Novel Imaging Method to Visualize Respiratory Activity of 3D Tissue Models

Cells breathe, to an extent, exchanging gases, taking in energy sources from the environment and processing it. Now, researchers from Tohoku University have shone a light on the process in a new way.

Novel Imaging Method to Visualize Respiratory Activity of 3D Tissue Models

Cells breathe, to an extent, exchanging gases, taking in energy sources from the environment and processing it. Now, researchers from Tohoku University in Japan have shone a light on the process in a new way.

Their demonstrated visualization method in model systems was made available online on March 12th in Biosensors and Bioelectronics, ahead of the June print edition.

The researchers used spheroids - cultured cells within a close-to-natural environment - to mimic a biological tissue using mesenchymal stem cells (MSCs). Due to MCSs' ability to self-renew and differentiate into various tissues, they are of significant interest for use in regenerative medicine and to test different therapeutics in different tissue models.

They settled the spheroids on a gold electrode dosed in luminescent solution. The researchers applied stepped electric potential - the energy needed to convert oxygen - to the set up where the solution was then oxidized sensitized to produce luminescent, which is dependent on oxygen concentration. The spheroids glowed brightly, surrounded by a ring of darkness where oxygen concentration was low due to gas exchanges. They call the process potential step-based electrochemiluminescence (ECL) imaging.

Spheroids were settled on the gold electrode with a luminescent solution. When the potential steps were applied, the spheroids were brightly visualized. The dark area around the spheroids indicates a decrease in luminescence attributed to low O2 concentration, caused by the respiratory activity of the spheroids.

"As living spheroids consume oxygen to produce energy, the respiratory activity was elegantly visualized by the distribution of luminescence around the spheroids," said Kaoru Hiramoto of the JSPS Research Fellowship for Young Scientists, who developed the ECL imaging system.

The researchers used a digital camera to visualize multiple spheroids with a single shot, demonstrating both the high spatial resolution of their system, as well as the low background noise.

"The system offers high throughput analysis of spheroids, in addition to highly improving resolution of the images compared to conventional electrode array devices," said co-corresponding authors Kosuke Ino and Hitoshi Shiku, assistant professor and professor in the Graduate School of Engineering, Tohoku University. "The system offers novel insights into electrochemical devices and imaging systems for cell spheroids."

ECL imaging is still in the development phase, the researchers said. They plan to improve the sensitivity and selectivity, as well as analyze other data that might be collected in the system, such as cellular metabolites attached to the electrode. They also plan to use the system to investigate more complicated biological models, as well as patient-derived cell spheroids.

"To the best of our knowledge, this is the first attempt to visualize the respiratory activity of spheroids by direct conversion of oxygen concentration into ECL imaging," Ino said. "The features of the proposed system - high spatial resolution with the ability for simultaneous imaging of multiple spheroids - are promising for transplantation research and drug screening utilizing cell spheroids."

Contact:
Kosuke Ino
Graduate School of Engineering, Tohoku University
Email: [email protected]

Hitoshi Shiku
Graduate School of Engineering, Tohoku University
Email: [email protected]
Website: https://www.che.tohoku.ac.jp/~est/index_English.html

 

Published: 27 Apr 2021

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Title: Electrochemiluminescence imaging of respiratory activity of cellular spheroids using sequential potential steps
Authors: Kaoru Hiramoto, Kosuke Ino, Keika Komatsu, Yuji Nashimoto, Hitoshi Shiku
Journal:Biosensors and Bioelectronics
DOI: 10.1016/j.bios.2021.113123

Funding information:

Grants-in-Aid for Scientific Research (Nos. 20H00619, 18H01840, and 18H01999), a Grant-in-Aid for Early-Career Scientists (No. 19K20658), and a Grant-in-Aid for JSPS Fellows (No. 20J21401) awarded by the Japan Society for the Promotion of Science. the Shimadzu Science Foundation, the Nakatani Foundation, the Kato Foundation for Promotion of Science, the Murata Science Foundation, and JST COI (No. JPMJCE1303).