Related Experiment Video
Updated: May 16, 2026

Vascular Organoid Generation from Human-Induced Pluripotent Stem Cells
Published on: December 13, 2024
Automated stem cell-derived organoid platforms for disease modeling
Xingrui Mou1, Nathan Dale1, Kiran Ramnarine1
1JAX-NYSCF (The Jackson Laboratory for Stem Cell Research), New York, NY, USA.
Abstract:
Complex diseases arise from genetic, environmental, and lifestyle factors, the combination of which is difficult to model. Conventional animal and 2D cell culture models have limitations in scalability, reproducibility, or human relevance. Human-induced pluripotent stem cells (iPSCs) can be differentiated into 3D organoids that better mimic human biology. However, organoid protocols can be lengthy, variable, and labor-intensive, limiting high-throughput applications. Suspension bioreactors and multilineage differentiation have improved yield and function, but challenges remain in tissue maturity, vascularization, and consistency. Automated high-throughput liquid handling systems are emerging as a solution, enabling large-scale, reproducible production. Here, we discuss how combining iPSC-derived organoids with automation is poised to transform disease modeling and drug development.

