Easily study myelination

Dr. Dalinda Liazoghli, McGill University, while studying myelination of DRG axons.


With Ananda microfluidic devices, Dr. Dalinda Liazoghli was able to grow DRG neurons for several weeks. She obtained robust axonal myelination and the formation of internodes. The devices allowed for easy access and identification of neurites as well as of the associated myelinating cells. These properties of the devices contribute to studies on the process of myelination and the effects of axonal damage on this process.



Regular neuronal cell culture to study myelination of DRG neurons in vitro without Ananda Devices' neuronal microfluidic devices.

Without Ananda Devices

Neuronal cell culture to study myelination of DRG neurons in vitro with Ananda Devices' neuronal microfluidic devices.

With Ananda Devices
Watch video

Picture of neurons' organization in the Central Nervous System

In the CNS


Studying myelination of DRG neurons in vitro

To study myelination of DRG neurons, Dr. Liazoghli needed a co-culture cell system that facilitated the visualization of axons and the development of myelin in vitro. Regular cell culture dishes do not always allow for the growth of multiple long axons for many weeks that is ideal for myelination studies.

For more details please refer to: Liazoghli et al., ACS Chemical Neuroscience 2012.