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From stem cells to functional tissue

We differentiate human iPSCs into 3D pancreatic microtissues that replicate the structure and function of native human islets.

iPSC differentiation process

1

iPSC expansion

Human iPSCs are expanded under defined, feeder-free conditions to ensure consistent starting material.

2

Directed differentiation

A multi-stage protocol guides iPSCs through definitive endoderm, pancreatic progenitor, and endocrine precursor stages.

3

3D aggregation

Endocrine cells self-organize into 3D microtissues (pseudoislets) that mimic the architecture of native pancreatic islets.

4

Functional maturation

Mature microtissues exhibit glucose-stimulated insulin secretion (GSIS), the gold-standard functional readout.

How we compare

2D cell lines Animal models StemX microtissues
Physiological relevanceLowModerateHigh
Human translationPoorPoor (5%)Direct
ReproducibilityHighLowHigh
ThroughputHighLowMedium-High
Ethical concernsNoneSignificantNone
3D architectureNoYesYes

Applications

Drug screening

Test compound efficacy and toxicity on human pancreatic tissue. GSIS, viability, and multi-parameter readouts.

Therapy validation

Validate transduction efficiency and functional rescue in a human 3D tissue context. Includes toxicity assessment.

Disease modeling

Model metabolic disease phenotypes using patient-derived or gene-edited iPSC lines in a physiologically relevant format.

Want to learn more about our platform?

We are happy to walk you through our technology, discuss your application, or design a pilot study.