Bernese Researchers Create Sophisticated Lung-on-chip (Medicine)

In collaboration with clinical partners from the Inselspital, researchers from the ARTORG Center for Biomedical Research of the University of Bern have developed a second-generation lung-on-chip model with life-size dimension alveoli in a stretchable membrane, made of purely biological material. The new model reproduces key aspects of the lung tissue architecture not found in previous lungs-on-chip. This opens up new possibilities for basic pneumological research, understanding lung pathologies, drug screening and precision medicine.

The lung is a complex organ whose main function is to exchange gases. It is the largest organ in the human body and plays a key role in the oxygenation of all the organs. Due to its structure, cellular composition and dynamic microenvironment, is difficult to mimic in vitro. 

A specialized laboratory of the ARTORG Center for Biomedical Engineering Research, University of Bern, headed by Olivier Guenat has developed a new generation of in-vitro models called organs-on-chip for over 10 years, focusing on modeling the lung and its diseases. After a first successful lung-on-chip system exhibiting essential features of the lung, the Organs-on-Chip (OOC) Technologies laboratory has now developed a purely biological next-generation lung-on-chip in collaboration with the Helmholtz Centre for Infection Research in Germany and the Thoracic Surgery and Pneumology Departments at Inselspital.

A fully biodegradable life-sized air-blood-barrier

Pauline Zamprogno, who developed the new model for her PhD thesis at the OOC, summarizes its characteristics: “The new lung-on-chip reproduces an array of alveoli with in vivo like dimensions. It is based on a thin, stretchable membrane, made with molecules naturally found in the lung: collagen and elastin. The membrane is stable, can be cultured on both sides for weeks, is biodegradable and its elastic properties allow mimicking respiratory motions by mechanically stretching the cells.”

Prof. Dr. Olivier Guenat, Head Organs-on-Chip Technologies, ARTORG Center for Biomedical Engineering Research, University of Bern. © Andres Burkhard / ARTORG Center for Biomedical Engineering

By contrast to the first generation, which was also built by the team around Olivier Guenat, the developed system reproduces key aspects of the lung extracellular matrix (ECM): Its composition (cells support made of ECM proteins), its structure (array of alveoli with dimension similar to those found in vivo + fiber structure) and its properties (biodegradability, a key aspect to investigating barrier remodeling during lung diseases such as IPF or COPD). Additionally, the fabrication process is simple and less cumbersome than that of a polydimethylsiloxane stretchable porous membrane from the first-generation lung-on-chip.

Broad potential clinical applications

Cells to be cultured on the new chip for research are currently obtained from cancer patients undergoing lung resections at the Inselspital Department of Thoracic Surgery. Department Head Ralph Schmid sees a double advantage in the system: “The second generation lung-on-chip can be seeded with either healthy or diseased lung alveolar cells. This provides clinicians with both a better understanding of the lung’s physiology and a predictive tool for drug screening and potentially also for precision medicine, identifying the specific therapy with the best potential of helping a particular patient.”

Dr. Pauline Zamprogno, PostDoc Organs-on-Chip Technologies, ARTORG Center for Biomedical Engineering Research, University of Bern. © zvg

“The applications for such membranes are broad, from basic science investigations into lung functionalities and pathologies, to identifying new pathways, and to a more efficient discovery of potential new therapies”, says Thomas Geiser, Head of the Department of Pneumology at the Inselspital and Director of Teaching and Research of the Insel Gruppe. 

Powerful alternative to animal models in research

As an additional plus, the new lung-on-chip can reduce the need for pneumological research based on animal models. “Many promising drug candidates successfully tested in preclinical models on rodents have failed when tested in humans due to differences between the species and in the expression of a lung disease,” explains Olivier Guenat. “This is why, in the long term, we aim to reduce animal testing and provide more patient-relevant systems for drug screening with the possibility of tailoring models to specific patients (by seeding organs-on-chip with their own cells).”

Pauline Zamprogno at the Organs-on-Chip Culture Laboratory of the ARTORG Center. © Adrian Moser

The new biological lung-on-chip will be further developed by Pauline Zamprogno and her colleagues from the OOC Technologies group to mimic a lung with idiopathic pulmonary fibrosis (IPF), a chronic disease of the lung leading to progressive scarring of the lung tissue within the framework of a research project funded by the Swiss 3R Competence Center (3RCC). “My new project consists in the development of an IPF-on- chip model based on the biological membrane. So far, we have develop a healthy air-blood barrier. Now it’s time to use it to investigate a real biological question,” says Zamprogno.

Video: The new lung-on-chip is a team development of the Organs-on-Chip Technologies of the ARTORG Center for Biomedical Engineering Research, University of Bern, with the Departments of Thoracic Surgery and Pneumology Inselspital, Bern University Hospital, and the Helmholtz Centre for Infection Research in Germany.

Video: This is how the new membrane works. © Artem Lopyrev / ARTORG Center for Biomedical Engineering Research

Featured image: Immunostaining of patients cell cultures on a second-generation lung-on-chip. © Pauline Zamprogno, ARTORG Center for Biological Engineering Research


Reference: Zamprogno, P., Wüthrich, S., Achenbach, S. et al.: Second-generation lung-on-a-chip with an array of stretchable alveoli made with a biological membrane. Commun Biol 4, 168 (2021). https://www.nature.com/articles/s42003-021-01695-0 https://doi.org/10.1038/s42003-021-01695-0


Provided by University of Bern

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