Brain Tissue Kept Alive for Weeks on an Artificial Membrane

To solve this problem, RIKEN BDR scientists developed a microfluidic device using polydimethylsiloxane (PDMS), the material often used as a defoamer in over-the-counter drugs. The device has a semi-permeable channel surrounded by an artificial membrane and solid PDMS walls. Rather than constantly being immersed in fluid, the tissue benefited from having the culture medium circulate within the microchannel and pass through the permeable membrane, which allowed proper gas exchange. This sounds simple, but finding the optimal settings proved challenging. As first author Nobutoshi Ota notes, “Controlling the medium flow was difficult because the microchannel that formed between the PDMS walls and the porous membrane was unusual. However, we had success after trial and error modifications to the porous membrane and adjustments of the inlet/outlet flow rates.”

The team tested the device using tissue from the mouse suprachiasmatic nucleus, a complex part of the brain that governs circadian rhythms. The mice themselves were knock-in mice in which circadian rhythm activity in the brain was linked to the production of a highly fluorescent protein. By measuring the level of bioluminescence coming from the brain tissue, they were able to see that tissue kept alive by their system stayed active and functional for over 25 days with nice circadian activity. In contrast, neural activity in tissue kept in a conventional culture decreased by 6% after only 10 hours.

This new method will have several benefits. In the short-term, it will be useful in observing biological development and testing how tissues respond to drugs. The long-term benefits are also clear. “This method can be used for more than explanted tissues from animals,” says Ota. “It will also improve research into organogenesis through long-term culturing and observation which is necessary for growing tissue and organs.”

Indeed, the team is currently planning long-term experiments using their system to observe the formation of blood vessels and the movements of cells during organoid formation.

This study was published in the journal Analytical Sciences.

Contacts and sources:
Yo Tanaka Laboratory for Integrated Biodevices