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Genetic Linkage

Organoids Model Spinal Cord Injuries

The spinal cord organoid on the left sports tiny nerve cell outgrowths after treatment with peptides that researchers call "dancing molecules." These tiny bits of human spinal cord serve as models for testing treatments for injuries. (Credit: Samuel I. Stupp/Northwestern University)


Organoids are tiny bits of organs nurtured in lab glassware from stem cells. I joke about them at Halloween, when a few drops of water on tiny sponge brain and heart precursors bloom into mini-organs.

 

A Bridge Between Animal Models and Clinical Testing

 

Real organoids are a brilliant tool to investigate biological processes and test new treatments. Induced pluripotent stem (iPS) cells are grown from a patient's skin fibroblast cells, providing a platform to test individualized interventions. And iPS cells are much closer to the human condition than a fruit fly, worm, zebrafish, rodent, or even a primate model.

 

Organoids aren't complete replicas of organs, but mimic how cells assemble into tissues of a specific organ, and how those tissues interact. They offer an increasingly important step between testing a treatment in an animal model and in people in clinical trials, saving time and funding and improving safety and efficacy.

 

The most recent report of a novel organoid to capture my attention is a mini human spinal cord, which researchers at Northwestern University created to model different types of injuries to test regenerative treatments. Like a spinal cord in a body, these miniature bits of humanity display inflammation, cell death, and the clumping of glial cells into impenetrable scar-like masses that can squelch nerve healing and regeneration.

 

To continue reading, go to DNA Science, where this post first appeared.

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