CNS-3D Plasticity Organoids

Assess drug candidate effects on human neural plasticity and learning-related responses. Cognitive Biomarker Services for CNS-3D Plasticity Organoids provide a functional, human alternative to conventional static biomarkers.
CNS-3D Myelinated Organoids Biology Image
CNS-3D Plasticity Organoids pair two human iPSC-derived cortical organoids in a custom electrode array plate, forming a connected neural network trainable through electrical stimulation. This model enables functional assessment of drug candidate effects on learning-related pathways, including network potentiation and synaptic plasticity.

Functional electrophysiological data can be combined with conventional molecular and structural endpoints for an integrated evaluation of drug candidate effects on learning-related circuit function. This enables researchers developing therapies for cognitive decline and neurodegenerative disease to assess drug effects on learning response, rather than relying solely on static disease biomarkers. CNS-3D Plasticity Organoids are available through Cognitive Biomarker Services for end-to-end study design, execution, and analysis.

Key Advantages

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Trainable Human
Neural Model

Pair two human iPSC-derived cortical organoids into a connected neural network trainable through electrical stimulation.
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Functional Learning
Insights

Measure drug effects on learning-related plasticity rather than static disease biomarkers.
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Flexible Study
Designs

Combine any CNS-3D Organoid type to study plasticity in disease-relevant contexts.

Network Potentiation

Evaluate drug candidate effects on network potentiation, a core mechanism of human learning and memory.

By measuring evoked network activity before and after repeated stimulation, CNS-3D Plasticity Organoids capture synaptic potentiation, the mechanism underlying learning and memory. Daily training induces a significant, progressive, and pharmacologically tunable increase in evoked response, providing a human-relevant assay to evaluate drug candidates that enhance, protect, or restore learning-related pathways.
Daily training stimulation drives progressive network potentiation in CNS-3D Plasticity Organoids, an effect accelerated by BDNF and abolished by NMDA-receptor blockade (AP-5).

Neural Plasticity

Evaluate drug candidate effects on reward-based learning in a virtual maze-navigation task.

In this assay, CNS-3D Plasticity Organoids navigate a virtual maze, using evoked network activity to drive movement and receiving reward or penalty stimulation based on performance—a human neural model analog to classic rodent maze-learning assays. Real-time feedback training improves maze performance, including points scored and survival time, offering a human-relevant assay to evaluate drug candidate enhancement or impairment of learning.
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Trained CNS-3D Plasticity Organoids show increasing points scored and survival time across five days of training, while untrained organoids show little change.

Services

Scientific Alignment

Meet with expert scientists to define your research question, study objectives, decision criteria, and success measures.

Experimental Design

Our scientists translate your research objectives into a detailed experimental plan designed to generate decision-ready data.

Study Execution

Your study is executed by using established workflows, with regular project updates throughout the engagement.

Data Review & Reporting

Receive a detailed study report and meet with our scientists to review results, discuss key findings, and align on next steps.

CNS-3D Myelinated Organoid Resources

Explore resources for evaluating cognitive biomarkers in CNS-3D Plasticity Organoids.

Ready to get started?

Connect with our team to discuss your research goals and identify the 28bio organoid model best aligned to your study aims.