Related Experiment Video
Updated: Oct 17, 2026

Generation of a Human iPSC-Based Blood-Brain Barrier Chip
Published on: March 2, 2020
Programming brain endothelial identity: Transcription factor and genome engineering approaches to improve
Roy W Hwang1, Ying Betty Li2, Richard Marcotte3
1Human Health Therapeutics Research Center, Translational Biosciences, National Research Council of Canada, Ottawa, ON, Canada; Department of Cellular and Molecular Medicine, Faculty of Medicine, University of Ottawa, Ottawa, ON, Canada.
Abstract:
Human induced pluripotent stem cell-derived brain endothelial-like cells (iBECs) serve as important human relevant in vitro blood-brain barrier (BBB) models for evaluating central nervous system (CNS)-targeted therapies. However, conventional differentiation protocols often generate heterogeneous populations constrained by incomplete endothelial maturation. Overcoming these limitations requires precise control over developmental gene regulatory networks throughout differentiation. This review examines transcription factor-based forward reprogramming strategies designed to induce brain endothelial cell fate and prime BBB identity. Integrating these approaches with novel genome engineering tools enables the rational design of next generation BBB models with improved physiological fidelity and predictive power for CNS therapeutic discovery and validation.
More Related Videos
08:04Derivation, Expansion, Cryopreservation and Characterization of Brain Microvascular Endothelial Cells from Human Induced Pluripotent Stem Cells
Published on: November 19, 2020
06:19Reconstruction of the Blood-Brain Barrier In Vitro to Model and Therapeutically Target Neurological Disease
Published on: October 20, 2023
Related Concept Videos
EPS and iPS Cells in Disease Research
Somatic to iPS Cell Reprogramming
iPS Cell Differentiation
Induced Pluripotent Stem Cells