Brain imaging method is cable-free for improved social neuroscience study

The brain imaging method is based on a recent bioluminescence-based indicator of membrane voltage to record brain activity simultaneously in multiple, freely moving mice.

May 29th, 2019
In four mice, bioluminescence from the primary visual cortex (green) was observed at the same time (left); pseudo-colored locomotion trajectories, indicating velocity (center) and brain activity (right) of four mice freely interacting each other in the same cage, are also shown.
In four mice, bioluminescence from the primary visual cortex (green) was observed at the same time (left); pseudo-colored locomotion trajectories, indicating velocity (center) and brain activity (right) of four mice freely interacting each other in the same cage, are also shown.Professor Takeharu Nagai

Researchers at Osaka University (Osaka, Japan) have developed a brain imaging method based on a recent bioluminescence-based indicator of membrane voltage called LOTUS-V to record brain activity simultaneously in multiple, freely moving mice. The LOTUS-V bioluminescent probe is genetically encoded, which means that it is delivered to target cells noninvasively via a common gene expression system (the adeno-associated virus). Its signal is derived from cell membrane voltage changes, which reflect brain activity.

Existing electrophysiological and fluorescence-based brain imaging techniques in mice are generally invasive, require head fixes or cables, and are not suitable for long-term recordings. While there have been recent advances in imaging methods in freely moving animals, these are major limitations for researchers that are interested in the brain correlates of social behaviors.

"The LOTUS-V method reported brain activity in freely moving mice with a good sensitivity and without motion artifacts," says corresponding author Takeharu Nagai. "More importantly, it could measure dynamically changing brain activity in the primary visual cortex during social interactions."

LOTUS-V was applied to cells in the primary visual cortexan area known to respond to locomotor activity and visual stimulation. LOTUS-V signal changes reflected neural activity in response to visual stimuli and locomotor activity, as well as during interactions with other miceneural activity was significantly higher when a mouse approached others. Furthermore, the LOTUS-V signal was not affected by leaky signals emitted from other, nearby mice, which means that it reflected in vivo brain activity.

"Our method successfully detected activity of the superficial layer of the primary visual cortexthis is about 300 μm deep," says Shigenori Inagaki, first author of the study. "It will be important to test its applicability to recording in deeper brain regions."

While the temporal resolution of the LOTUS-V method was sufficient to investigate the dynamics of brain activity triggered by specific events, it is not yet superior to that of the fiber-based method.

"These results could be really exciting for social neurobiologists," Nagai says. "It is minimally invasive, doesn't require cables or head fixes, and is suitable for long-term recordings in freely moving animals, meaning it could be useful in a broad range of other research fields, too."

Full details of the work appear in the journal Scientific Reports

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