-activated receptor, PAR1.

Trends in cell biology·2026
Same journal

Crashing by design: Utilizing DNA damage for MCC differentiation.

Trends in cell biology·2026
Same journal

The value of a shared lab: Our insights.

Trends in cell biology·2026
See all related articles

Related Experiment Video

Updated: Sep 9, 2025

Patterning the Geometry of Human Embryonic Stem Cell Colonies on Compliant Substrates to Control Tissue-Level Mechanics
10:04

Patterning the Geometry of Human Embryonic Stem Cell Colonies on Compliant Substrates to Control Tissue-Level Mechanics

Published on: September 28, 2019

8.4K

Understanding human embryogenesis by building programmable stem cell-based models.

Carly Guiltinan1, Gerrald A Lodewijk1, Sayaka Kozuki1

  • 1Department of Biomolecular Engineering, University of California Santa Cruz, Santa Cruz, CA, USA; Genomics Institute, University of California Santa Cruz, Santa Cruz, CA, USA; Institute for the Biology of Stem Cells, University of California Santa Cruz, Santa Cruz, CA, USA.

Trends in Cell Biology
|September 3, 2025
PubMed
Summary
This summary is machine-generated.

New stem cell-based embryo models mimic early development. Epigenome editing created programmed mouse embryos, offering potential for engineering human embryogenesis models.

Keywords:
CRISPR activationembryo modelsepigenome editingstem cells

More Related Videos

Protocol for Human Blastoids Modeling Blastocyst Development and Implantation
12:09

Protocol for Human Blastoids Modeling Blastocyst Development and Implantation

Published on: August 10, 2022

6.6K
Reprogramming Primary Amniotic Fluid and Membrane Cells to Pluripotency in Xeno-free Conditions
09:34

Reprogramming Primary Amniotic Fluid and Membrane Cells to Pluripotency in Xeno-free Conditions

Published on: November 27, 2017

9.4K

Related Experiment Videos

Last Updated: Sep 9, 2025

Patterning the Geometry of Human Embryonic Stem Cell Colonies on Compliant Substrates to Control Tissue-Level Mechanics
10:04

Patterning the Geometry of Human Embryonic Stem Cell Colonies on Compliant Substrates to Control Tissue-Level Mechanics

Published on: September 28, 2019

8.4K
Protocol for Human Blastoids Modeling Blastocyst Development and Implantation
12:09

Protocol for Human Blastoids Modeling Blastocyst Development and Implantation

Published on: August 10, 2022

6.6K
Reprogramming Primary Amniotic Fluid and Membrane Cells to Pluripotency in Xeno-free Conditions
09:34

Reprogramming Primary Amniotic Fluid and Membrane Cells to Pluripotency in Xeno-free Conditions

Published on: November 27, 2017

9.4K

Area of Science:

  • Developmental Biology
  • Stem Cell Biology
  • Epigenetics

Background:

  • Studying early human development is challenging due to ethical and technical limitations.
  • Stem cell-based embryo models offer a promising alternative for investigating developmental processes.
  • Recent advances in epigenome editing have enabled the creation of programmed embryonic models.

Purpose of the Study:

  • To discuss the recent generation of programmed mouse embryo models using epigenome editing.
  • To explore the potential of these advancements for creating engineering models of human embryogenesis.

Main Methods:

  • Utilizing epigenome editing techniques to activate endogenous regulatory elements.
  • Generating programmed mouse embryo models.

Main Results:

  • Successful creation of programmed mouse embryo models through targeted activation of regulatory elements.
  • Demonstration of a novel approach to recapitulate aspects of early development.

Conclusions:

  • The development of programmed embryo models represents a significant achievement in developmental biology.
  • These models hold considerable potential for advancing our understanding of human embryogenesis and related disorders.
  • Future research can focus on translating these findings to engineer more sophisticated human embryonic models.