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

Induced Pluripotent Stem Cells01:13

Induced Pluripotent Stem Cells

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 called induced pluripotent stem...
iPS Cell Differentiation01:22

iPS Cell Differentiation

The ability of induced pluripotent stem cells or iPSCs to differentiate into most body cell types has stimulated repair and regenerative medicine research over the past few decades. iPSC-derived blood cells, hepatocytes, beta islet cells, cardiomyocytes, neurons, and other cell types can repair injuries or regenerate damaged tissue in diseases such as diabetes and neurodegenerative disorders.
EPS and iPS Cells in Disease Research01:21

EPS and iPS Cells in Disease Research

Embryonic and induced pluripotent stem cells are excellent models for disease research because of their ability to self-renew and differentiate into most cell types. Somatic cells from a patient are isolated and reprogrammed into induced pluripotent stem cells or iPSCs. These iPSCs are later differentiated into the desired cell type, which mirrors the diseased cell of the patient. In this way, disease models have been created for investigating diseases such as Down syndrome, type I diabetes,...

You might also read

Related Articles

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

Sort by
Same author

Ligand-Driven Supramolecular Assembly of Gold Nanoclusters with Ultralong Lifetime and Large Stokes Shift for High-Efficiency Electrochemiluminescence.

Analytical chemistry·2026
Same author

Subacute Exposure to Macrocyclic Lactone Insecticides Induces Parkinson's Disease-like Motor Deficits and Neuropathology in Mice.

Environmental science & technology·2026
Same author

Multi-model analysis of the combined toxic effects of ultrafine carbon black and amisulbrom on A549 Cells.

Scientific reports·2026
Same author

A multimodal viro-immunotherapy strategy for glioblastoma.

Molecular therapy. Oncology·2026
Same author

Herbal pairs containing Paeoniae Radix Alba: A review of pharmacological activities, clinical applications, and data mining analysis of compatibility patterns.

Journal of ethnopharmacology·2026
Same author

Exclusive enteral nutrition and infliximab combination therapy are superior to monotherapy in inducing endoscopic response in active adult Crohn's disease.

Therapeutic advances in gastroenterology·2026

Related Experiment Video

Updated: May 8, 2026

Generation of Standardized and Reproducible Forebrain-type Cerebral Organoids from Human Induced Pluripotent Stem Cells
10:25

Generation of Standardized and Reproducible Forebrain-type Cerebral Organoids from Human Induced Pluripotent Stem Cells

Published on: January 23, 2018

21.4K

Generating Homogeneous Brain Organoids from Human iPSCs.

Xianwei Chen1, Yanhong Shi2

  • 1Department of Neurodegenerative Diseases, Beckman Research Institute of City of Hope, Duarte, CA, USA.

Methods in Molecular Biology (Clifton, N.J.)
|April 17, 2024
PubMed
Summary

Developing consistent, high-yield human brain organoids is crucial for studying neurological diseases. This new method uses large-scale embryoid body generation and quality control to improve brain organoid production for research.

Keywords:
Alzheimer’s diseaseBrain organoidsDifferentiationDisease modelingEmbryoid bodies (EBs)Induced pluripotent stem cells (iPSCs)Neurological diseasesPluripotent stem cells (PSCs)

More Related Videos

A Static Self-Directed Method for Generating Brain Organoids from Human Embryonic Stem Cells
08:30

A Static Self-Directed Method for Generating Brain Organoids from Human Embryonic Stem Cells

Published on: March 4, 2020

8.8K
Brain Organoid Generation from Induced Pluripotent Stem Cells in Home-Made Mini Bioreactors
10:16

Brain Organoid Generation from Induced Pluripotent Stem Cells in Home-Made Mini Bioreactors

Published on: December 11, 2021

5.5K

Related Experiment Videos

Last Updated: May 8, 2026

Generation of Standardized and Reproducible Forebrain-type Cerebral Organoids from Human Induced Pluripotent Stem Cells
10:25

Generation of Standardized and Reproducible Forebrain-type Cerebral Organoids from Human Induced Pluripotent Stem Cells

Published on: January 23, 2018

21.4K
A Static Self-Directed Method for Generating Brain Organoids from Human Embryonic Stem Cells
08:30

A Static Self-Directed Method for Generating Brain Organoids from Human Embryonic Stem Cells

Published on: March 4, 2020

8.8K
Brain Organoid Generation from Induced Pluripotent Stem Cells in Home-Made Mini Bioreactors
10:16

Brain Organoid Generation from Induced Pluripotent Stem Cells in Home-Made Mini Bioreactors

Published on: December 11, 2021

5.5K

Area of Science:

  • Neuroscience
  • Stem Cell Biology
  • Developmental Biology

Background:

  • Human brain tissues are inaccessible for research, necessitating advanced in vitro models.
  • Human induced pluripotent stem cell (hiPSC)-derived brain organoids offer a promising model for studying brain development and diseases.
  • Current challenges include generating a large quantity of consistent brain organoids for disease modeling.

Purpose of the Study:

  • To describe a novel method for generating high-yield, consistent brain organoids.
  • To facilitate the study of human brain development and neurological disorders using improved in vitro models.

Main Methods:

  • Combines large-scale embryoid body (EB) generation.
  • Incorporates a quality control screening step during differentiation.
  • Focuses on robust generation of brain organoids from hiPSCs.

Main Results:

  • Achieved high-yield production of brain organoids.
  • Demonstrated high consistency in the generated brain organoids.
  • Established a robust method for brain organoid generation.

Conclusions:

  • The described method provides a reliable approach for generating brain organoids.
  • This advancement supports the study of human brain development and neurological disease modeling.
  • Enables more consistent and scalable research into brain disorders.