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Related Concept Videos

EPS and iPS Cells in Disease Research01:21

EPS and iPS Cells in Disease Research

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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,...
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Updated: Oct 10, 2025

Robust and Highly Reproducible Generation of Cortical Brain Organoids for Modelling Brain Neuronal Senescence In Vitro
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Modeling Developmental Brain Diseases Using Human Pluripotent Stem Cells-Derived Brain Organoids - Progress and

Afrin Bhattacharya1, Wendy W Y Choi2, Julien Muffat3

  • 1Program in Developmental and Stem Cell Biology, The Hospital for Sick Children, 686 Bay Street, Toronto, ON M5G 0A4, Canada; The University of Toronto, Department of Molecular Genetics, 1 King's College Circle, Toronto, ON M5S 1A8, Canada.

Journal of Molecular Biology
|December 9, 2021
PubMed
Summary

Brain organoids offer a novel in vitro model for studying developmental brain diseases, overcoming limitations of traditional methods. These human stem cell-derived structures provide insights into disease mechanisms and potential treatments.

Keywords:
braindevelopmentdisorderorganoidstechnology

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Area of Science:

  • Neuroscience
  • Developmental Biology
  • Stem Cell Research

Background:

  • Developmental brain diseases stem from early life genetic or environmental factors.
  • Etiology and treatment of these conditions remain poorly understood due to disease heterogeneity and limitations of animal models.

Purpose of the Study:

  • To review the application of brain organoids in modeling human developmental brain diseases.
  • To discuss current progress, challenges, and future directions in this field.

Main Methods:

  • Utilizing brain organoids derived from human pluripotent stem cells.
  • Integrating advanced techniques like genome editing, tissue engineering, electrophysiology, and multi-omics analysis.

Main Results:

  • Brain organoids successfully recapitulate key developmental milestones of the early human brain.
  • These models offer valuable insights into the cellular and molecular mechanisms underlying normal and pathological brain development.

Conclusions:

  • Brain organoid technology represents a significant advancement in studying developmental brain diseases.
  • Further technological development is crucial to fully realize the potential of brain organoids for understanding and treating these complex conditions.