Researchers from the Deutsches Zentrum für Neurodegenerative Erkrankungen and the Center for Regenerative Therapies Dresden at TU Dresden have found that visual cells in the human retina may not simply die in some diseases, but are mechanically transported out of the retina beforehand.
During this process, the researchers filmed the organoids in real time by so-called live imaging, considered as the gold standard for cell tracking.
Visual cells in the human retina may not simply die in some diseases, but are mechanically transported out of the retina beforehand, according to researchers.
According to a news release, researchers from the Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE) and the Center for Regenerative Therapies Dresden (CRTD) at TU Dresden have now discovered this. For their research, they used miniature human retinas produced in the laboratory, so-called organoids.
The study1 was reported in the journal Nature Communications, with investigators noting it paves the way for completely new research approaches, especially in connection with age-related macular degeneration (AMD).
"This principle, known as cell extrusion, has not yet been studied in neurodegenerative diseases," said Mike Karl, PhD, who heads the research group. AMD is the main cause of blindness and severe visual impairment in Germany.
Researchers noted in the news release that it is estimated that a quarter of people over the age of 60 suffer from AMD. The macula is a special region within the human retina that is needed, among other things, for high resolution color vision. In AMD, thousands of light-sensitive visual cells, the so-called photoreceptor cells, are lost in the macula.
"This was the starting point for our research project: we observed that photoreceptors are lost, but we could not detect any cell death in the retina," said Karl, who conducts research at the Dresden site of the DZNE and the CRTD at TU Dresden. "Half of all photoreceptors disappeared from the retinal organoid within ten days, but obviously they did not die in the retina. That made us curious."
For the researchers - the DZNE and the CRTD were involved, as well as the Helmholtz Centre for Environmental Research (UFZ) - an elaborate search for the causes began. This led them to a study from 20122 in which Jody Rosenblatt, PhD, from King's College in London was the first to describe the extrusion of living cells - the mechanical ejection of cells from epithelia. The thereby extruded cells then only die in succession.
According to the news release, Rosenblatt demonstrated this mechanism in simple epithelial cells of the kidney. Karl and his team showed in their work that this extrusion can also be triggered in the much more complex retina, consisting of several different cell types, and leads to neurodegeneration. Interestingly, this cell extrusion could explain the outlying cells that have been previously reported in the ageing and diseased retina of patients with AMD and other diseases, but have not been studied in detail until now.
According to the researchers, they made use of a technique they had previously developed: They worked with so-called retinal organoids - an organ-like, three-dimensional model of the human retina grown from human stem cells in the laboratory. These organoids provide some characteristics of the human macula. The team found that two substances previously described in various neurodegenerative diseases - the proteins HBEGF and TNF - are sufficient to trigger degeneration in the retinal organoid.
During this process, the researchers filmed the organoids in real time by so-called live imaging, considered as the gold standard for cell tracking, according to the news release.
"We were able to capture the degeneration of photoreceptors through cell extrusion in the lab," Karl noted.
Moreover, the scientists found that this extrusion is triggered by activation of the protein PIEZO1, a sensor for biomechanical forces.
That biomechanics may play a larger role in retinal degeneration is a new finding.
"The retina is not known to be a biomechanically active tissue such as a muscle. It was known that diseases of the nervous system are associated with changes in the shape of cells, but to which extent biomechanical regulators are involved has not yet been studied in detail," Karl pointed out.
Thanks to the organoids, he and his team were able to observe the processes in an accelerated manner, so to speak: While it takes several years or even decades for photoreceptors to disappear in patients, such a process could now be reproduced in the laboratory in just 40 days. In the next step, the researchers now want to find out whether this mechanism occurs in human patients in the same way as in organoids. Initial findings suggest that this might be the same mechanism, but proof is still lacking.
In their study, the Dresden researchers also found that pharmacological agents could prevent extrusion in an experimental setting in their model. They used a special snake venom to block the mechanosensor PIEZO1 on the cells. As a result, not only were the photoreceptors not ejected, but further pathological changes in the retina were prevented.
"This gives hope for the development of future preventive and therapeutic treatments for complex neurodegenerative diseases such as AMD," Karl concluded.
1. Manuela Völkner, Felix Wagner, Lisa Maria Steinheuer, Madalena Carido, Thomas Kurth, Ali Yazbeck, Jana Schor, Stephanie Wieneke, Lynn J. A. Ebner, Claudia Del Toro Runzer, David Taborsky, Katja Zoschke, Marlen Vogt, Sebastian Canzler, Andreas Hermann, Shahryar Khattak, Jörg Hackermüller & Mike O. Karl: HBEGF-TNF induce a complex outer retinal pathology with photoreceptor cell extrusion in human organoids. Nature Communications. Published October 2022. DOI: 10.1038/s41467-022-33848-y
2. George T. Eisenhoffer, Patrick D. Loftus, Masaaki Yoshigi, Hideo Otsuna, Chi-Bun Chien, Paul A. Morcos, and Jody Rosenblatt. Crowding induces live cell extrusion to maintain homeostatic cell numbers in epithelia. Nature. Published April 15, 2012. doi: 10.1038/nature10999